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	<updated>2026-09-23T05:41:22Z</updated>
	<subtitle>User contributions</subtitle>
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		<id>https://proteopedia.org/index.php?title=Print3D_models_gallery&amp;diff=4396894</id>
		<title>Print3D models gallery</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_models_gallery&amp;diff=4396894"/>
		<updated>2025-12-01T08:52:18Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Welcome to the Proteopedia gallery of 3D printed models==&lt;br /&gt;
&lt;br /&gt;
Did you use the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in Proteopedia to create a printable model? &lt;br /&gt;
&lt;br /&gt;
Do you have pictures of the final 3D printed model of a molecule? &lt;br /&gt;
&lt;br /&gt;
Or better, do you have a picture of the model put to good use? &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;We would love to know more about it&#039;&#039;&#039;. Please feel free to contribute to this page and share your prints!  Note: If editing this page it&#039;s not for you and you would prefer to focus on 3D printing, drop us an e-mail at marius.mihasan(@)uaic.ro and we would love to hear your story and share it on this page. &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Picture&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Details (including link to Proteopedia page if possible)&lt;br /&gt;
|-&lt;br /&gt;
| A simplified model of SV40 Capsid&lt;br /&gt;
|[[Image:SV40_Capsid_3DPrinted.jpg|400px|center|thumb| SV40 Capsid, [[SV40_Capsid_Simplified]]]]&lt;br /&gt;
|Model of SV40 Capsid printed on multi-material printer (Bambulab A1 Mini). Printable files available on [https://www.printables.com/model/1308340-a-simplified-model-of-sv40-capsid Printables.com]. Generated with the Proteopedia Print3D tool from [[SV40_Capsid_Simplified]]. Printed by [[User:Marius Mihasan|Marius Mihasan]] 12:27, 8 October 2025 (UTC).&lt;br /&gt;
|-&lt;br /&gt;
| GABBA receptor&lt;br /&gt;
|[[Image:GABAA_receptor.png|400px|center|thumb| GABAA receptor, [[6x3x]]]]&lt;br /&gt;
|Trace Model of the GABAA receptor [[6x3x]] printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com]. Printed by [[User:Marius Mihasan|Marius Mihasan]] 12:27, 8 October 2025 (UTC)&lt;br /&gt;
|-&lt;br /&gt;
|Model 3  &lt;br /&gt;
|Image with model 3&lt;br /&gt;
|Description of model 3&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4396893</id>
		<title>Print3D help</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4396893"/>
		<updated>2025-12-01T08:52:00Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== Proteopedia and 3D Printing ==&lt;br /&gt;
&lt;br /&gt;
Physical molecular models, by engaging both visual and tactile senses, provide an effective means of deepening the understanding of complex concepts in molecular biology and biochemistry. They allow students to perceive the three-dimensional organization of macromolecules, thereby enhancing comprehension of the relationship between structure and function &amp;lt;ref&amp;gt;PMID: 32590880&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 40214166&amp;lt;/ref&amp;gt;. Numerous studies have demonstrated that the use of tangible models in science education improves learning outcomes, fosters conceptual reasoning, and increases student engagement &amp;lt;ref&amp;gt;PMID: 27366318&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 26712513&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;Larsson, C., Tibell, L.A.E. Challenging Students’ Intuitions—the Influence of a Tangible Model of Virus Assembly on Students’ Conceptual Reasoning About the Process of Self-Assembly. Res Sci Educ 45, 663–690 (2015). [http://dx.doi.org/10.1007/s11165-014-9446-6 DOI: 110.1007/s11165-014-9446-6]&amp;lt;/ref&amp;gt;. The rapid development of 3D-printing technologies has made it possible to create customized and affordable molecular models  &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot;&amp;gt;PMID: 28362403&amp;lt;/ref&amp;gt; &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot;&amp;gt;PMID: 33755300&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 33384761&amp;lt;/ref&amp;gt;. &lt;br /&gt;
&lt;br /&gt;
Affordable desktop 3D printers can now be used to fabricate physical models from virtually any structure or scene on [[Proteopedia]]. This page provides an introduction to 3D printing, a step-by-step guide to generating printable files directly from [[Proteopedia]], and several tested printing profiles for common printers (e.g., Prusa Research, Bambu Lab, Creality, or Elegoo).&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== «3D Printing 101»: an introduction to 3D printing ==&lt;br /&gt;
3D printing, also known as &#039;&#039;additive manufacturing&#039;&#039;, builds physical objects layer by layer from digital designs. For more technical details please head for the excellent introductory article on [https://all3dp.com/2/what-is-3d-printing/ All3DP].  In structural biology education, 3D printing provides an affordable and accessible way to transform atomic coordinate data (e.g., from PDB, MOL or SDF files) into tangible molecular models that can be observed, handled, and discussed in class or laboratory settings.&lt;br /&gt;
&lt;br /&gt;
=== Printer Types: FDM vs. SLA/DLP ===&lt;br /&gt;
The two most accessible 3D-printing technologies that can be used to create molecular models are:&lt;br /&gt;
* &#039;&#039;&#039;FDM (Fused Deposition Modeling)&#039;&#039;&#039;&lt;br /&gt;
This method extrudes a heated thermoplastic filament (such as PLA, PETG or TPU) through a fine nozzle, depositing successive layers that form the model. FDM printers have the advantages of low cost, easy maintenance, wide availability, and being capable of printing large and colorful molecular models. This technology has a few limitations, such as: visible layer lines, lower surface resolution, and less suited for very small or intricate molecular details.&lt;br /&gt;
* &#039;&#039;&#039;SLA/DLP (Resin Printing)&#039;&#039;&#039;&lt;br /&gt;
This technique uses liquid photopolymer resin, cured layer by layer with ultraviolet light. SLA/DLP printers have the advantages of a very high resolution, smooth surfaces and are ideal for compact and detailed models (e.g., small proteins rendered as surface, ligands, or symmetric assemblies). This technology has its own limitations, such as higher material cost, post-processing requirements (washing and UV-curing), and the need for careful handling of resin.&lt;br /&gt;
&lt;br /&gt;
When choosing between FDM and SLA printers, model size and resolution are the key criteria: &#039;&#039;&#039;FDM&#039;&#039;&#039; is preferred for &#039;&#039;large, educational display models&#039;&#039;; &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; is optimal for &#039;&#039;small, precise structures&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
While FDM and SLA/DLP are the most widely used technologies in educational and research contexts due to their accessibility, other additive manufacturing methods also exist —such as &#039;&#039;Selective Laser Sintering&#039;&#039; (SLS), &#039;&#039;PolyJet&#039;&#039;, and &#039;&#039;Binder Jetting&#039;&#039;— each employing different materials and curing mechanisms. These industrial-grade techniques can produce highly detailed or multi-material parts but are generally more expensive and less accessible for classroom use. For an overview of major 3D-printing technologies, see [https://all3dp.com/1/types-of-3d-printers-3d-printing-technology/ All3DP: Complete Overview of the Types of 3D Printers]&lt;br /&gt;
&lt;br /&gt;
=== Single- vs. Multi-Material Printers ===&lt;br /&gt;
Most entry-level desktop 3D printers use a single filament or resin, producing models in one color or material. However, multi-material systems (such as [https://eu.store.bambulab.com/products/ams-multicolor-printing?from=home_web_top_navigation Bambu Lab AMS] and its variants or [https://www.prusa3d.com/category/original-prusa-mmu3/ Prusa MMU3]) can simultaneously print multiple filaments, enabling color-coded domains, subunits, or ligands directly in one print. For complex color information, users can also apply post-print color coding (painting or labeling) or print separate parts and assemble them manually.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A large FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A multi-material FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Small resin-printed models&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:GABAA_receptor.png|320px|center|thumb| GABAA receptor, [[6x3x]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Bacterial_Ribosome_multimaterial_FDM.png|348px|center|thumb| Bacterial 70S ribosome, [[4v5d]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Dna_insuline_sla.png|252px|center|thumb|DNA (left) and insulin (right) models, [[4bna]] and [[4ins]], scale at the bottom in cm]]&lt;br /&gt;
|-&lt;br /&gt;
|Trace Model of the GABAA receptor printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com] &lt;br /&gt;
|Surface model of the Bacterial 70S ribosome printed on a multi-material capable printer (BambuLab X1C AMS). Blue and violet are ribosomal proteins, orange and yellow are rRNAs, and black is tRNA. Printable files available on [https://www.printables.com/model/1430877-bacterial-70s-ribosome Printables.com]&lt;br /&gt;
|Balls and sticks and cartoon models of DNA (right) and insulin (left)&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== File Formats Used in 3D Printing ===&lt;br /&gt;
Proteopedia supports two export formats for generating printable molecular models:&lt;br /&gt;
*&#039;&#039;&#039;.STL&#039;&#039;&#039; (Stereolithography): the most common and universally compatible format; encodes only surface geometry, without color or texture information.&lt;br /&gt;
*&#039;&#039;&#039;.OBJ&#039;&#039;&#039; (Wavefront Object) with an associated &#039;&#039;&#039;.MTL&#039;&#039;&#039; (Material Template Library) files: includes both geometry and optional color/texture data; useful for color prints.&lt;br /&gt;
&lt;br /&gt;
Another widely adopted file format used in 3D printing is the &#039;&#039;&#039;.3MF&#039;&#039;&#039; (3D Manufacturing Format): a modern open standard that stores geometry, color, and multi-material metadata in a single file—recommended for advanced printers. For a more extensive pros and cons of different 3D printing file formats please see [https://all3dp.com/2/3d-file-format-3d-model-types/ The Main 3D Printing File Formats on all3dp]. &lt;br /&gt;
&lt;br /&gt;
STL is ideal for single-color models and maximum compatibility, while OBJ/MTL is recommended for multi-material workflows. 3MF files will be used in this tutorial to save the model and printing settings. &lt;br /&gt;
&lt;br /&gt;
Support in Proteopedia for these formats is based on the export capabilities of Jmol/JSmol; for details, see [http://wiki.jmol.org/index.php/File_formats/3D_Objects#STL STL] and [http://wiki.jmol.org/index.php/File_formats/3D_Objects#OBJ OBJ]&lt;br /&gt;
&lt;br /&gt;
== Overview of the 3D printing process ==&lt;br /&gt;
3D printing enables the transformation of atomic-level structural data into tangible macromolecular models that can be explored through both sight and touch.  &lt;br /&gt;
The process generally follows several main steps, each requiring specific types of software and hardware.&lt;br /&gt;
[[Image:3D_printing_workflow_v2.png|thumb|left|400px|Overview of the 3D printing workflow for generating physical molecular models.]]&lt;br /&gt;
	&lt;br /&gt;
=== Preparing the structure and generating a printable File ===&lt;br /&gt;
:The first stage involves creating a printable three-dimensional representation of the molecule. Some molecular-graphics programs such as [https://www.pymol.org/ PyMOL], [https://www.rbvi.ucsf.edu/chimerax/ UCSF ChimeraX], [https://molstar.org/Mol*], or [https://jmol.sourceforge.net/ Jmol] can be used not only to visualize a structure (from the Protein Data Bank or other sources), but also to export the resulting geometry in a .STL or .OBJ format. However, the default visualization styles of these programs are &#039;&#039;&#039;&#039;&#039;not directly suitable for 3D printing&#039;&#039;&#039;&#039;&#039;. Therefore, when preparing a model for fabrication, it is important to:&lt;br /&gt;
:* &#039;&#039;&#039;Select an appropriate molecular representation&#039;&#039;&#039; (e.g., surface, cartoon, sticks, spheres) depending on the pedagogical or structural feature you wish to highlight.  &lt;br /&gt;
:* &#039;&#039;&#039;Add struts or connectors&#039;&#039;&#039; to increase the mechanical stability of the model, especially for large complexes or long helices.  &lt;br /&gt;
:* &#039;&#039;&#039;Remove specific struts or pseudobonds&#039;&#039;&#039; when individual components — ligands, subunits, or cofactors — need to remain detachable.  &lt;br /&gt;
:* &#039;&#039;&#039;Adjust thickness&#039;&#039;&#039; of atoms, bonds, helices, and sheets to ensure adequate rigidity and printability (features thinner than the printer’s nozzle diameter or resin resolution may break).  &lt;br /&gt;
:* &#039;&#039;&#039;Apply meaningful coloring&#039;&#039;&#039; when preparing multi-material prints, for instance, to distinguish domains, chains, ligands or atoms.&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene that automates the process and enables users to effortlessly generate 3D-printable molecular models - more on that in the corresponding section [[#Generating printable files on Proteopedia|Generating printable files on Proteopedia]] within this page. For advanced users wanting to do this manually, we highly recommend two guides: &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot; /&amp;gt; and &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
=== Slicing the Model ===&lt;br /&gt;
Before printing, the STL file must be processed by a &#039;&#039;&#039;slicer&#039;&#039;&#039; — specialized software that converts 3D geometry into a series of horizontal layers. The slicer also generates &#039;&#039;&#039;G-code&#039;&#039;&#039;, the set of instructions that control the printer. These commands are printer-specific and include parameters such as extrusion speed, layer thickness, temperature, and movement. Together, they are usually stored as a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;.  &lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an FDM printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;number of perimeters&#039;&#039;&#039;, which affects mechanical strength and print time;&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines resolution and print duration;&lt;br /&gt;
:* &#039;&#039;&#039;infill density&#039;&#039;&#039;, which determines internal strength and affects print time;&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, temporary structures that hold overhanging regions;&lt;br /&gt;
:* &#039;&#039;&#039;print orientation&#039;&#039;&#039;, which influences surface quality, mechanical strength, and the amount of supports required.&lt;br /&gt;
:All these parameters make up a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. In this step, users must also select the material-specific parameters, or apply a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. More details on these profiles are provided later on this page.&lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines vertical resolution and print time; thinner layers produce smoother surfaces but significantly increase printing duration.&lt;br /&gt;
:* &#039;&#039;&#039;exposure time&#039;&#039;&#039;, which controls how long each layer is cured by UV light; optimal exposure ensures proper adhesion between layers without over-curing fine details.&lt;br /&gt;
:* &#039;&#039;&#039;bottom-layer exposure and count&#039;&#039;&#039;, which influence model adhesion to the build platform — longer exposures and additional base layers improve stability during printing.&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, which anchor the model to the build plate and prevent deformation during peeling; proper placement reduces surface marks and print failures.&lt;br /&gt;
:* &#039;&#039;&#039;model orientation&#039;&#039;&#039;, which affects surface quality, support contact area, and resin drainage; angling the model (typically 30–45°) minimizes suction forces and improves print reliability.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for FDM printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for resin printing&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:Insuline_sliced_prusa.gif|386px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|[[Image:Insuline_Sliced_SLA.gif|372px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|-&lt;br /&gt;
|Cartoon model of insulin sliced in PrusaSlicer and ready to be printed on FDM printers. The arrow shows the trajectory of the print head on a single slice or layer. Orange is the model, green are the supports. &lt;br /&gt;
|Cartoon model of insulin sliced in Elegoo SatelLite and ready to be printed on FDM printer.On the left, with blue is the model, with gray are the supports. On the right is the image on the UV screen. &lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== 3D Printing the Model ===&lt;br /&gt;
:The prepared G-code is then transferred to the 3D printer, either via an SD card, USB flash drive, or Wi-Fi connection. During printing, close observation of the first few layers is essential to ensure good adhesion to the build plate and a successful print. Total printing time depends on model size, selected layer height, and printer speed. &#039;&#039;Small peptide&#039;&#039; models may print in &#039;&#039;&#039;less than an hour&#039;&#039;&#039;, whereas l&#039;&#039;arge multimeric assemblies&#039;&#039; can require &#039;&#039;&#039;several hours or days&#039;&#039;&#039;. &#039;&#039;Multi-color&#039;&#039; or &#039;&#039;multi-material&#039;&#039; prints generally take &#039;&#039;&#039;longer&#039;&#039;&#039;, while &#039;&#039;SLA/DLP&#039;&#039; printers are generally &#039;&#039;&#039;faster&#039;&#039;&#039; due to their simultaneous layer exposure.&lt;br /&gt;
=== Post-Processing ===&lt;br /&gt;
:After printing, the model undergoes post-processing, which varies depending on the printing technology used:&lt;br /&gt;
:* For &#039;&#039;&#039;FDM prints&#039;&#039;&#039;, supports are removed mechanically, and surfaces can be smoothed by light sanding or polishing.&lt;br /&gt;
:* For &#039;&#039;&#039;resin prints&#039;&#039;&#039;, supports are removed mechanically, parts are washed in isopropanol to remove uncured resin and then exposed to UV light for final curing.&lt;br /&gt;
:Models printed in multiple parts can be assembled using cyanoacrylate or epoxy adhesive. Optional finishing steps (painting, labeling) can improve contrast between subunits or highlight functional regions.&lt;br /&gt;
&lt;br /&gt;
==Generating printable files on Proteopedia==&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene, enabling logged-in users to effortlessly generate 3D-printable molecular models directly from its pages. The tool is powered by [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;], a script that analyzes the structural data and automatically scales the model’s geometry to match the printable volume of a medium-size desktop 3D printer (e.g., Ender-3, 210×210×210 mm). During this process, the tool evaluates the molecular bounding box, atom radii, and bond lengths, then proportionally adjusts all dimensions to achieve a realistic and mechanically robust print scale — preserving scientific accuracy while ensuring manufacturability. For advanced users, [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;] may also be used in conjunction with the [https://jmol.sourceforge.net/ &#039;&#039;&#039;Jmol&#039;&#039;&#039;] program, providing full access to its scripting capabilities and advanced export features.&lt;br /&gt;
==Step-by-step guide for automatic generation of printable files on Proteopedia==&lt;br /&gt;
=== Open a structure and access the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool ===&lt;br /&gt;
Log in with your Proteopedia Username and password. Navigate to any Proteopedia page (for example, [[Introduction_to_protein_structure]]). The corresponding 3D structure will load in the viewer on the right.  &lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_button_in_Proteopedia.png|thumb|left|400px|The &#039;&#039;&#039;Print3D&#039;&#039;&#039; button on a Proteopedia page]]&lt;br /&gt;
&lt;br /&gt;
At the bottom of the structure display window, locate and click the &#039;&#039;&#039;Print3D&#039;&#039;&#039; button. The tool will launch and begin analyzing the current molecular structure.  &lt;br /&gt;
This process may take some time to complete, depending on the size of the structure.  &lt;br /&gt;
Please wait until the message &#039;&#039;&#039;Analyzing structure...&#039;&#039;&#039; disappears and the next page is displayed — this marks the start of the two-step printing workflow.&lt;br /&gt;
=== Select a molecular representation and a printing scale ===&lt;br /&gt;
In this new page, some user input is required. Each option includes a short explanation; the key steps are outlined below, but feel free to explore and adopt the settings that best fit your use case.&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step1.png|thumb|left|400px|Selecting molecular representation and printing scale]]&lt;br /&gt;
&lt;br /&gt;
(1) &#039;&#039;&#039;Choose a molecular representation&#039;&#039;&#039; from the &#039;&#039;&#039;Scheme&#039;&#039;&#039; list, based on your goal:&lt;br /&gt;
* &#039;&#039;&#039;Backbone&#039;&#039;&#039;, &#039;&#039;&#039;Trace&#039;&#039;&#039;, or &#039;&#039;&#039;Ribbon&#039;&#039;&#039; — to emphasize secondary structure (effective for teaching protein folds).&lt;br /&gt;
* &#039;&#039;&#039;Surface&#039;&#039;&#039; — to highlight molecular topology and binding sites.&lt;br /&gt;
* &#039;&#039;&#039;Ball &amp;amp; Stick&#039;&#039;&#039; — atom-level detail for ligands or small molecules; usually impractical for large proteins or complexes.&lt;br /&gt;
* &#039;&#039;&#039;Proteopedia Scene&#039;&#039;&#039; — attempts to render the current page’s scene directly; may not work for all scenes. This is not fully implemented and only available for a few users.&lt;br /&gt;
&#039;&#039;Note:&#039;&#039; Some representations may be unavailable for a given structure because they are not printable in a reliable way.&lt;br /&gt;
&lt;br /&gt;
(2) In the &#039;&#039;&#039;Printer&#039;&#039;&#039; section, select whether you want a &#039;&#039;&#039;single-color&#039;&#039;&#039; or a &#039;&#039;&#039;multi-color&#039;&#039;&#039; print.&lt;br /&gt;
&lt;br /&gt;
(3) In the &#039;&#039;&#039;Printer scale&#039;&#039;&#039; section, set the desired size of the printed model. The tool constrains safe sizes based on the chosen representation and displays the physical dimensions (mm). &#039;&#039;&#039;Important! Please note the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;printer scale value in %&amp;lt;/span&amp;gt; as it is going to be required downstream in the next section of this workflow, [[#Printing files from Proteopedia|Printing files from Proteopedia]]&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
(4) When ready, click the green &#039;&#039;&#039;Make printer files&#039;&#039;&#039; button. Please wait patiently until the  &#039;&#039;Generating files for 3D printing of...&#039;&#039; message disappears and the final step is displayed.&lt;br /&gt;
&lt;br /&gt;
===Download the .STL or .OBJ files===&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step2.png|thumb|left|400px|Final step in generating printable files]]&lt;br /&gt;
&lt;br /&gt;
In this final page, a 3D preview of the generated model is displayed.&lt;br /&gt;
You can use the mouse to rotate, zoom, and inspect the model from different angles. If the result meets your needs, click the green (A) &#039;&#039;&#039;Download files&#039;&#039;&#039; button and save the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive containing the &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; files on your computer. If your model needs further improvements, hit the green (B) &#039;&#039;&#039;Same structure&#039;&#039;&#039; button to return to the previous screen and adjust your settings.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{clear}}&lt;br /&gt;
== Printing files from Proteopedia ==&lt;br /&gt;
Unzipping the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive will produce the exported &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file, along with an optional &#039;&#039;&#039;.MTL&#039;&#039;&#039; material file. &lt;br /&gt;
=== Using 3D printing services ===&lt;br /&gt;
If you do not have a 3D printer, you can still obtain physical models by using locally available 3D-printing services. Just search on [https://www.google.com/maps Google Maps] with the term  &#039;&#039;&#039;3D printing&#039;&#039;&#039; in your area. Here is short list of well-known 3D Printing service providers that may also ship worldwide: &lt;br /&gt;
&lt;br /&gt;
* [https://www.shapeways.com/ &#039;&#039;&#039;Shapeways&#039;&#039;&#039;] — global service offering a wide range of materials and colors. Educational discounts are available through their academic program.&lt;br /&gt;
* [https://www.sculpteo.com/en/ &#039;&#039;&#039;Sculpteo&#039;&#039;&#039;] — Europe-based provider offering fast turnaround and many printing technologies, including resin and polymer options.&lt;br /&gt;
* [https://www.xometry.com/capabilities/3d-printing-service &#039;&#039;&#039;Xometry&#039;&#039;&#039;] — large international network providing access to industrial-grade printing methods such as FDM, SLA, SLS, and DMLS.&lt;br /&gt;
* [https://craftcloud3d.com/ &#039;&#039;&#039;Craftcloud&#039;&#039;&#039;] — an aggregator that compares multiple providers and finds the best price and lead time for your uploaded model.&lt;br /&gt;
&lt;br /&gt;
When contacting a printing service, provide the exported files together with the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value in %&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ([[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). It is also advisable to share the link to this Proteopedia page so that the operator understands the peculiarities of printing molecular models. &lt;br /&gt;
&lt;br /&gt;
=== Using a desktop 3D printer ===&lt;br /&gt;
&lt;br /&gt;
Before importing the .STL or .OBJ file into your slicer software, it is recommended to inspect and, if necessary, repair the model to ensure printability. Common issues include non-manifold geometry, intersecting faces, and missing surfaces.  The example below demonstrates how to use [https://www.blender.org/ &#039;&#039;&#039;Blender&#039;&#039;&#039;] together with its [https://extensions.blender.org/add-ons/print3d-toolbox/ &#039;&#039;&#039;3D Print Toolbox extension&#039;&#039;&#039;] to improve the printability of the .STL and .OBJ files generated with the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in [[Proteopedia]]. &#039;&#039;&#039;Important note&#039;&#039;&#039;: The repair process is largely automated but may introduce artifacts. Carefully inspect the corrected model for any missing or distorted sections, atoms, or bonds, and determine whether these omissions affect the intended purpose of the printed model.  &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for single color or resin printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for multi-color FDM printing&lt;br /&gt;
|-&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=k6u-5JnoP-c&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=OCisrIZMIDM&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|}  &lt;br /&gt;
&lt;br /&gt;
Once the repaired &#039;&#039;&#039;.STL or .OBJ&#039;&#039;&#039; file is ready, it can be imported into your slicer software. In this step, you will prepare the file for printing by applying appropriate printer, filament, and print-settings profiles.&lt;br /&gt;
&lt;br /&gt;
*Apply the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value (%)&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ( [[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). This step ensures that the model fits your print bed and maintains structural integrity during printing. The location of the scale (%) input field varies depending on the slicer software you are using.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Orient the model on the print bed&#039;&#039;&#039; so that its largest, flattest surface rests on the bed. This minimizes the need for supports and improves adhesion. If your slicer includes an Auto Orient or Auto Arrange function, use it to optimize placement. (&#039;&#039;Hint&#039;&#039;: Bambu Studio and Orca Slicer include this feature, Ultimaker Cura has a [https://marketplace.ultimaker.com/app/cura/plugins/nallath/OrientationPlugin Auto-Orientation plugin] available, while PrusaSlicer currently does not.)&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Select the printer&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that matches your device.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Choose the material&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; corresponding to the filament type (e.g., PLA, PETG, TPU) and manufacturer you intend to use.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Adjust the printing parameters&#039;&#039;&#039; by selecting a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that defines layer height, infill, speed, and support options.&lt;br /&gt;
&lt;br /&gt;
In most cases, the default &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; and &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; provided by the slicer are sufficient. However, molecular models often include overhangs, thin connections, and complex internal geometries, which require additional supports and reinforced perimeters to ensure structural stability. For this reason, the default &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; may not yield optimal results.&lt;br /&gt;
&lt;br /&gt;
Validated printing profiles for the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool are available for several printer models. These profiles provide optimized settings that produce sturdy models, reduce material consumption, and shorten print time, ensuring consistent and reliable results. Three distinct profiles are supplied, corresponding to major molecular representations: &#039;&#039;&#039;balls and sticks&#039;&#039;&#039;, &#039;&#039;&#039;surface&#039;&#039;&#039;, and &#039;&#039;&#039;cartoon&#039;&#039;&#039;. The &#039;&#039;&#039;cartoon&#039;&#039;&#039; profile is also suitable for &#039;&#039;&#039;backbone&#039;&#039;&#039;, &#039;&#039;&#039;trace&#039;&#039;&#039;, and &#039;&#039;&#039;ribbon&#039;&#039;&#039; representations. For some printers, each profile is supplied in two variants, one using standard supports and one using tree or organic supports. In the case of multi-material printers, profiles for printing with soluble support and soluble interface are also provided.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer brand and model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Profiles provided as / Slicer&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer Type, nozle size and multi-material support&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |GitHub with profiles&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to import profiles into Slicer&lt;br /&gt;
|-&lt;br /&gt;
|Original Prusa Core One&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer ]&lt;br /&gt;
|FDM / 0.4 mm / yes, 5 colors, if MMU3 installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/Prusa%20CoreOne CoreOne]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab A1Mini&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, 4 colors if AMS Lite is installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/BambuLab%20A1Mini AiMini]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab X1 Carbon&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, up to 16 colors if multiple AMS are installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ca92e7de9c72505c1b9b09e912ad177341cabc9a/BambuLab%20X1C X1Carbon]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|- &lt;br /&gt;
|Original Prusa MK3S+&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/7a7ee68d1e19f063600f53def49a99dfefbc595d/Prusa%20MK3S%2B MK3S+]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 5 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/a653c7cc6b3dec86b90117cc450d1883cc4a80bd/Ender-5-Pro Ender5Pro]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 3 v2 with a ENDERIDEX kit&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / yes, IDEX, two filaments&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/c2c74f1261a42c160e7e3898a407f21465de2ca7/Ender3-IDEX Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Kingroon KPS3 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ea733b2d05020b99f91c92f71a039c5ba8e54108/Kingroon-KPS3-Pro Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Elegoo Mars 5 Ultra&lt;br /&gt;
|no profile needed, just be sure to add supports / [https://www.elegoo.com/pages/satellite-3d-slicer?srsltid=AfmBOopMQGHgHycHMFOZALzOIC8z7bVlSHjL_jj2ShYR4QkowYKmKzUx ELEGOO SatelLite]&lt;br /&gt;
|resin / - / no&lt;br /&gt;
|&lt;br /&gt;
|no profile needed, default settings worked, just be sure to add supports. EVO supports worked well enough.  Post-processing steps: 1)washing: at least 10 min. 2) support removal 3)curring: at least 10 min on a Elegoo Mercury Plus V3.0&lt;br /&gt;
|- &lt;br /&gt;
|} &lt;br /&gt;
&#039;&#039;&#039;Notes&#039;&#039;&#039;: &lt;br /&gt;
* These profiles were developed and validated with the support of EDUMOL3D, Project [http://cercetare.bio.uaic.ro/grupuri/bioactive/content/grants/PED2024_mm.html PN-IV-P7-7.1-PED-2024-0343] financed by the Ministry of Research, Innovation and Digitization, [https://uefiscdi.gov.ro/ UEFISCDI], Romania.&lt;br /&gt;
* The profiles are a work in progress. Please check GitHub for updates. If you have suggestions for improvements, please drop a message at marius.mihasan(@)uaic.ro&lt;br /&gt;
&lt;br /&gt;
==== &#039;&#039;&#039;Note on multi-color printing &#039;&#039;&#039; ====&lt;br /&gt;
To our knowledge, only &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039; and &#039;&#039;&#039;Orca Slicer&#039;&#039;&#039; can automatically import color information from the &#039;&#039;&#039;.MTL&#039;&#039;&#039; file associated with the printable &#039;&#039;&#039;.OBJ&#039;&#039;&#039; generated by the Proteopedia &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool.  &lt;br /&gt;
At present, &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; does not support importing &#039;&#039;&#039;.MTL&#039;&#039;&#039; files directly.&lt;br /&gt;
&lt;br /&gt;
A practical workaround for &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; users is as follows:  &lt;br /&gt;
# Open the &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file in &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039;.  &lt;br /&gt;
#Verify or adjust the color mapping as needed.  &lt;br /&gt;
#Export the model as a generic &#039;&#039;&#039;.3MF&#039;&#039;&#039; file using the menu command:  &#039;&#039;File&#039;&#039; → &#039;&#039;Export&#039;&#039; → &#039;&#039;Export Generic 3MF...&#039;&#039;  &lt;br /&gt;
#Open the exported &#039;&#039;&#039;.3MF&#039;&#039;&#039; file in &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;. The color data will now be available under the &#039;&#039;&#039;Multimaterial Painting&#039;&#039;&#039; tool.&lt;br /&gt;
&lt;br /&gt;
This workflow preserves the original coloring assigned in Proteopedia and allows successful multi-color or multi-material printing on any capable 3D printer compatible with &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Other relevant resources ==&lt;br /&gt;
[https://proteopedia.org/w/Print3D_models_gallery Print3D Models gallery] - examples of 3D printed molecular models from Proteopedia users.&lt;br /&gt;
&lt;br /&gt;
[https://3d.nih.gov/ NIH 3D Print Exchange] - an open, community-driven portal to download, share, and create bioscientific and medical 3D models, including for 3D printing.&lt;br /&gt;
  &lt;br /&gt;
[https://github.com/mariusmihasan/3DP-Jmol 3DP-Jmol] - the Jmol/JSmol behind the Print3D tool. Automatically generates 3D printable molecular models from structural data and can be easily integrated into web pages.&lt;br /&gt;
&lt;br /&gt;
[https://pdb101.rcsb.org/learn/3d-printing/pdb-structures-and-3d-printing 3D Printing on PDB101] - a quick guide on 3D printing molecular models and a small curated 3D models for education&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;If you print a model from Proteopedia, please share photos and feedback — let’s 3D print the whole Proteopedia!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Print3D_models_gallery&amp;diff=4396892</id>
		<title>Print3D models gallery</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_models_gallery&amp;diff=4396892"/>
		<updated>2025-12-01T08:50:31Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Welcome to the Proteopedia gallery of 3D printed models==&lt;br /&gt;
&lt;br /&gt;
Did you use the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in Proteopedia to create a printable model? &lt;br /&gt;
&lt;br /&gt;
Do you have pictures of the final 3D printed model of a molecule? &lt;br /&gt;
&lt;br /&gt;
Or better, do you have a picture of the model put to good use? &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;We would love to know more about it&#039;&#039;&#039;. Please feel free to contribute to this page and share your prints!  Note: If editing this page it&#039;s not for you and you would prefer to focus on 3D printing, drop us an e-mail at marius.mihasan(@)uaic.ro and we would love to hear your story and share it on this page. &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Picture&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Details (including link to Proteopedia page if possible)&lt;br /&gt;
|-&lt;br /&gt;
| A simplified model of SV40 Capsid&lt;br /&gt;
|[[Image:SV40_Capsid_3DPrinted.jpg|400px|center|thumb| SV40 Capsid, [[SV40_Capsid_Simplified]]]]&lt;br /&gt;
|Model of SV40 Capsid printed on multi-material printer (Bambulab A1 Mini). Printable files available on [https://www.printables.com/model/1308340-a-simplified-model-of-sv40-capsid Printables.com]. Generated with the Proteopedia Print3D tool from [[SV40_Capsid_Simplified]]. Printed by [[User:Marius Mihasan|Marius Mihasan]] 12:27, 8 October 2025 (UTC).&lt;br /&gt;
|-&lt;br /&gt;
| GABBA receptor&lt;br /&gt;
|[[Image:GABAA_receptor.png|400px|center|thumb| GABAA receptor, [[6x3x]]]]&lt;br /&gt;
|Trace Model of the GABAA receptor [[6x3x]] printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com]. Printed by [[User:Marius Mihasan|Marius Mihasan]] 12:27, 8 October 2025 (UTC)&lt;br /&gt;
|-&lt;br /&gt;
|Model 3  &lt;br /&gt;
|Image with model 3&lt;br /&gt;
|Description of model 3&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4396891</id>
		<title>Print3D help</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4396891"/>
		<updated>2025-12-01T08:50:10Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== Proteopedia and 3D Printing ==&lt;br /&gt;
&lt;br /&gt;
Physical molecular models, by engaging both visual and tactile senses, provide an effective means of deepening the understanding of complex concepts in molecular biology and biochemistry. They allow students to perceive the three-dimensional organization of macromolecules, thereby enhancing comprehension of the relationship between structure and function &amp;lt;ref&amp;gt;PMID: 32590880&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 40214166&amp;lt;/ref&amp;gt;. Numerous studies have demonstrated that the use of tangible models in science education improves learning outcomes, fosters conceptual reasoning, and increases student engagement &amp;lt;ref&amp;gt;PMID: 27366318&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 26712513&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;Larsson, C., Tibell, L.A.E. Challenging Students’ Intuitions—the Influence of a Tangible Model of Virus Assembly on Students’ Conceptual Reasoning About the Process of Self-Assembly. Res Sci Educ 45, 663–690 (2015). [http://dx.doi.org/10.1007/s11165-014-9446-6 DOI: 110.1007/s11165-014-9446-6]&amp;lt;/ref&amp;gt;. The rapid development of 3D-printing technologies has made it possible to create customized and affordable molecular models  &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot;&amp;gt;PMID: 28362403&amp;lt;/ref&amp;gt; &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot;&amp;gt;PMID: 33755300&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 33384761&amp;lt;/ref&amp;gt;. &lt;br /&gt;
&lt;br /&gt;
Affordable desktop 3D printers can now be used to fabricate physical models from virtually any structure or scene on [[Proteopedia]]. This page provides an introduction to 3D printing, a step-by-step guide to generating printable files directly from [[Proteopedia]], and several tested printing profiles for common printers (e.g., Prusa Research, Bambu Lab, Creality, or Elegoo).&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== «3D Printing 101»: an introduction to 3D printing ==&lt;br /&gt;
3D printing, also known as &#039;&#039;additive manufacturing&#039;&#039;, builds physical objects layer by layer from digital designs. For more technical details please head for the excellent introductory article on [https://all3dp.com/2/what-is-3d-printing/ All3DP].  In structural biology education, 3D printing provides an affordable and accessible way to transform atomic coordinate data (e.g., from PDB, MOL or SDF files) into tangible molecular models that can be observed, handled, and discussed in class or laboratory settings.&lt;br /&gt;
&lt;br /&gt;
=== Printer Types: FDM vs. SLA/DLP ===&lt;br /&gt;
The two most accessible 3D-printing technologies that can be used to create molecular models are:&lt;br /&gt;
* &#039;&#039;&#039;FDM (Fused Deposition Modeling)&#039;&#039;&#039;&lt;br /&gt;
This method extrudes a heated thermoplastic filament (such as PLA, PETG or TPU) through a fine nozzle, depositing successive layers that form the model. FDM printers have the advantages of low cost, easy maintenance, wide availability, and being capable of printing large and colorful molecular models. This technology has a few limitations, such as: visible layer lines, lower surface resolution, and less suited for very small or intricate molecular details.&lt;br /&gt;
* &#039;&#039;&#039;SLA/DLP (Resin Printing)&#039;&#039;&#039;&lt;br /&gt;
This technique uses liquid photopolymer resin, cured layer by layer with ultraviolet light. SLA/DLP printers have the advantages of a very high resolution, smooth surfaces and are ideal for compact and detailed models (e.g., small proteins rendered as surface, ligands, or symmetric assemblies). This technology has its own limitations, such as higher material cost, post-processing requirements (washing and UV-curing), and the need for careful handling of resin.&lt;br /&gt;
&lt;br /&gt;
When choosing between FDM and SLA printers, model size and resolution are the key criteria: &#039;&#039;&#039;FDM&#039;&#039;&#039; is preferred for &#039;&#039;large, educational display models&#039;&#039;; &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; is optimal for &#039;&#039;small, precise structures&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
While FDM and SLA/DLP are the most widely used technologies in educational and research contexts due to their accessibility, other additive manufacturing methods also exist —such as &#039;&#039;Selective Laser Sintering&#039;&#039; (SLS), &#039;&#039;PolyJet&#039;&#039;, and &#039;&#039;Binder Jetting&#039;&#039;— each employing different materials and curing mechanisms. These industrial-grade techniques can produce highly detailed or multi-material parts but are generally more expensive and less accessible for classroom use. For an overview of major 3D-printing technologies, see [https://all3dp.com/1/types-of-3d-printers-3d-printing-technology/ All3DP: Complete Overview of the Types of 3D Printers]&lt;br /&gt;
&lt;br /&gt;
=== Single- vs. Multi-Material Printers ===&lt;br /&gt;
Most entry-level desktop 3D printers use a single filament or resin, producing models in one color or material. However, multi-material systems (such as [https://eu.store.bambulab.com/products/ams-multicolor-printing?from=home_web_top_navigation Bambu Lab AMS] and its variants or [https://www.prusa3d.com/category/original-prusa-mmu3/ Prusa MMU3]) can simultaneously print multiple filaments, enabling color-coded domains, subunits, or ligands directly in one print. For complex color information, users can also apply post-print color coding (painting or labeling) or print separate parts and assemble them manually.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A large FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A multi-material FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Small resin-printed models&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:GABAA_receptor.png|320px|center|thumb| GABAA receptor, [[6x3x]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Bacterial_Ribosome_multimaterial_FDM.png|348px|center|thumb| Bacterial 70S ribosome, [[4v5d]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Dna_insuline_sla.png|252px|center|thumb|DNA (left) and insulin (right) models, [[4bna]] and [[4ins]], scale at the bottom in cm]]&lt;br /&gt;
|-&lt;br /&gt;
|Trace Model of the GABAA receptor printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com] &lt;br /&gt;
|Surface model of the Bacterial 70S ribosome printed on a multi-material capable printer (BambuLab X1C AMS). Blue and violet are ribosomal proteins, orange and yellow are rRNAs, and black is tRNA. Printable files available on [https://www.printables.com/model/1430877-bacterial-70s-ribosome Printables.com]&lt;br /&gt;
|Balls and sticks and cartoon models of DNA (right) and insulin (left)&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== File Formats Used in 3D Printing ===&lt;br /&gt;
Proteopedia supports two export formats for generating printable molecular models:&lt;br /&gt;
*&#039;&#039;&#039;.STL&#039;&#039;&#039; (Stereolithography): the most common and universally compatible format; encodes only surface geometry, without color or texture information.&lt;br /&gt;
*&#039;&#039;&#039;.OBJ&#039;&#039;&#039; (Wavefront Object) with an associated &#039;&#039;&#039;.MTL&#039;&#039;&#039; (Material Template Library) files: includes both geometry and optional color/texture data; useful for color prints.&lt;br /&gt;
&lt;br /&gt;
Another widely adopted file format used in 3D printing is the &#039;&#039;&#039;.3MF&#039;&#039;&#039; (3D Manufacturing Format): a modern open standard that stores geometry, color, and multi-material metadata in a single file—recommended for advanced printers. For a more extensive pros and cons of different 3D printing file formats please see [https://all3dp.com/2/3d-file-format-3d-model-types/ The Main 3D Printing File Formats on all3dp]. &lt;br /&gt;
&lt;br /&gt;
STL is ideal for single-color models and maximum compatibility, while OBJ/MTL is recommended for multi-material workflows. 3MF files will be used in this tutorial to save the model and printing settings. &lt;br /&gt;
&lt;br /&gt;
Support in Proteopedia for these formats is based on the export capabilities of Jmol/JSmol; for details, see [http://wiki.jmol.org/index.php/File_formats/3D_Objects#STL STL] and [http://wiki.jmol.org/index.php/File_formats/3D_Objects#OBJ OBJ]&lt;br /&gt;
&lt;br /&gt;
== Overview of the 3D printing process ==&lt;br /&gt;
3D printing enables the transformation of atomic-level structural data into tangible macromolecular models that can be explored through both sight and touch.  &lt;br /&gt;
The process generally follows several main steps, each requiring specific types of software and hardware.&lt;br /&gt;
[[Image:3D_printing_workflow_v2.png|thumb|left|400px|Overview of the 3D printing workflow for generating physical molecular models.]]&lt;br /&gt;
	&lt;br /&gt;
=== Preparing the structure and generating a printable File ===&lt;br /&gt;
:The first stage involves creating a printable three-dimensional representation of the molecule. Some molecular-graphics programs such as [https://www.pymol.org/ PyMOL], [https://www.rbvi.ucsf.edu/chimerax/ UCSF ChimeraX], [https://molstar.org/Mol*], or [https://jmol.sourceforge.net/ Jmol] can be used not only to visualize a structure (from the Protein Data Bank or other sources), but also to export the resulting geometry in a .STL or .OBJ format. However, the default visualization styles of these programs are &#039;&#039;&#039;&#039;&#039;not directly suitable for 3D printing&#039;&#039;&#039;&#039;&#039;. Therefore, when preparing a model for fabrication, it is important to:&lt;br /&gt;
:* &#039;&#039;&#039;Select an appropriate molecular representation&#039;&#039;&#039; (e.g., surface, cartoon, sticks, spheres) depending on the pedagogical or structural feature you wish to highlight.  &lt;br /&gt;
:* &#039;&#039;&#039;Add struts or connectors&#039;&#039;&#039; to increase the mechanical stability of the model, especially for large complexes or long helices.  &lt;br /&gt;
:* &#039;&#039;&#039;Remove specific struts or pseudobonds&#039;&#039;&#039; when individual components — ligands, subunits, or cofactors — need to remain detachable.  &lt;br /&gt;
:* &#039;&#039;&#039;Adjust thickness&#039;&#039;&#039; of atoms, bonds, helices, and sheets to ensure adequate rigidity and printability (features thinner than the printer’s nozzle diameter or resin resolution may break).  &lt;br /&gt;
:* &#039;&#039;&#039;Apply meaningful coloring&#039;&#039;&#039; when preparing multi-material prints, for instance, to distinguish domains, chains, ligands or atoms.&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene that automates the process and enables users to effortlessly generate 3D-printable molecular models - more on that in the corresponding section [[#Generating printable files on Proteopedia|Generating printable files on Proteopedia]] within this page. For advanced users wanting to do this manually, we highly recommend two guides: &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot; /&amp;gt; and &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
=== Slicing the Model ===&lt;br /&gt;
Before printing, the STL file must be processed by a &#039;&#039;&#039;slicer&#039;&#039;&#039; — specialized software that converts 3D geometry into a series of horizontal layers. The slicer also generates &#039;&#039;&#039;G-code&#039;&#039;&#039;, the set of instructions that control the printer. These commands are printer-specific and include parameters such as extrusion speed, layer thickness, temperature, and movement. Together, they are usually stored as a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;.  &lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an FDM printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;number of perimeters&#039;&#039;&#039;, which affects mechanical strength and print time;&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines resolution and print duration;&lt;br /&gt;
:* &#039;&#039;&#039;infill density&#039;&#039;&#039;, which determines internal strength and affects print time;&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, temporary structures that hold overhanging regions;&lt;br /&gt;
:* &#039;&#039;&#039;print orientation&#039;&#039;&#039;, which influences surface quality, mechanical strength, and the amount of supports required.&lt;br /&gt;
:All these parameters make up a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. In this step, users must also select the material-specific parameters, or apply a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. More details on these profiles are provided later on this page.&lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines vertical resolution and print time; thinner layers produce smoother surfaces but significantly increase printing duration.&lt;br /&gt;
:* &#039;&#039;&#039;exposure time&#039;&#039;&#039;, which controls how long each layer is cured by UV light; optimal exposure ensures proper adhesion between layers without over-curing fine details.&lt;br /&gt;
:* &#039;&#039;&#039;bottom-layer exposure and count&#039;&#039;&#039;, which influence model adhesion to the build platform — longer exposures and additional base layers improve stability during printing.&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, which anchor the model to the build plate and prevent deformation during peeling; proper placement reduces surface marks and print failures.&lt;br /&gt;
:* &#039;&#039;&#039;model orientation&#039;&#039;&#039;, which affects surface quality, support contact area, and resin drainage; angling the model (typically 30–45°) minimizes suction forces and improves print reliability.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for FDM printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for resin printing&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:Insuline_sliced_prusa.gif|386px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|[[Image:Insuline_Sliced_SLA.gif|372px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|-&lt;br /&gt;
|Cartoon model of insulin sliced in PrusaSlicer and ready to be printed on FDM printers. The arrow shows the trajectory of the print head on a single slice or layer. Orange is the model, green are the supports. &lt;br /&gt;
|Cartoon model of insulin sliced in Elegoo SatelLite and ready to be printed on FDM printer.On the left, with blue is the model, with gray are the supports. On the right is the image on the UV screen. &lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== 3D Printing the Model ===&lt;br /&gt;
:The prepared G-code is then transferred to the 3D printer, either via an SD card, USB flash drive, or Wi-Fi connection. During printing, close observation of the first few layers is essential to ensure good adhesion to the build plate and a successful print. Total printing time depends on model size, selected layer height, and printer speed. &#039;&#039;Small peptide&#039;&#039; models may print in &#039;&#039;&#039;less than an hour&#039;&#039;&#039;, whereas l&#039;&#039;arge multimeric assemblies&#039;&#039; can require &#039;&#039;&#039;several hours or days&#039;&#039;&#039;. &#039;&#039;Multi-color&#039;&#039; or &#039;&#039;multi-material&#039;&#039; prints generally take &#039;&#039;&#039;longer&#039;&#039;&#039;, while &#039;&#039;SLA/DLP&#039;&#039; printers are generally &#039;&#039;&#039;faster&#039;&#039;&#039; due to their simultaneous layer exposure.&lt;br /&gt;
=== Post-Processing ===&lt;br /&gt;
:After printing, the model undergoes post-processing, which varies depending on the printing technology used:&lt;br /&gt;
:* For &#039;&#039;&#039;FDM prints&#039;&#039;&#039;, supports are removed mechanically, and surfaces can be smoothed by light sanding or polishing.&lt;br /&gt;
:* For &#039;&#039;&#039;resin prints&#039;&#039;&#039;, supports are removed mechanically, parts are washed in isopropanol to remove uncured resin and then exposed to UV light for final curing.&lt;br /&gt;
:Models printed in multiple parts can be assembled using cyanoacrylate or epoxy adhesive. Optional finishing steps (painting, labeling) can improve contrast between subunits or highlight functional regions.&lt;br /&gt;
&lt;br /&gt;
==Generating printable files on Proteopedia==&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene, enabling logged-in users to effortlessly generate 3D-printable molecular models directly from its pages. The tool is powered by [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;], a script that analyzes the structural data and automatically scales the model’s geometry to match the printable volume of a medium-size desktop 3D printer (e.g., Ender-3, 210×210×210 mm). During this process, the tool evaluates the molecular bounding box, atom radii, and bond lengths, then proportionally adjusts all dimensions to achieve a realistic and mechanically robust print scale — preserving scientific accuracy while ensuring manufacturability. For advanced users, [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;] may also be used in conjunction with the [https://jmol.sourceforge.net/ &#039;&#039;&#039;Jmol&#039;&#039;&#039;] program, providing full access to its scripting capabilities and advanced export features.&lt;br /&gt;
==Step-by-step guide for automatic generation of printable files on Proteopedia==&lt;br /&gt;
=== Open a structure and access the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool ===&lt;br /&gt;
Log in with your Proteopedia Username and password. Navigate to any Proteopedia page (for example, [[Introduction_to_protein_structure]]). The corresponding 3D structure will load in the viewer on the right.  &lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_button_in_Proteopedia.png|thumb|left|400px|The &#039;&#039;&#039;Print3D&#039;&#039;&#039; button on a Proteopedia page]]&lt;br /&gt;
&lt;br /&gt;
At the bottom of the structure display window, locate and click the &#039;&#039;&#039;Print3D&#039;&#039;&#039; button. The tool will launch and begin analyzing the current molecular structure.  &lt;br /&gt;
This process may take some time to complete, depending on the size of the structure.  &lt;br /&gt;
Please wait until the message &#039;&#039;&#039;Analyzing structure...&#039;&#039;&#039; disappears and the next page is displayed — this marks the start of the two-step printing workflow.&lt;br /&gt;
=== Select a molecular representation and a printing scale ===&lt;br /&gt;
In this new page, some user input is required. Each option includes a short explanation; the key steps are outlined below, but feel free to explore and adopt the settings that best fit your use case.&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step1.png|thumb|left|400px|Selecting molecular representation and printing scale]]&lt;br /&gt;
&lt;br /&gt;
(1) &#039;&#039;&#039;Choose a molecular representation&#039;&#039;&#039; from the &#039;&#039;&#039;Scheme&#039;&#039;&#039; list, based on your goal:&lt;br /&gt;
* &#039;&#039;&#039;Backbone&#039;&#039;&#039;, &#039;&#039;&#039;Trace&#039;&#039;&#039;, or &#039;&#039;&#039;Ribbon&#039;&#039;&#039; — to emphasize secondary structure (effective for teaching protein folds).&lt;br /&gt;
* &#039;&#039;&#039;Surface&#039;&#039;&#039; — to highlight molecular topology and binding sites.&lt;br /&gt;
* &#039;&#039;&#039;Ball &amp;amp; Stick&#039;&#039;&#039; — atom-level detail for ligands or small molecules; usually impractical for large proteins or complexes.&lt;br /&gt;
* &#039;&#039;&#039;Proteopedia Scene&#039;&#039;&#039; — attempts to render the current page’s scene directly; may not work for all scenes. This is not fully implemented and only available for a few users.&lt;br /&gt;
&#039;&#039;Note:&#039;&#039; Some representations may be unavailable for a given structure because they are not printable in a reliable way.&lt;br /&gt;
&lt;br /&gt;
(2) In the &#039;&#039;&#039;Printer&#039;&#039;&#039; section, select whether you want a &#039;&#039;&#039;single-color&#039;&#039;&#039; or a &#039;&#039;&#039;multi-color&#039;&#039;&#039; print.&lt;br /&gt;
&lt;br /&gt;
(3) In the &#039;&#039;&#039;Printer scale&#039;&#039;&#039; section, set the desired size of the printed model. The tool constrains safe sizes based on the chosen representation and displays the physical dimensions (mm). &#039;&#039;&#039;Important! Please note the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;printer scale value in %&amp;lt;/span&amp;gt; as it is going to be required downstream in the next section of this workflow, [[#Printing files from Proteopedia|Printing files from Proteopedia]]&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
(4) When ready, click the green &#039;&#039;&#039;Make printer files&#039;&#039;&#039; button. Please wait patiently until the  &#039;&#039;Generating files for 3D printing of...&#039;&#039; message disappears and the final step is displayed.&lt;br /&gt;
&lt;br /&gt;
===Download the .STL or .OBJ files===&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step2.png|thumb|left|400px|Final step in generating printable files]]&lt;br /&gt;
&lt;br /&gt;
In this final page, a 3D preview of the generated model is displayed.&lt;br /&gt;
You can use the mouse to rotate, zoom, and inspect the model from different angles. If the result meets your needs, click the green (A) &#039;&#039;&#039;Download files&#039;&#039;&#039; button and save the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive containing the &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; files on your computer. If your model needs further improvements, hit the green (B) &#039;&#039;&#039;Same structure&#039;&#039;&#039; button to return to the previous screen and adjust your settings.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{clear}}&lt;br /&gt;
== Printing files from Proteopedia ==&lt;br /&gt;
Unzipping the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive will produce the exported &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file, along with an optional &#039;&#039;&#039;.MTL&#039;&#039;&#039; material file. &lt;br /&gt;
=== Using 3D printing services ===&lt;br /&gt;
If you do not have a 3D printer, you can still obtain physical models by using locally available 3D-printing services. Just search on [https://www.google.com/maps Google Maps] with the term  &#039;&#039;&#039;3D printing&#039;&#039;&#039; in your area. Here is short list of well-known 3D Printing service providers that may also ship worldwide: &lt;br /&gt;
&lt;br /&gt;
* [https://www.shapeways.com/ &#039;&#039;&#039;Shapeways&#039;&#039;&#039;] — global service offering a wide range of materials and colors. Educational discounts are available through their academic program.&lt;br /&gt;
* [https://www.sculpteo.com/en/ &#039;&#039;&#039;Sculpteo&#039;&#039;&#039;] — Europe-based provider offering fast turnaround and many printing technologies, including resin and polymer options.&lt;br /&gt;
* [https://www.xometry.com/capabilities/3d-printing-service &#039;&#039;&#039;Xometry&#039;&#039;&#039;] — large international network providing access to industrial-grade printing methods such as FDM, SLA, SLS, and DMLS.&lt;br /&gt;
* [https://craftcloud3d.com/ &#039;&#039;&#039;Craftcloud&#039;&#039;&#039;] — an aggregator that compares multiple providers and finds the best price and lead time for your uploaded model.&lt;br /&gt;
&lt;br /&gt;
When contacting a printing service, provide the exported files together with the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value in %&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ([[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). It is also advisable to share the link to this Proteopedia page so that the operator understands the peculiarities of printing molecular models. &lt;br /&gt;
&lt;br /&gt;
=== Using a desktop 3D printer ===&lt;br /&gt;
&lt;br /&gt;
Before importing the .STL or .OBJ file into your slicer software, it is recommended to inspect and, if necessary, repair the model to ensure printability. Common issues include non-manifold geometry, intersecting faces, and missing surfaces.  The example below demonstrates how to use [https://www.blender.org/ &#039;&#039;&#039;Blender&#039;&#039;&#039;] together with its [https://extensions.blender.org/add-ons/print3d-toolbox/ &#039;&#039;&#039;3D Print Toolbox extension&#039;&#039;&#039;] to improve the printability of the .STL and .OBJ files generated with the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in [[Proteopedia]]. &#039;&#039;&#039;Important note&#039;&#039;&#039;: The repair process is largely automated but may introduce artifacts. Carefully inspect the corrected model for any missing or distorted sections, atoms, or bonds, and determine whether these omissions affect the intended purpose of the printed model.  &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for single color or resin printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for multi-color FDM printing&lt;br /&gt;
|-&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=k6u-5JnoP-c&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=OCisrIZMIDM&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|}  &lt;br /&gt;
&lt;br /&gt;
Once the repaired &#039;&#039;&#039;.STL or .OBJ&#039;&#039;&#039; file is ready, it can be imported into your slicer software. In this step, you will prepare the file for printing by applying appropriate printer, filament, and print-settings profiles.&lt;br /&gt;
&lt;br /&gt;
*Apply the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value (%)&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ( [[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). This step ensures that the model fits your print bed and maintains structural integrity during printing. The location of the scale (%) input field varies depending on the slicer software you are using.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Orient the model on the print bed&#039;&#039;&#039; so that its largest, flattest surface rests on the bed. This minimizes the need for supports and improves adhesion. If your slicer includes an Auto Orient or Auto Arrange function, use it to optimize placement. (&#039;&#039;Hint&#039;&#039;: Bambu Studio and Orca Slicer include this feature, Ultimaker Cura has a [https://marketplace.ultimaker.com/app/cura/plugins/nallath/OrientationPlugin Auto-Orientation plugin] available, while PrusaSlicer currently does not.)&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Select the printer&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that matches your device.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Choose the material&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; corresponding to the filament type (e.g., PLA, PETG, TPU) and manufacturer you intend to use.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Adjust the printing parameters&#039;&#039;&#039; by selecting a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that defines layer height, infill, speed, and support options.&lt;br /&gt;
&lt;br /&gt;
In most cases, the default &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; and &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; provided by the slicer are sufficient. However, molecular models often include overhangs, thin connections, and complex internal geometries, which require additional supports and reinforced perimeters to ensure structural stability. For this reason, the default &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; may not yield optimal results.&lt;br /&gt;
&lt;br /&gt;
Validated printing profiles for the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool are available for several printer models. These profiles provide optimized settings that produce sturdy models, reduce material consumption, and shorten print time, ensuring consistent and reliable results. Three distinct profiles are supplied, corresponding to major molecular representations: &#039;&#039;&#039;balls and sticks&#039;&#039;&#039;, &#039;&#039;&#039;surface&#039;&#039;&#039;, and &#039;&#039;&#039;cartoon&#039;&#039;&#039;. The &#039;&#039;&#039;cartoon&#039;&#039;&#039; profile is also suitable for &#039;&#039;&#039;backbone&#039;&#039;&#039;, &#039;&#039;&#039;trace&#039;&#039;&#039;, and &#039;&#039;&#039;ribbon&#039;&#039;&#039; representations. For some printers, each profile is supplied in two variants, one using standard supports and one using tree or organic supports. In the case of multi-material printers, profiles for printing with soluble support and soluble interface are also provided.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer brand and model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Profiles provided as / Slicer&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer Type, nozle size and multi-material support&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |GitHub with profiles&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to import profiles into Slicer&lt;br /&gt;
|-&lt;br /&gt;
|Original Prusa Core One&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer ]&lt;br /&gt;
|FDM / 0.4 mm / yes, 5 colors, if MMU3 installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/Prusa%20CoreOne CoreOne]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab A1Mini&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, 4 colors if AMS Lite is installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/BambuLab%20A1Mini AiMini]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab X1 Carbon&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, up to 16 colors if multiple AMS are installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ca92e7de9c72505c1b9b09e912ad177341cabc9a/BambuLab%20X1C X1Carbon]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|- &lt;br /&gt;
|Original Prusa MK3S+&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/7a7ee68d1e19f063600f53def49a99dfefbc595d/Prusa%20MK3S%2B MK3S+]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 5 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/a653c7cc6b3dec86b90117cc450d1883cc4a80bd/Ender-5-Pro Ender5Pro]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 3 v2 with a ENDERIDEX kit&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / yes, IDEX, two filaments&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/c2c74f1261a42c160e7e3898a407f21465de2ca7/Ender3-IDEX Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Kingroon KPS3 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ea733b2d05020b99f91c92f71a039c5ba8e54108/Kingroon-KPS3-Pro Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Elegoo Mars 5 Ultra&lt;br /&gt;
|no profile needed, just be sure to add supports / [https://www.elegoo.com/pages/satellite-3d-slicer?srsltid=AfmBOopMQGHgHycHMFOZALzOIC8z7bVlSHjL_jj2ShYR4QkowYKmKzUx ELEGOO SatelLite]&lt;br /&gt;
|resin / - / no&lt;br /&gt;
|&lt;br /&gt;
|no profile needed, default settings worked, just be sure to add supports. EVO supports worked well enough.  Post-processing steps: 1)washing: at least 10 min. 2) support removal 3)curring: at least 10 min on a Elegoo Mercury Plus V3.0&lt;br /&gt;
|- &lt;br /&gt;
|} &lt;br /&gt;
&#039;&#039;&#039;Notes&#039;&#039;&#039;: &lt;br /&gt;
* These profiles were developed and validated with the support of EDUMOL3D, Project [http://cercetare.bio.uaic.ro/grupuri/bioactive/content/grants/PED2024_mm.html PN-IV-P7-7.1-PED-2024-0343] financed by the Ministry of Research, Innovation and Digitization, [https://uefiscdi.gov.ro/ UEFISCDI], Romania.&lt;br /&gt;
* The profiles are a work in progress. Please check GitHub for updates. If you have suggestions for improvements, please drop a message at marius.mihasan(@)uaic.ro&lt;br /&gt;
&lt;br /&gt;
==== &#039;&#039;&#039;Note on multi-color printing &#039;&#039;&#039; ====&lt;br /&gt;
To our knowledge, only &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039; and &#039;&#039;&#039;Orca Slicer&#039;&#039;&#039; can automatically import color information from the &#039;&#039;&#039;.MTL&#039;&#039;&#039; file associated with the printable &#039;&#039;&#039;.OBJ&#039;&#039;&#039; generated by the Proteopedia &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool.  &lt;br /&gt;
At present, &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; does not support importing &#039;&#039;&#039;.MTL&#039;&#039;&#039; files directly.&lt;br /&gt;
&lt;br /&gt;
A practical workaround for &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; users is as follows:  &lt;br /&gt;
# Open the &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file in &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039;.  &lt;br /&gt;
#Verify or adjust the color mapping as needed.  &lt;br /&gt;
#Export the model as a generic &#039;&#039;&#039;.3MF&#039;&#039;&#039; file using the menu command:  &#039;&#039;File&#039;&#039; → &#039;&#039;Export&#039;&#039; → &#039;&#039;Export Generic 3MF...&#039;&#039;  &lt;br /&gt;
#Open the exported &#039;&#039;&#039;.3MF&#039;&#039;&#039; file in &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;. The color data will now be available under the &#039;&#039;&#039;Multimaterial Painting&#039;&#039;&#039; tool.&lt;br /&gt;
&lt;br /&gt;
This workflow preserves the original coloring assigned in Proteopedia and allows successful multi-color or multi-material printing on any capable 3D printer compatible with &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Other relevant resources ==&lt;br /&gt;
[https://proteopedia.org/w/Print3D_models_gallery Print3D Models gallery] - examples of 3D printed molecular models from Proteopedia users.&lt;br /&gt;
&lt;br /&gt;
[https://3d.nih.gov/ NIH 3D Print Exchange] - an open, community-driven portal to download, share, and create bioscientific and medical 3D models, including for 3D printing.&lt;br /&gt;
  &lt;br /&gt;
[https://github.com/mariusmihasan/3DP-Jmol 3DP-Jmol] - the Jmol/JSmol behind the Print3D tool. Automatically generates 3D printable molecular models from structural data and can be easily integrated into web pages.&lt;br /&gt;
&lt;br /&gt;
[https://pdb101.rcsb.org/learn/3d-printing/pdb-structures-and-3d-printing 3D Printing on PDB101] - a quick guide on 3D printing molecular models and a small curated 3D models for education&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;If you print a model from Proteopedia, please share photos and feedback — let’s 3D print the whole Proteopedia!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4396888</id>
		<title>Print3D help</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4396888"/>
		<updated>2025-12-01T08:45:42Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== Proteopedia and 3D Printing ==&lt;br /&gt;
&lt;br /&gt;
Physical molecular models, by engaging both visual and tactile senses, provide an effective means of deepening the understanding of complex concepts in molecular biology and biochemistry. They allow students to perceive the three-dimensional organization of macromolecules, thereby enhancing comprehension of the relationship between structure and function &amp;lt;ref&amp;gt;PMID: 32590880&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 40214166&amp;lt;/ref&amp;gt;. Numerous studies have demonstrated that the use of tangible models in science education improves learning outcomes, fosters conceptual reasoning, and increases student engagement &amp;lt;ref&amp;gt;PMID: 27366318&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 26712513&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;Larsson, C., Tibell, L.A.E. Challenging Students’ Intuitions—the Influence of a Tangible Model of Virus Assembly on Students’ Conceptual Reasoning About the Process of Self-Assembly. Res Sci Educ 45, 663–690 (2015). [http://dx.doi.org/10.1007/s11165-014-9446-6 DOI: 110.1007/s11165-014-9446-6]&amp;lt;/ref&amp;gt;. The rapid development of 3D-printing technologies has made it possible to create customized and affordable molecular models  &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot;&amp;gt;PMID: 28362403&amp;lt;/ref&amp;gt; &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot;&amp;gt;PMID: 33755300&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 33384761&amp;lt;/ref&amp;gt;. &lt;br /&gt;
&lt;br /&gt;
Affordable desktop 3D printers can now be used to fabricate physical models from virtually any structure or scene on [[Proteopedia]]. This page provides an introduction to 3D printing, a step-by-step guide to generating printable files directly from [[Proteopedia]], and several tested printing profiles for common printers (e.g., Prusa Research, Bambu Lab, Creality, or Elegoo).&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== «3D Printing 101»: an introduction to 3D printing ==&lt;br /&gt;
3D printing, also known as &#039;&#039;additive manufacturing&#039;&#039;, builds physical objects layer by layer from digital designs. For more technical details please head for the excellent introductory article on [https://all3dp.com/2/what-is-3d-printing/ All3DP].  In structural biology education, 3D printing provides an affordable and accessible way to transform atomic coordinate data (e.g., from PDB, MOL or SDF files) into tangible molecular models that can be observed, handled, and discussed in class or laboratory settings.&lt;br /&gt;
&lt;br /&gt;
=== Printer Types: FDM vs. SLA/DLP ===&lt;br /&gt;
The two most accessible 3D-printing technologies that can be used to create molecular models are:&lt;br /&gt;
* &#039;&#039;&#039;FDM (Fused Deposition Modeling)&#039;&#039;&#039;&lt;br /&gt;
This method extrudes a heated thermoplastic filament (such as PLA, PETG or TPU) through a fine nozzle, depositing successive layers that form the model. FDM printers have the advantages of low cost, easy maintenance, wide availability, and being capable of printing large and colorful molecular models. This technology has a few limitations, such as: visible layer lines, lower surface resolution, and less suited for very small or intricate molecular details.&lt;br /&gt;
* &#039;&#039;&#039;SLA/DLP (Resin Printing)&#039;&#039;&#039;&lt;br /&gt;
This technique uses liquid photopolymer resin, cured layer by layer with ultraviolet light. SLA/DLP printers have the advantages of a very high resolution, smooth surfaces and are ideal for compact and detailed models (e.g., small proteins rendered as surface, ligands, or symmetric assemblies). This technology has its own limitations, such as higher material cost, post-processing requirements (washing and UV-curing), and the need for careful handling of resin.&lt;br /&gt;
&lt;br /&gt;
When choosing between FDM and SLA printers, model size and resolution are the key criteria: &#039;&#039;&#039;FDM&#039;&#039;&#039; is preferred for &#039;&#039;large, educational display models&#039;&#039;; &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; is optimal for &#039;&#039;small, precise structures&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
While FDM and SLA/DLP are the most widely used technologies in educational and research contexts due to their accessibility, other additive manufacturing methods also exist —such as &#039;&#039;Selective Laser Sintering&#039;&#039; (SLS), &#039;&#039;PolyJet&#039;&#039;, and &#039;&#039;Binder Jetting&#039;&#039;— each employing different materials and curing mechanisms. These industrial-grade techniques can produce highly detailed or multi-material parts but are generally more expensive and less accessible for classroom use. For an overview of major 3D-printing technologies, see [https://all3dp.com/1/types-of-3d-printers-3d-printing-technology/ All3DP: Complete Overview of the Types of 3D Printers]&lt;br /&gt;
&lt;br /&gt;
=== Single- vs. Multi-Material Printers ===&lt;br /&gt;
Most entry-level desktop 3D printers use a single filament or resin, producing models in one color or material. However, multi-material systems (such as [https://eu.store.bambulab.com/products/ams-multicolor-printing?from=home_web_top_navigation Bambu Lab AMS] and its variants or [https://www.prusa3d.com/category/original-prusa-mmu3/ Prusa MMU3]) can simultaneously print multiple filaments, enabling color-coded domains, subunits, or ligands directly in one print. For complex color information, users can also apply post-print color coding (painting or labeling) or print separate parts and assemble them manually.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A large FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A multi-material FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Small resin-printed models&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:GABAA_receptor.png|320px|center|thumb| GABAA receptor, [[6x3x]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Bacterial_Ribosome_multimaterial_FDM.png|348px|center|thumb| Bacterial 70S ribosome, [[4v5d]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Dna_insuline_sla.png|252px|center|thumb|DNA (left) and insulin (right) models, [[4bna]] and [[4ins]], scale at the bottom in cm]]&lt;br /&gt;
|-&lt;br /&gt;
|Trace Model of the GABAA receptor printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com] &lt;br /&gt;
|Surface model of the Bacterial 70S ribosome printed on a multi-material capable printer (BambuLab X1C AMS). Blue and violet are ribosomal proteins, orange and yellow are rRNAs, and black is tRNA. Printable files available on [https://www.printables.com/model/1430877-bacterial-70s-ribosome Printables.com]&lt;br /&gt;
|Balls and sticks and cartoon models of DNA (right) and insulin (left)&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== File Formats Used in 3D Printing ===&lt;br /&gt;
Proteopedia supports two export formats for generating printable molecular models:&lt;br /&gt;
*&#039;&#039;&#039;.STL&#039;&#039;&#039; (Stereolithography): the most common and universally compatible format; encodes only surface geometry, without color or texture information.&lt;br /&gt;
*&#039;&#039;&#039;.OBJ&#039;&#039;&#039; (Wavefront Object) with an associated &#039;&#039;&#039;.MTL&#039;&#039;&#039; (Material Template Library) files: includes both geometry and optional color/texture data; useful for color prints.&lt;br /&gt;
&lt;br /&gt;
Another widely adopted file format used in 3D printing is the &#039;&#039;&#039;.3MF&#039;&#039;&#039; (3D Manufacturing Format): a modern open standard that stores geometry, color, and multi-material metadata in a single file—recommended for advanced printers. For a more extensive pros and cons of different 3D printing file formats please see [https://all3dp.com/2/3d-file-format-3d-model-types/ The Main 3D Printing File Formats on all3dp]. &lt;br /&gt;
&lt;br /&gt;
STL is ideal for single-color models and maximum compatibility, while OBJ/MTL is recommended for multi-material workflows. 3MF files will be used in this tutorial to save the model and printing settings. &lt;br /&gt;
&lt;br /&gt;
Support in Proteopedia for these formats is based on the export capabilities of Jmol/JSmol; for details, see [http://wiki.jmol.org/index.php/File_formats/3D_Objects#STL STL] and [http://wiki.jmol.org/index.php/File_formats/3D_Objects#OBJ OBJ]&lt;br /&gt;
&lt;br /&gt;
== Overview of the 3D printing process ==&lt;br /&gt;
3D printing enables the transformation of atomic-level structural data into tangible macromolecular models that can be explored through both sight and touch.  &lt;br /&gt;
The process generally follows several main steps, each requiring specific types of software and hardware.&lt;br /&gt;
[[Image:3D_printing_workflow_v2.png|thumb|left|400px|Overview of the 3D printing workflow for generating physical molecular models.]]&lt;br /&gt;
	&lt;br /&gt;
=== Preparing the structure and generating a printable File ===&lt;br /&gt;
:The first stage involves creating a printable three-dimensional representation of the molecule. Some molecular-graphics programs such as [https://www.pymol.org/ PyMOL], [https://www.rbvi.ucsf.edu/chimerax/ UCSF ChimeraX], [https://molstar.org/Mol*], or [https://jmol.sourceforge.net/ Jmol] can be used not only to visualize a structure (from the Protein Data Bank or other sources), but also to export the resulting geometry in a .STL or .OBJ format. However, the default visualization styles of these programs are &#039;&#039;&#039;&#039;&#039;not directly suitable for 3D printing&#039;&#039;&#039;&#039;&#039;. Therefore, when preparing a model for fabrication, it is important to:&lt;br /&gt;
:* &#039;&#039;&#039;Select an appropriate molecular representation&#039;&#039;&#039; (e.g., surface, cartoon, sticks, spheres) depending on the pedagogical or structural feature you wish to highlight.  &lt;br /&gt;
:* &#039;&#039;&#039;Add struts or connectors&#039;&#039;&#039; to increase the mechanical stability of the model, especially for large complexes or long helices.  &lt;br /&gt;
:* &#039;&#039;&#039;Remove specific struts or pseudobonds&#039;&#039;&#039; when individual components — ligands, subunits, or cofactors — need to remain detachable.  &lt;br /&gt;
:* &#039;&#039;&#039;Adjust thickness&#039;&#039;&#039; of atoms, bonds, helices, and sheets to ensure adequate rigidity and printability (features thinner than the printer’s nozzle diameter or resin resolution may break).  &lt;br /&gt;
:* &#039;&#039;&#039;Apply meaningful coloring&#039;&#039;&#039; when preparing multi-material prints, for instance, to distinguish domains, chains, ligands or atoms.&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene that automates the process and enables users to effortlessly generate 3D-printable molecular models - more on that in the corresponding section [[#Generating printable files on Proteopedia|Generating printable files on Proteopedia]] within this page. For advanced users wanting to do this manually, we highly recommend two guides: &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot; /&amp;gt; and &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
=== Slicing the Model ===&lt;br /&gt;
Before printing, the STL file must be processed by a &#039;&#039;&#039;slicer&#039;&#039;&#039; — specialized software that converts 3D geometry into a series of horizontal layers. The slicer also generates &#039;&#039;&#039;G-code&#039;&#039;&#039;, the set of instructions that control the printer. These commands are printer-specific and include parameters such as extrusion speed, layer thickness, temperature, and movement. Together, they are usually stored as a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;.  &lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an FDM printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;number of perimeters&#039;&#039;&#039;, which affects mechanical strength and print time;&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines resolution and print duration;&lt;br /&gt;
:* &#039;&#039;&#039;infill density&#039;&#039;&#039;, which determines internal strength and affects print time;&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, temporary structures that hold overhanging regions;&lt;br /&gt;
:* &#039;&#039;&#039;print orientation&#039;&#039;&#039;, which influences surface quality, mechanical strength, and the amount of supports required.&lt;br /&gt;
:All these parameters make up a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. In this step, users must also select the material-specific parameters, or apply a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. More details on these profiles are provided later on this page.&lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines vertical resolution and print time; thinner layers produce smoother surfaces but significantly increase printing duration.&lt;br /&gt;
:* &#039;&#039;&#039;exposure time&#039;&#039;&#039;, which controls how long each layer is cured by UV light; optimal exposure ensures proper adhesion between layers without over-curing fine details.&lt;br /&gt;
:* &#039;&#039;&#039;bottom-layer exposure and count&#039;&#039;&#039;, which influence model adhesion to the build platform — longer exposures and additional base layers improve stability during printing.&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, which anchor the model to the build plate and prevent deformation during peeling; proper placement reduces surface marks and print failures.&lt;br /&gt;
:* &#039;&#039;&#039;model orientation&#039;&#039;&#039;, which affects surface quality, support contact area, and resin drainage; angling the model (typically 30–45°) minimizes suction forces and improves print reliability.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for FDM printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for resin printing&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:Insuline_sliced_prusa.gif|386px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|[[Image:Insuline_Sliced_SLA.gif|372px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|-&lt;br /&gt;
|Cartoon model of insulin sliced in PrusaSlicer and ready to be printed on FDM printers. The arrow shows the trajectory of the print head on a single slice or layer. Orange is the model, green are the supports. &lt;br /&gt;
|Cartoon model of insulin sliced in Elegoo SatelLite and ready to be printed on FDM printer.On the left, with blue is the model, with gray are the supports. On the right is the image on the UV screen. &lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== 3D Printing the Model ===&lt;br /&gt;
:The prepared G-code is then transferred to the 3D printer, either via an SD card, USB flash drive, or Wi-Fi connection. During printing, close observation of the first few layers is essential to ensure good adhesion to the build plate and a successful print. Total printing time depends on model size, selected layer height, and printer speed. &#039;&#039;Small peptide&#039;&#039; models may print in &#039;&#039;&#039;less than an hour&#039;&#039;&#039;, whereas l&#039;&#039;arge multimeric assemblies&#039;&#039; can require &#039;&#039;&#039;several hours or days&#039;&#039;&#039;. &#039;&#039;Multi-color&#039;&#039; or &#039;&#039;multi-material&#039;&#039; prints generally take &#039;&#039;&#039;longer&#039;&#039;&#039;, while &#039;&#039;SLA/DLP&#039;&#039; printers are generally &#039;&#039;&#039;faster&#039;&#039;&#039; due to their simultaneous layer exposure.&lt;br /&gt;
=== Post-Processing ===&lt;br /&gt;
:After printing, the model undergoes post-processing, which varies depending on the printing technology used:&lt;br /&gt;
:* For &#039;&#039;&#039;FDM prints&#039;&#039;&#039;, supports are removed mechanically, and surfaces can be smoothed by light sanding or polishing.&lt;br /&gt;
:* For &#039;&#039;&#039;resin prints&#039;&#039;&#039;, supports are removed mechanically, parts are washed in isopropanol to remove uncured resin and then exposed to UV light for final curing.&lt;br /&gt;
:Models printed in multiple parts can be assembled using cyanoacrylate or epoxy adhesive. Optional finishing steps (painting, labeling) can improve contrast between subunits or highlight functional regions.&lt;br /&gt;
&lt;br /&gt;
==Generating printable files on Proteopedia==&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene, enabling logged-in users to effortlessly generate 3D-printable molecular models directly from its pages. The tool is powered by [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;], a script that analyzes the structural data and automatically scales the model’s geometry to match the printable volume of a medium-size desktop 3D printer (e.g., Ender-3, 210×210×210 mm). During this process, the tool evaluates the molecular bounding box, atom radii, and bond lengths, then proportionally adjusts all dimensions to achieve a realistic and mechanically robust print scale — preserving scientific accuracy while ensuring manufacturability. For advanced users, [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;] may also be used in conjunction with the [https://jmol.sourceforge.net/ &#039;&#039;&#039;Jmol&#039;&#039;&#039;] program, providing full access to its scripting capabilities and advanced export features.&lt;br /&gt;
==Step-by-step guide for automatic generation of printable files on Proteopedia==&lt;br /&gt;
=== Open a structure and access the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool ===&lt;br /&gt;
Log in with your Proteopedia Username and password. Navigate to any Proteopedia page (for example, [[Introduction_to_protein_structure]]). The corresponding 3D structure will load in the viewer on the right.  &lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_button_in_Proteopedia.png|thumb|left|400px|The &#039;&#039;&#039;Print3D&#039;&#039;&#039; button on a Proteopedia page]]&lt;br /&gt;
&lt;br /&gt;
At the bottom of the structure display window, locate and click the &#039;&#039;&#039;Print3D&#039;&#039;&#039; button. The tool will launch and begin analyzing the current molecular structure.  &lt;br /&gt;
This process may take some time to complete, depending on the size of the structure.  &lt;br /&gt;
Please wait until the message &#039;&#039;&#039;Analyzing structure...&#039;&#039;&#039; disappears and the next page is displayed — this marks the start of the two-step printing workflow.&lt;br /&gt;
=== Select a molecular representation and a printing scale ===&lt;br /&gt;
In this new page, some user input is required. Each option includes a short explanation; the key steps are outlined below, but feel free to explore and adopt the settings that best fit your use case.&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step1.png|thumb|left|400px|Selecting molecular representation and printing scale]]&lt;br /&gt;
&lt;br /&gt;
(1) &#039;&#039;&#039;Choose a molecular representation&#039;&#039;&#039; from the &#039;&#039;&#039;Scheme&#039;&#039;&#039; list, based on your goal:&lt;br /&gt;
* &#039;&#039;&#039;Backbone&#039;&#039;&#039;, &#039;&#039;&#039;Trace&#039;&#039;&#039;, or &#039;&#039;&#039;Ribbon&#039;&#039;&#039; — to emphasize secondary structure (effective for teaching protein folds).&lt;br /&gt;
* &#039;&#039;&#039;Surface&#039;&#039;&#039; — to highlight molecular topology and binding sites.&lt;br /&gt;
* &#039;&#039;&#039;Ball &amp;amp; Stick&#039;&#039;&#039; — atom-level detail for ligands or small molecules; usually impractical for large proteins or complexes.&lt;br /&gt;
* &#039;&#039;&#039;Proteopedia Scene&#039;&#039;&#039; — attempts to render the current page’s scene directly; may not work for all scenes. This is not fully implemented and only available for a few users.&lt;br /&gt;
&#039;&#039;Note:&#039;&#039; Some representations may be unavailable for a given structure because they are not printable in a reliable way.&lt;br /&gt;
&lt;br /&gt;
(2) In the &#039;&#039;&#039;Printer&#039;&#039;&#039; section, select whether you want a &#039;&#039;&#039;single-color&#039;&#039;&#039; or a &#039;&#039;&#039;multi-color&#039;&#039;&#039; print.&lt;br /&gt;
&lt;br /&gt;
(3) In the &#039;&#039;&#039;Printer scale&#039;&#039;&#039; section, set the desired size of the printed model. The tool constrains safe sizes based on the chosen representation and displays the physical dimensions (mm). &#039;&#039;&#039;Important! Please note the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;printer scale value in %&amp;lt;/span&amp;gt; as it is going to be required downstream in the next section of this workflow, [[#Printing files from Proteopedia|Printing files from Proteopedia]]&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
(4) When ready, click the green &#039;&#039;&#039;Make printer files&#039;&#039;&#039; button. Please wait patiently until the  &#039;&#039;Generating files for 3D printing of...&#039;&#039; message disappears and the final step is displayed.&lt;br /&gt;
&lt;br /&gt;
===Download the .STL or .OBJ files===&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step2.png|thumb|left|400px|Final step in generating printable files]]&lt;br /&gt;
&lt;br /&gt;
In this final page, a 3D preview of the generated model is displayed.&lt;br /&gt;
You can use the mouse to rotate, zoom, and inspect the model from different angles. If the result meets your needs, click the green (A) &#039;&#039;&#039;Download files&#039;&#039;&#039; button and save the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive containing the &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; files on your computer. If your model needs further improvements, hit the green (B) &#039;&#039;&#039;Same structure&#039;&#039;&#039; button to return to the previous screen and adjust your settings.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{clear}}&lt;br /&gt;
== Printing files from Proteopedia ==&lt;br /&gt;
Unzipping the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive will produce the exported &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file, along with an optional &#039;&#039;&#039;.MTL&#039;&#039;&#039; material file. &lt;br /&gt;
=== Using 3D printing services ===&lt;br /&gt;
If you do not have a 3D printer, you can still obtain physical models by using locally available 3D-printing services. Just search on [https://www.google.com/maps Google Maps] with the term  &#039;&#039;&#039;3D printing&#039;&#039;&#039; in your area. Here is short list of well-known 3D Printing service providers that may also ship worldwide: &lt;br /&gt;
&lt;br /&gt;
* [https://www.shapeways.com/ &#039;&#039;&#039;Shapeways&#039;&#039;&#039;] — global service offering a wide range of materials and colors. Educational discounts are available through their academic program.&lt;br /&gt;
* [https://www.sculpteo.com/en/ &#039;&#039;&#039;Sculpteo&#039;&#039;&#039;] — Europe-based provider offering fast turnaround and many printing technologies, including resin and polymer options.&lt;br /&gt;
* [https://www.xometry.com/capabilities/3d-printing-service &#039;&#039;&#039;Xometry&#039;&#039;&#039;] — large international network providing access to industrial-grade printing methods such as FDM, SLA, SLS, and DMLS.&lt;br /&gt;
* [https://craftcloud3d.com/ &#039;&#039;&#039;Craftcloud&#039;&#039;&#039;] — an aggregator that compares multiple providers and finds the best price and lead time for your uploaded model.&lt;br /&gt;
&lt;br /&gt;
When contacting a printing service, provide the exported files together with the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value in %&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ([[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). It is also advisable to share the link to this Proteopedia page so that the operator understands the peculiarities of printing molecular models. &lt;br /&gt;
&lt;br /&gt;
=== Using a desktop 3D printer ===&lt;br /&gt;
&lt;br /&gt;
Before importing the .STL or .OBJ file into your slicer software, it is recommended to inspect and, if necessary, repair the model to ensure printability. Common issues include non-manifold geometry, intersecting faces, and missing surfaces.  The example below demonstrates how to use [https://www.blender.org/ &#039;&#039;&#039;Blender&#039;&#039;&#039;] together with its [https://extensions.blender.org/add-ons/print3d-toolbox/ &#039;&#039;&#039;3D Print Toolbox extension&#039;&#039;&#039;] to improve the printability of the .STL and .OBJ files generated with the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in [[Proteopedia]]. &#039;&#039;&#039;Important note&#039;&#039;&#039;: The repair process is largely automated but may introduce artifacts. Carefully inspect the corrected model for any missing or distorted sections, atoms, or bonds, and determine whether these omissions affect the intended purpose of the printed model.  &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for single color or resin printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for multi-color FDM printing&lt;br /&gt;
|-&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=k6u-5JnoP-c&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=OCisrIZMIDM&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|}  &lt;br /&gt;
&lt;br /&gt;
Once the repaired &#039;&#039;&#039;.STL or .OBJ&#039;&#039;&#039; file is ready, it can be imported into your slicer software. In this step, you will prepare the file for printing by applying appropriate printer, filament, and print-settings profiles.&lt;br /&gt;
&lt;br /&gt;
*Apply the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value (%)&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ( [[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). This step ensures that the model fits your print bed and maintains structural integrity during printing. The location of the scale (%) input field varies depending on the slicer software you are using.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Orient the model on the print bed&#039;&#039;&#039; so that its largest, flattest surface rests on the bed. This minimizes the need for supports and improves adhesion. If your slicer includes an Auto Orient or Auto Arrange function, use it to optimize placement. (&#039;&#039;Hint&#039;&#039;: Bambu Studio and Orca Slicer include this feature, Ultimaker Cura has a [https://marketplace.ultimaker.com/app/cura/plugins/nallath/OrientationPlugin Auto-Orientation plugin] available, while PrusaSlicer currently does not.)&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Select the printer&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that matches your device.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Choose the material&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; corresponding to the filament type (e.g., PLA, PETG, TPU) and manufacturer you intend to use.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Adjust the printing parameters&#039;&#039;&#039; by selecting a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that defines layer height, infill, speed, and support options.&lt;br /&gt;
&lt;br /&gt;
In most cases, the default &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; and &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; provided by the slicer are sufficient. However, molecular models often include overhangs, thin connections, and complex internal geometries, which require additional supports and reinforced perimeters to ensure structural stability. For this reason, the default &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; may not yield optimal results.&lt;br /&gt;
&lt;br /&gt;
Validated printing profiles for the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool are available for several printer models. These profiles provide optimized settings that produce sturdy models, reduce material consumption, and shorten print time, ensuring consistent and reliable results. Three distinct profiles are supplied, corresponding to major molecular representations: &#039;&#039;&#039;balls and sticks&#039;&#039;&#039;, &#039;&#039;&#039;surface&#039;&#039;&#039;, and &#039;&#039;&#039;cartoon&#039;&#039;&#039;. The &#039;&#039;&#039;cartoon&#039;&#039;&#039; profile is also suitable for &#039;&#039;&#039;backbone&#039;&#039;&#039;, &#039;&#039;&#039;trace&#039;&#039;&#039;, and &#039;&#039;&#039;ribbon&#039;&#039;&#039; representations. For some printers, each profile is supplied in two variants, one using standard supports and one using tree or organic supports. In the case of multi-material printers, profiles for printing with soluble support and soluble interface are also provided.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer brand and model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Profiles provided as / Slicer&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer Type, nozle size and multi-material support&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |GitHub with profiles&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to import profiles into Slicer&lt;br /&gt;
|-&lt;br /&gt;
|Original Prusa Core One&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer ]&lt;br /&gt;
|FDM / 0.4 mm / yes, 5 colors, if MMU3 installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/Prusa%20CoreOne CoreOne]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab A1Mini&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, 4 colors if AMS Lite is installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/BambuLab%20A1Mini AiMini]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab X1 Carbon&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, up to 16 colors if multiple AMS are installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ca92e7de9c72505c1b9b09e912ad177341cabc9a/BambuLab%20X1C X1Carbon]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|- &lt;br /&gt;
|Original Prusa MK3S+&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/7a7ee68d1e19f063600f53def49a99dfefbc595d/Prusa%20MK3S%2B MK3S+]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 5 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/a653c7cc6b3dec86b90117cc450d1883cc4a80bd/Ender-5-Pro Ender5Pro]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 3 v2 with a ENDERIDEX kit&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / yes, IDEX, two filaments&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/c2c74f1261a42c160e7e3898a407f21465de2ca7/Ender3-IDEX Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Kingroon KPS3 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ea733b2d05020b99f91c92f71a039c5ba8e54108/Kingroon-KPS3-Pro Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Elegoo Mars 5 Ultra&lt;br /&gt;
|no profile needed, just be sure to add supports / [https://www.elegoo.com/pages/satellite-3d-slicer?srsltid=AfmBOopMQGHgHycHMFOZALzOIC8z7bVlSHjL_jj2ShYR4QkowYKmKzUx ELEGOO SatelLite]&lt;br /&gt;
|resin / - / no&lt;br /&gt;
|&lt;br /&gt;
|no profile needed, default settings worked, just be sure to add supports. EVO supports worked well enough.  Post-processing steps: 1)washing: at least 10 min. 2) support removal 3)curring: at least 10 min on a Elegoo Mercury Plus V3.0&lt;br /&gt;
|- &lt;br /&gt;
|} &lt;br /&gt;
&#039;&#039;&#039;Notes&#039;&#039;&#039;: &lt;br /&gt;
* These profiles were developed and validated with the support of EDUMOL3D, Project [http://cercetare.bio.uaic.ro/grupuri/bioactive/content/grants/PED2024_mm.html PN-IV-P7-7.1-PED-2024-0343] financed by the Ministry of Research, Innovation and Digitization, [https://uefiscdi.gov.ro/ UEFISCDI], Romania.&lt;br /&gt;
* The profiles are a work in progress. Please check GitHub for updates. If you have suggestions for improvements, please drop a message at marius.mihasan(@)uaic.ro&lt;br /&gt;
&lt;br /&gt;
==== &#039;&#039;&#039;Note on multi-color printing &#039;&#039;&#039; ====&lt;br /&gt;
To our knowledge, only &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039; and &#039;&#039;&#039;Orca Slicer&#039;&#039;&#039; can automatically import color information from the &#039;&#039;&#039;.MTL&#039;&#039;&#039; file associated with the printable &#039;&#039;&#039;.OBJ&#039;&#039;&#039; generated by the Proteopedia &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool.  &lt;br /&gt;
At present, &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; does not support importing &#039;&#039;&#039;.MTL&#039;&#039;&#039; files directly.&lt;br /&gt;
&lt;br /&gt;
A practical workaround for &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; users is as follows:  &lt;br /&gt;
# Open the &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file in &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039;.  &lt;br /&gt;
#Verify or adjust the color mapping as needed.  &lt;br /&gt;
#Export the model as a generic &#039;&#039;&#039;.3MF&#039;&#039;&#039; file using the menu command:  &#039;&#039;File&#039;&#039; → &#039;&#039;Export&#039;&#039; → &#039;&#039;Export Generic 3MF...&#039;&#039;  &lt;br /&gt;
#Open the exported &#039;&#039;&#039;.3MF&#039;&#039;&#039; file in &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;. The color data will now be available under the &#039;&#039;&#039;Multimaterial Painting&#039;&#039;&#039; tool.&lt;br /&gt;
&lt;br /&gt;
This workflow preserves the original coloring assigned in Proteopedia and allows successful multi-color or multi-material printing on any capable 3D printer compatible with &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Other relevant resources ==&lt;br /&gt;
[https://proteopedia.org/w/Print3D_models_gallery Print3D Models gallery] - examples of 3D printed molecular models from Proteopedia users.&lt;br /&gt;
&lt;br /&gt;
[https://3d.nih.gov/ NIH 3D Print Exchange] - an open, community-driven portal to download, share, and create bioscientific and medical 3D models, including for 3D printing.&lt;br /&gt;
  &lt;br /&gt;
[https://github.com/mariusmihasan/3DP-Jmol 3DP-Jmol] - the Jmol/JSmol behind the Print3D tool. Automatically generates 3D printable molecular models from structural data and can be easily integrated into web pages.&lt;br /&gt;
&lt;br /&gt;
[https://pdb101.rcsb.org/learn/3d-printing/pdb-structures-and-3d-printing 3D Printing on PDB101] - a quick guide on 3D printing molecular models and a small curated 3D models for education&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;If you print a model from Proteopedia, please share photos and feedback — let’s 3D print the whole Proteopedia!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4396887</id>
		<title>Print3D help</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4396887"/>
		<updated>2025-12-01T08:45:04Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== Proteopedia and 3D Printing ==&lt;br /&gt;
&lt;br /&gt;
Physical molecular models, by engaging both visual and tactile senses, provide an effective means of deepening the understanding of complex concepts in molecular biology and biochemistry. They allow students to perceive the three-dimensional organization of macromolecules, thereby enhancing comprehension of the relationship between structure and function &amp;lt;ref&amp;gt;PMID: 32590880&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 40214166&amp;lt;/ref&amp;gt;. Numerous studies have demonstrated that the use of tangible models in science education improves learning outcomes, fosters conceptual reasoning, and increases student engagement &amp;lt;ref&amp;gt;PMID: 27366318&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 26712513&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;Larsson, C., Tibell, L.A.E. Challenging Students’ Intuitions—the Influence of a Tangible Model of Virus Assembly on Students’ Conceptual Reasoning About the Process of Self-Assembly. Res Sci Educ 45, 663–690 (2015). [http://dx.doi.org/10.1007/s11165-014-9446-6 DOI: 110.1007/s11165-014-9446-6]&amp;lt;/ref&amp;gt;. The rapid development of 3D-printing technologies has made it possible to create customized and affordable molecular models  &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot;&amp;gt;PMID: 28362403&amp;lt;/ref&amp;gt; &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot;&amp;gt;PMID: 33755300&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 33384761&amp;lt;/ref&amp;gt;. &lt;br /&gt;
&lt;br /&gt;
Affordable desktop 3D printers can now be used to fabricate physical models from virtually any structure or scene on [[Proteopedia]]. This page provides an introduction to 3D printing, a step-by-step guide to generating printable files directly from [[Proteopedia]], and several tested printing profiles for common printers (e.g., Prusa Research, Bambu Lab, Creality, or Elegoo).&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== «3D Printing 101»: an introduction to 3D printing ==&lt;br /&gt;
3D printing, also known as &#039;&#039;additive manufacturing&#039;&#039;, builds physical objects layer by layer from digital designs. For more technical details please head for the excellent introductory article on [https://all3dp.com/2/what-is-3d-printing/ All3DP].  In structural biology education, 3D printing provides an affordable and accessible way to transform atomic coordinate data (e.g., from PDB, MOL or SDF files) into tangible molecular models that can be observed, handled, and discussed in class or laboratory settings.&lt;br /&gt;
&lt;br /&gt;
=== Printer Types: FDM vs. SLA/DLP ===&lt;br /&gt;
The two most accessible 3D-printing technologies that can be used to create molecular models are:&lt;br /&gt;
* &#039;&#039;&#039;FDM (Fused Deposition Modeling)&#039;&#039;&#039;&lt;br /&gt;
This method extrudes a heated thermoplastic filament (such as PLA, PETG or TPU) through a fine nozzle, depositing successive layers that form the model. FDM printers have the advantages of low cost, easy maintenance, wide availability, and being capable of printing large and colorful molecular models. This technology has a few limitations, such as: visible layer lines, lower surface resolution, and less suited for very small or intricate molecular details.&lt;br /&gt;
* &#039;&#039;&#039;SLA/DLP (Resin Printing)&#039;&#039;&#039;&lt;br /&gt;
This technique uses liquid photopolymer resin, cured layer by layer with ultraviolet light. SLA/DLP printers have the advantages of a very high resolution, smooth surfaces and are ideal for compact and detailed models (e.g., small proteins rendered as surface, ligands, or symmetric assemblies). This technology has its own limitations, such as higher material cost, post-processing requirements (washing and UV-curing), and the need for careful handling of resin.&lt;br /&gt;
&lt;br /&gt;
When choosing between FDM and SLA printers, model size and resolution are the key criteria: &#039;&#039;&#039;FDM&#039;&#039;&#039; is preferred for &#039;&#039;large, educational display models&#039;&#039;; &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; is optimal for &#039;&#039;small, precise structures&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
While FDM and SLA/DLP are the most widely used technologies in educational and research contexts due to their accessibility, other additive manufacturing methods also exist —such as &#039;&#039;Selective Laser Sintering&#039;&#039; (SLS), &#039;&#039;PolyJet&#039;&#039;, and &#039;&#039;Binder Jetting&#039;&#039;— each employing different materials and curing mechanisms. These industrial-grade techniques can produce highly detailed or multi-material parts but are generally more expensive and less accessible for classroom use. For an overview of major 3D-printing technologies, see [https://all3dp.com/1/types-of-3d-printers-3d-printing-technology/ All3DP: Complete Overview of the Types of 3D Printers]&lt;br /&gt;
&lt;br /&gt;
=== Single- vs. Multi-Material Printers ===&lt;br /&gt;
Most entry-level desktop 3D printers use a single filament or resin, producing models in one color or material. However, multi-material systems (such as [https://eu.store.bambulab.com/products/ams-multicolor-printing?from=home_web_top_navigation Bambu Lab AMS] and its variants or [https://www.prusa3d.com/category/original-prusa-mmu3/ Prusa MMU3]) can simultaneously print multiple filaments, enabling color-coded domains, subunits, or ligands directly in one print. For complex color information, users can also apply post-print color coding (painting or labeling) or print separate parts and assemble them manually.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A large FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A multi-material FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Small resin-printed models&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:GABAA_receptor.png|320px|center|thumb| GABAA receptor, [[6x3x]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Bacterial_Ribosome_multimaterial_FDM.png|348px|center|thumb| Bacterial 70S ribosome, [[4v5d]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Dna_insuline_sla.png|252px|center|thumb|DNA (left) and insulin (right) models, [[4bna]] and [[4ins]], scale at the bottom in cm]]&lt;br /&gt;
|-&lt;br /&gt;
|Trace Model of the GABAA receptor printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com] &lt;br /&gt;
|Surface model of the Bacterial 70S ribosome printed on a multi-material capable printer (BambuLab X1C AMS). Blue and violet are ribosomal proteins, orange and yellow are rRNAs, and black is tRNA. Printable files available on [https://www.printables.com/model/1430877-bacterial-70s-ribosome Printables.com]&lt;br /&gt;
|Balls and sticks and cartoon models of DNA (right) and insulin (left)&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== File Formats Used in 3D Printing ===&lt;br /&gt;
Proteopedia supports two export formats for generating printable molecular models:&lt;br /&gt;
*&#039;&#039;&#039;.STL&#039;&#039;&#039; (Stereolithography): the most common and universally compatible format; encodes only surface geometry, without color or texture information.&lt;br /&gt;
*&#039;&#039;&#039;.OBJ&#039;&#039;&#039; (Wavefront Object) with an associated &#039;&#039;&#039;.MTL&#039;&#039;&#039; (Material Template Library) files: includes both geometry and optional color/texture data; useful for color prints.&lt;br /&gt;
&lt;br /&gt;
Another widely adopted file format used in 3D printing is the &#039;&#039;&#039;.3MF&#039;&#039;&#039; (3D Manufacturing Format): a modern open standard that stores geometry, color, and multi-material metadata in a single file—recommended for advanced printers. For a more extensive pros and cons of different 3D printing file formats please see [https://all3dp.com/2/3d-file-format-3d-model-types/ The Main 3D Printing File Formats on all3dp]. &lt;br /&gt;
&lt;br /&gt;
STL is ideal for single-color models and maximum compatibility, while OBJ/MTL is recommended for multi-material workflows. 3MF files will be used in this tutorial to save the model and printing settings. &lt;br /&gt;
&lt;br /&gt;
Support in Proteopedia for these formats is based on the export capabilities of Jmol/JSmol; for details, see [http://wiki.jmol.org/index.php/File_formats/3D_Objects#STL STL] and [http://wiki.jmol.org/index.php/File_formats/3D_Objects#OBJ OBJ]&lt;br /&gt;
&lt;br /&gt;
== Overview of the 3D printing process ==&lt;br /&gt;
3D printing enables the transformation of atomic-level structural data into tangible macromolecular models that can be explored through both sight and touch.  &lt;br /&gt;
The process generally follows several main steps, each requiring specific types of software and hardware.&lt;br /&gt;
[[Image:3D_printing_workflow_v2.png|thumb|left|400px|Overview of the 3D printing workflow for generating physical molecular models.]]&lt;br /&gt;
	&lt;br /&gt;
=== Preparing the structure and generating a printable File ===&lt;br /&gt;
:The first stage involves creating a printable three-dimensional representation of the molecule. Some molecular-graphics programs such as [https://www.pymol.org/ PyMOL], [https://www.rbvi.ucsf.edu/chimerax/ UCSF ChimeraX], [https://molstar.org/Mol*], or [https://jmol.sourceforge.net/ Jmol] can be used not only to visualize a structure (from the Protein Data Bank or other sources), but also to export the resulting geometry in a .STL or .OBJ format. However, the default visualization styles of these programs are &#039;&#039;&#039;&#039;&#039;not directly suitable for 3D printing&#039;&#039;&#039;&#039;&#039;. Therefore, when preparing a model for fabrication, it is important to:&lt;br /&gt;
:* &#039;&#039;&#039;Select an appropriate molecular representation&#039;&#039;&#039; (e.g., surface, cartoon, sticks, spheres) depending on the pedagogical or structural feature you wish to highlight.  &lt;br /&gt;
:* &#039;&#039;&#039;Add struts or connectors&#039;&#039;&#039; to increase the mechanical stability of the model, especially for large complexes or long helices.  &lt;br /&gt;
:* &#039;&#039;&#039;Remove specific struts or pseudobonds&#039;&#039;&#039; when individual components — ligands, subunits, or cofactors — need to remain detachable.  &lt;br /&gt;
:* &#039;&#039;&#039;Adjust thickness&#039;&#039;&#039; of atoms, bonds, helices, and sheets to ensure adequate rigidity and printability (features thinner than the printer’s nozzle diameter or resin resolution may break).  &lt;br /&gt;
:* &#039;&#039;&#039;Apply meaningful coloring&#039;&#039;&#039; when preparing multi-material prints, for instance, to distinguish domains, chains, ligands or atoms.&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene that automates the process and enables users to effortlessly generate 3D-printable molecular models - more on that in the corresponding section [[#Generating printable files on Proteopedia|Generating printable files on Proteopedia]] within this page. For advanced users wanting to do this manually, we highly recommend two guides: &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot; /&amp;gt; and &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
=== Slicing the Model ===&lt;br /&gt;
Before printing, the STL file must be processed by a &#039;&#039;&#039;slicer&#039;&#039;&#039; — specialized software that converts 3D geometry into a series of horizontal layers. The slicer also generates &#039;&#039;&#039;G-code&#039;&#039;&#039;, the set of instructions that control the printer. These commands are printer-specific and include parameters such as extrusion speed, layer thickness, temperature, and movement. Together, they are usually stored as a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;.  &lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an FDM printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;number of perimeters&#039;&#039;&#039;, which affects mechanical strength and print time;&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines resolution and print duration;&lt;br /&gt;
:* &#039;&#039;&#039;infill density&#039;&#039;&#039;, which determines internal strength and affects print time;&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, temporary structures that hold overhanging regions;&lt;br /&gt;
:* &#039;&#039;&#039;print orientation&#039;&#039;&#039;, which influences surface quality, mechanical strength, and the amount of supports required.&lt;br /&gt;
:All these parameters make up a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. In this step, users must also select the material-specific parameters, or apply a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. More details on these profiles are provided later on this page.&lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines vertical resolution and print time; thinner layers produce smoother surfaces but significantly increase printing duration.&lt;br /&gt;
:* &#039;&#039;&#039;exposure time&#039;&#039;&#039;, which controls how long each layer is cured by UV light; optimal exposure ensures proper adhesion between layers without over-curing fine details.&lt;br /&gt;
:* &#039;&#039;&#039;bottom-layer exposure and count&#039;&#039;&#039;, which influence model adhesion to the build platform — longer exposures and additional base layers improve stability during printing.&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, which anchor the model to the build plate and prevent deformation during peeling; proper placement reduces surface marks and print failures.&lt;br /&gt;
:* &#039;&#039;&#039;model orientation&#039;&#039;&#039;, which affects surface quality, support contact area, and resin drainage; angling the model (typically 30–45°) minimizes suction forces and improves print reliability.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for FDM printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for resin printing&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:Insuline_sliced_prusa.gif|386px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|[[Image:Insuline_Sliced_SLA.gif|372px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|-&lt;br /&gt;
|Cartoon model of insulin sliced in PrusaSlicer and ready to be printed on FDM printers. The arrow shows the trajectory of the print head on a single slice or layer. Orange is the model, green are the supports. &lt;br /&gt;
|Cartoon model of insulin sliced in Elegoo SatelLite and ready to be printed on FDM printer.On the left, with blue is the model, with gray are the supports. On the right is the image on the UV screen. &lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== 3D Printing the Model ===&lt;br /&gt;
:The prepared G-code is then transferred to the 3D printer, either via an SD card, USB flash drive, or Wi-Fi connection. During printing, close observation of the first few layers is essential to ensure good adhesion to the build plate and a successful print. Total printing time depends on model size, selected layer height, and printer speed. &#039;&#039;Small peptide&#039;&#039; models may print in &#039;&#039;&#039;less than an hour&#039;&#039;&#039;, whereas l&#039;&#039;arge multimeric assemblies&#039;&#039; can require &#039;&#039;&#039;several hours or days&#039;&#039;&#039;. &#039;&#039;Multi-color&#039;&#039; or &#039;&#039;multi-material&#039;&#039; prints generally take &#039;&#039;&#039;longer&#039;&#039;&#039;, while &#039;&#039;SLA/DLP&#039;&#039; printers are generally &#039;&#039;&#039;faster&#039;&#039;&#039; due to their simultaneous layer exposure.&lt;br /&gt;
=== Post-Processing ===&lt;br /&gt;
:After printing, the model undergoes post-processing, which varies depending on the printing technology used:&lt;br /&gt;
:* For &#039;&#039;&#039;FDM prints&#039;&#039;&#039;, supports are removed mechanically, and surfaces can be smoothed by light sanding or polishing.&lt;br /&gt;
:* For &#039;&#039;&#039;resin prints&#039;&#039;&#039;, supports are removed mechanically, parts are washed in isopropanol to remove uncured resin and then exposed to UV light for final curing.&lt;br /&gt;
:Models printed in multiple parts can be assembled using cyanoacrylate or epoxy adhesive. Optional finishing steps (painting, labeling) can improve contrast between subunits or highlight functional regions.&lt;br /&gt;
&lt;br /&gt;
==Generating printable files on Proteopedia==&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene, enabling logged-in users to effortlessly generate 3D-printable molecular models directly from its pages. The tool is powered by [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;], a script that analyzes the structural data and automatically scales the model’s geometry to match the printable volume of a medium-size desktop 3D printer (e.g., Ender-3, 210×210×210 mm). During this process, the tool evaluates the molecular bounding box, atom radii, and bond lengths, then proportionally adjusts all dimensions to achieve a realistic and mechanically robust print scale — preserving scientific accuracy while ensuring manufacturability. For advanced users, [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;] may also be used in conjunction with the [https://jmol.sourceforge.net/ &#039;&#039;&#039;Jmol&#039;&#039;&#039;] program, providing full access to its scripting capabilities and advanced export features.&lt;br /&gt;
==Step-by-step guide for automatic generation of printable files on Proteopedia==&lt;br /&gt;
=== Open a structure and access the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool ===&lt;br /&gt;
Log in with your Proteopedia Username and password. Navigate to any Proteopedia page (for example, [[Introduction_to_protein_structure]]). The corresponding 3D structure will load in the viewer on the right.  &lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_button_in_Proteopedia.png|thumb|left|400px|The &#039;&#039;&#039;Print3D&#039;&#039;&#039; button on a Proteopedia page]]&lt;br /&gt;
&lt;br /&gt;
At the bottom of the structure display window, locate and click the &#039;&#039;&#039;Print3D&#039;&#039;&#039; button. The tool will launch and begin analyzing the current molecular structure.  &lt;br /&gt;
This process may take some time to complete, depending on the size of the structure.  &lt;br /&gt;
Please wait until the message &#039;&#039;&#039;Analyzing structure...&#039;&#039;&#039; disappears and the next page is displayed — this marks the start of the two-step printing workflow.&lt;br /&gt;
=== Select a molecular representation and a printing scale ===&lt;br /&gt;
In this new page, some user input is required. Each option includes a short explanation; the key steps are outlined below, but feel free to explore and adopt the settings that best fit your use case.&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step1.png|thumb|left|400px|Selecting molecular representation and printing scale]]&lt;br /&gt;
&lt;br /&gt;
(1) &#039;&#039;&#039;Choose a molecular representation&#039;&#039;&#039; from the &#039;&#039;&#039;Scheme&#039;&#039;&#039; list, based on your goal:&lt;br /&gt;
* &#039;&#039;&#039;Backbone&#039;&#039;&#039;, &#039;&#039;&#039;Trace&#039;&#039;&#039;, or &#039;&#039;&#039;Ribbon&#039;&#039;&#039; — to emphasize secondary structure (effective for teaching protein folds).&lt;br /&gt;
* &#039;&#039;&#039;Surface&#039;&#039;&#039; — to highlight molecular topology and binding sites.&lt;br /&gt;
* &#039;&#039;&#039;Ball &amp;amp; Stick&#039;&#039;&#039; — atom-level detail for ligands or small molecules; usually impractical for large proteins or complexes.&lt;br /&gt;
* &#039;&#039;&#039;Proteopedia Scene&#039;&#039;&#039; — attempts to render the current page’s scene directly; may not work for all scenes. This is not fully implemented and only available for a few users.&lt;br /&gt;
&#039;&#039;Note:&#039;&#039; Some representations may be unavailable for a given structure because they are not printable in a reliable way.&lt;br /&gt;
&lt;br /&gt;
(2) In the &#039;&#039;&#039;Printer&#039;&#039;&#039; section, select whether you want a &#039;&#039;&#039;single-color&#039;&#039;&#039; or a &#039;&#039;&#039;multi-color&#039;&#039;&#039; print.&lt;br /&gt;
&lt;br /&gt;
(3) In the &#039;&#039;&#039;Printer scale&#039;&#039;&#039; section, set the desired size of the printed model. The tool constrains safe sizes based on the chosen representation and displays the physical dimensions (mm). &#039;&#039;&#039;Important! Please note the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;printer scale value in %&amp;lt;/span&amp;gt; as it is going to be required downstream in the next section of this workflow, [[#Printing files from Proteopedia|Printing files from Proteopedia]]&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
(4) When ready, click the green &#039;&#039;&#039;Make printer files&#039;&#039;&#039; button. Please wait patiently until the  &#039;&#039;Generating files for 3D printing of...&#039;&#039; message disappears and the final step is displayed.&lt;br /&gt;
&lt;br /&gt;
===Download the .STL or .OBJ files===&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step2.png|thumb|left|400px|Final step in generating printable files]]&lt;br /&gt;
&lt;br /&gt;
In this final page, a 3D preview of the generated model is displayed.&lt;br /&gt;
You can use the mouse to rotate, zoom, and inspect the model from different angles. If the result meets your needs, click the green (A) &#039;&#039;&#039;Download files&#039;&#039;&#039; button and save the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive containing the &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; files on your computer. If your model needs further improvements, hit the green (B) &#039;&#039;&#039;Same structure&#039;&#039;&#039; button to return to the previous screen and adjust your settings.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{clear}}&lt;br /&gt;
== Printing files from Proteopedia ==&lt;br /&gt;
Unzipping the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive will produce the exported &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file, along with an optional &#039;&#039;&#039;.MTL&#039;&#039;&#039; material file. &lt;br /&gt;
=== Using 3D printing services ===&lt;br /&gt;
If you do not have a 3D printer, you can still obtain physical models by using locally available 3D-printing services. Just search on [https://www.google.com/maps Google Maps] with the term  &#039;&#039;&#039;3D printing&#039;&#039;&#039; in your area. Here is short list of well-known 3D Printing service providers that may also ship worldwide: &lt;br /&gt;
&lt;br /&gt;
* [https://www.shapeways.com/ &#039;&#039;&#039;Shapeways&#039;&#039;&#039;] — global service offering a wide range of materials and colors. Educational discounts are available through their academic program.&lt;br /&gt;
* [https://www.sculpteo.com/en/ &#039;&#039;&#039;Sculpteo&#039;&#039;&#039;] — Europe-based provider offering fast turnaround and many printing technologies, including resin and polymer options.&lt;br /&gt;
* [https://www.xometry.com/capabilities/3d-printing-service &#039;&#039;&#039;Xometry&#039;&#039;&#039;] — large international network providing access to industrial-grade printing methods such as FDM, SLA, SLS, and DMLS.&lt;br /&gt;
* [https://craftcloud3d.com/ &#039;&#039;&#039;Craftcloud&#039;&#039;&#039;] — an aggregator that compares multiple providers and finds the best price and lead time for your uploaded model.&lt;br /&gt;
&lt;br /&gt;
When contacting a printing service, provide the exported files together with the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value in %&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ([[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). It is also advisable to share the link to this Proteopedia page so that the operator understands the peculiarities of printing molecular models. &lt;br /&gt;
&lt;br /&gt;
=== Using a desktop 3D printer ===&lt;br /&gt;
&lt;br /&gt;
Before importing the .STL or .OBJ file into your slicer software, it is recommended to inspect and, if necessary, repair the model to ensure printability. Common issues include non-manifold geometry, intersecting faces, and missing surfaces.  The example below demonstrates how to use [https://www.blender.org/ &#039;&#039;&#039;Blender&#039;&#039;&#039;] together with its [https://extensions.blender.org/add-ons/print3d-toolbox/ &#039;&#039;&#039;3D Print Toolbox extension&#039;&#039;&#039;] to improve the printability of the .STL and .OBJ files generated with the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in [[Proteopedia]]. &#039;&#039;&#039;Important note&#039;&#039;&#039;: The repair process is largely automated but may introduce artifacts. Carefully inspect the corrected model for any missing or distorted sections, atoms, or bonds, and determine whether these omissions affect the intended purpose of the printed model.  &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for single color or resin printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for multi-color FDM printing&lt;br /&gt;
|-&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=k6u-5JnoP-c&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=OCisrIZMIDM&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|}  &lt;br /&gt;
&lt;br /&gt;
Once the repaired &#039;&#039;&#039;.STL or .OBJ&#039;&#039;&#039; file is ready, it can be imported into your slicer software. In this step, you will prepare the file for printing by applying appropriate printer, filament, and print-settings profiles.&lt;br /&gt;
&lt;br /&gt;
*Apply the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value (%)&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ( [[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). This step ensures that the model fits your print bed and maintains structural integrity during printing. The location of the scale (%) input field varies depending on the slicer software you are using.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Orient the model on the print bed&#039;&#039;&#039; so that its largest, flattest surface rests on the bed. This minimizes the need for supports and improves adhesion. If your slicer includes an Auto Orient or Auto Arrange function, use it to optimize placement. (&#039;&#039;Hint&#039;&#039;: Bambu Studio and Orca Slicer include this feature, Ultimaker Cura has a [https://marketplace.ultimaker.com/app/cura/plugins/nallath/OrientationPlugin Auto-Orientation plugin] available, while PrusaSlicer currently does not.)&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Select the printer&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that matches your device.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Choose the material&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; corresponding to the filament type (e.g., PLA, PETG, TPU) and manufacturer you intend to use.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Adjust the printing parameters&#039;&#039;&#039; by selecting a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that defines layer height, infill, speed, and support options.&lt;br /&gt;
&lt;br /&gt;
In most cases, the default &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; and &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; provided by the slicer are sufficient. However, molecular models often include overhangs, thin connections, and complex internal geometries, which require additional supports and reinforced perimeters to ensure structural stability. For this reason, the default &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; may not yield optimal results.&lt;br /&gt;
&lt;br /&gt;
Validated printing profiles for the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool are available for several printer models. These profiles provide optimized settings that produce sturdy models, reduce material consumption, and shorten print time, ensuring consistent and reliable results. Three distinct profiles are supplied, corresponding to major molecular representations: &#039;&#039;&#039;balls and sticks&#039;&#039;&#039;, &#039;&#039;&#039;surface&#039;&#039;&#039;, and &#039;&#039;&#039;cartoon&#039;&#039;&#039;. The &#039;&#039;&#039;cartoon&#039;&#039;&#039; profile is also suitable for &#039;&#039;&#039;backbone&#039;&#039;&#039;, &#039;&#039;&#039;trace&#039;&#039;&#039;, and &#039;&#039;&#039;ribbon&#039;&#039;&#039; representations. For some printers, each profile is supplied in two variants, one using standard supports and one using tree or organic supports. In the case of multi-material printers, profiles for printing with soluble support and soluble interface are also provided.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer brand and model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Profiles provided as / Slicer&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer Type, nozle size and multi-material support&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |GitHub with profiles&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to import profiles into Slicer&lt;br /&gt;
|-&lt;br /&gt;
|Original Prusa Core One&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer ]&lt;br /&gt;
|FDM / 0.4 mm / yes, 5 colors, if MMU3 installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/Prusa%20CoreOne CoreOne]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab A1Mini&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, 4 colors if AMS Lite is installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/BambuLab%20A1Mini AiMini]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab X1 Carbon&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, up to 16 colors if multiple AMS are installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ca92e7de9c72505c1b9b09e912ad177341cabc9a/BambuLab%20X1C X1Carbon]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|- &lt;br /&gt;
|Original Prusa MK3S+&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/7a7ee68d1e19f063600f53def49a99dfefbc595d/Prusa%20MK3S%2B MK3S+]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 5 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/a653c7cc6b3dec86b90117cc450d1883cc4a80bd/Ender-5-Pro Ender5Pro]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 3 v2 with a ENDERIDEX kit&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / yes, IDEX, two filaments&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/c2c74f1261a42c160e7e3898a407f21465de2ca7/Ender3-IDEX Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Kingroon KPS3 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ea733b2d05020b99f91c92f71a039c5ba8e54108/Kingroon-KPS3-Pro Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Elegoo Mars 5 Ultra&lt;br /&gt;
|no profile needed, just be sure to add supports / [https://www.elegoo.com/pages/satellite-3d-slicer?srsltid=AfmBOopMQGHgHycHMFOZALzOIC8z7bVlSHjL_jj2ShYR4QkowYKmKzUx ELEGOO SatelLite]&lt;br /&gt;
|resin / - / no&lt;br /&gt;
|&lt;br /&gt;
|no profile needed, default settings worked, just be sure to add supports. EVO supports worked well enough.  Post-processing steps: 1)washing: at least 10 min. 2) support removal 3)curring: at least 10 min on a Elegoo Mercury Plus V3.0&lt;br /&gt;
|- &lt;br /&gt;
|} &lt;br /&gt;
&#039;&#039;&#039;Notes&#039;&#039;&#039;: &lt;br /&gt;
* These profiles were developed and validated with the support of EDUMOL3D, Project [http://cercetare.bio.uaic.ro/grupuri/bioactive/content/grants/PED2024_mm.html PN-IV-P7-7.1-PED-2024-0343] financed by the Ministry of Research, Innovation and Digitization, [https://uefiscdi.gov.ro/ UEFISCDI], Romania.&lt;br /&gt;
* The profiles are a work in progress. Please check GitHub for updates. If you have suggestions for improvements, please drop a message at marius.mihasan(@)uaic.ro&lt;br /&gt;
&lt;br /&gt;
==== &#039;&#039;&#039;Note on multi-color printing &#039;&#039;&#039; ====&lt;br /&gt;
To our knowledge, only &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039; and &#039;&#039;&#039;Orca Slicer&#039;&#039;&#039; can automatically import color information from the &#039;&#039;&#039;.MTL&#039;&#039;&#039; file associated with the printable &#039;&#039;&#039;.OBJ&#039;&#039;&#039; generated by the Proteopedia &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool.  &lt;br /&gt;
At present, &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; does not support importing &#039;&#039;&#039;.MTL&#039;&#039;&#039; files directly.&lt;br /&gt;
&lt;br /&gt;
A practical workaround for &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; users is as follows:  &lt;br /&gt;
# Open the &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file in &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039;.  &lt;br /&gt;
#Verify or adjust the color mapping as needed.  &lt;br /&gt;
#Export the model as a generic &#039;&#039;&#039;.3MF&#039;&#039;&#039; file using the menu command:  &#039;&#039;File&#039;&#039; → &#039;&#039;Export&#039;&#039; → &#039;&#039;Export Generic 3MF...&#039;&#039;  &lt;br /&gt;
#Open the exported &#039;&#039;&#039;.3MF&#039;&#039;&#039; file in &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;. The color data will now be available under the &#039;&#039;&#039;Multimaterial Painting&#039;&#039;&#039; tool.&lt;br /&gt;
&lt;br /&gt;
This workflow preserves the original coloring assigned in Proteopedia and allows successful multi-color or multi-material printing on any capable 3D printer compatible with &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Other relevant resources ==&lt;br /&gt;
[[https://proteopedia.org/w/Print3D_models_gallery Print3d Models gallery]] - examples of 3D printed molecular models from Proteopedia users.&lt;br /&gt;
&lt;br /&gt;
[https://3d.nih.gov/ NIH 3D Print Exchange] - an open, community-driven portal to download, share, and create bioscientific and medical 3D models, including for 3D printing.&lt;br /&gt;
  &lt;br /&gt;
[https://github.com/mariusmihasan/3DP-Jmol 3DP-Jmol] - the Jmol/JSmol behind the Print3D tool. Automatically generates 3D printable molecular models from structural data and can be easily integrated into web pages.&lt;br /&gt;
&lt;br /&gt;
[https://pdb101.rcsb.org/learn/3d-printing/pdb-structures-and-3d-printing 3D Printing on PDB101] - a quick guide on 3D printing molecular models and a small curated 3D models for education&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;If you print a model from Proteopedia, please share photos and feedback — let’s 3D print the whole Proteopedia!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4396886</id>
		<title>Print3D help</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4396886"/>
		<updated>2025-12-01T08:43:59Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== Proteopedia and 3D Printing ==&lt;br /&gt;
&lt;br /&gt;
Physical molecular models, by engaging both visual and tactile senses, provide an effective means of deepening the understanding of complex concepts in molecular biology and biochemistry. They allow students to perceive the three-dimensional organization of macromolecules, thereby enhancing comprehension of the relationship between structure and function &amp;lt;ref&amp;gt;PMID: 32590880&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 40214166&amp;lt;/ref&amp;gt;. Numerous studies have demonstrated that the use of tangible models in science education improves learning outcomes, fosters conceptual reasoning, and increases student engagement &amp;lt;ref&amp;gt;PMID: 27366318&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 26712513&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;Larsson, C., Tibell, L.A.E. Challenging Students’ Intuitions—the Influence of a Tangible Model of Virus Assembly on Students’ Conceptual Reasoning About the Process of Self-Assembly. Res Sci Educ 45, 663–690 (2015). [http://dx.doi.org/10.1007/s11165-014-9446-6 DOI: 110.1007/s11165-014-9446-6]&amp;lt;/ref&amp;gt;. The rapid development of 3D-printing technologies has made it possible to create customized and affordable molecular models  &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot;&amp;gt;PMID: 28362403&amp;lt;/ref&amp;gt; &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot;&amp;gt;PMID: 33755300&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 33384761&amp;lt;/ref&amp;gt;. &lt;br /&gt;
&lt;br /&gt;
Affordable desktop 3D printers can now be used to fabricate physical models from virtually any structure or scene on [[Proteopedia]]. This page provides an introduction to 3D printing, a step-by-step guide to generating printable files directly from [[Proteopedia]], and several tested printing profiles for common printers (e.g., Prusa Research, Bambu Lab, Creality, or Elegoo).&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== «3D Printing 101»: an introduction to 3D printing ==&lt;br /&gt;
3D printing, also known as &#039;&#039;additive manufacturing&#039;&#039;, builds physical objects layer by layer from digital designs. For more technical details please head for the excellent introductory article on [https://all3dp.com/2/what-is-3d-printing/ All3DP].  In structural biology education, 3D printing provides an affordable and accessible way to transform atomic coordinate data (e.g., from PDB, MOL or SDF files) into tangible molecular models that can be observed, handled, and discussed in class or laboratory settings.&lt;br /&gt;
&lt;br /&gt;
=== Printer Types: FDM vs. SLA/DLP ===&lt;br /&gt;
The two most accessible 3D-printing technologies that can be used to create molecular models are:&lt;br /&gt;
* &#039;&#039;&#039;FDM (Fused Deposition Modeling)&#039;&#039;&#039;&lt;br /&gt;
This method extrudes a heated thermoplastic filament (such as PLA, PETG or TPU) through a fine nozzle, depositing successive layers that form the model. FDM printers have the advantages of low cost, easy maintenance, wide availability, and being capable of printing large and colorful molecular models. This technology has a few limitations, such as: visible layer lines, lower surface resolution, and less suited for very small or intricate molecular details.&lt;br /&gt;
* &#039;&#039;&#039;SLA/DLP (Resin Printing)&#039;&#039;&#039;&lt;br /&gt;
This technique uses liquid photopolymer resin, cured layer by layer with ultraviolet light. SLA/DLP printers have the advantages of a very high resolution, smooth surfaces and are ideal for compact and detailed models (e.g., small proteins rendered as surface, ligands, or symmetric assemblies). This technology has its own limitations, such as higher material cost, post-processing requirements (washing and UV-curing), and the need for careful handling of resin.&lt;br /&gt;
&lt;br /&gt;
When choosing between FDM and SLA printers, model size and resolution are the key criteria: &#039;&#039;&#039;FDM&#039;&#039;&#039; is preferred for &#039;&#039;large, educational display models&#039;&#039;; &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; is optimal for &#039;&#039;small, precise structures&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
While FDM and SLA/DLP are the most widely used technologies in educational and research contexts due to their accessibility, other additive manufacturing methods also exist —such as &#039;&#039;Selective Laser Sintering&#039;&#039; (SLS), &#039;&#039;PolyJet&#039;&#039;, and &#039;&#039;Binder Jetting&#039;&#039;— each employing different materials and curing mechanisms. These industrial-grade techniques can produce highly detailed or multi-material parts but are generally more expensive and less accessible for classroom use. For an overview of major 3D-printing technologies, see [https://all3dp.com/1/types-of-3d-printers-3d-printing-technology/ All3DP: Complete Overview of the Types of 3D Printers]&lt;br /&gt;
&lt;br /&gt;
=== Single- vs. Multi-Material Printers ===&lt;br /&gt;
Most entry-level desktop 3D printers use a single filament or resin, producing models in one color or material. However, multi-material systems (such as [https://eu.store.bambulab.com/products/ams-multicolor-printing?from=home_web_top_navigation Bambu Lab AMS] and its variants or [https://www.prusa3d.com/category/original-prusa-mmu3/ Prusa MMU3]) can simultaneously print multiple filaments, enabling color-coded domains, subunits, or ligands directly in one print. For complex color information, users can also apply post-print color coding (painting or labeling) or print separate parts and assemble them manually.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A large FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A multi-material FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Small resin-printed models&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:GABAA_receptor.png|320px|center|thumb| GABAA receptor, [[6x3x]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Bacterial_Ribosome_multimaterial_FDM.png|348px|center|thumb| Bacterial 70S ribosome, [[4v5d]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Dna_insuline_sla.png|252px|center|thumb|DNA (left) and insulin (right) models, [[4bna]] and [[4ins]], scale at the bottom in cm]]&lt;br /&gt;
|-&lt;br /&gt;
|Trace Model of the GABAA receptor printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com] &lt;br /&gt;
|Surface model of the Bacterial 70S ribosome printed on a multi-material capable printer (BambuLab X1C AMS). Blue and violet are ribosomal proteins, orange and yellow are rRNAs, and black is tRNA. Printable files available on [https://www.printables.com/model/1430877-bacterial-70s-ribosome Printables.com]&lt;br /&gt;
|Balls and sticks and cartoon models of DNA (right) and insulin (left)&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== File Formats Used in 3D Printing ===&lt;br /&gt;
Proteopedia supports two export formats for generating printable molecular models:&lt;br /&gt;
*&#039;&#039;&#039;.STL&#039;&#039;&#039; (Stereolithography): the most common and universally compatible format; encodes only surface geometry, without color or texture information.&lt;br /&gt;
*&#039;&#039;&#039;.OBJ&#039;&#039;&#039; (Wavefront Object) with an associated &#039;&#039;&#039;.MTL&#039;&#039;&#039; (Material Template Library) files: includes both geometry and optional color/texture data; useful for color prints.&lt;br /&gt;
&lt;br /&gt;
Another widely adopted file format used in 3D printing is the &#039;&#039;&#039;.3MF&#039;&#039;&#039; (3D Manufacturing Format): a modern open standard that stores geometry, color, and multi-material metadata in a single file—recommended for advanced printers. For a more extensive pros and cons of different 3D printing file formats please see [https://all3dp.com/2/3d-file-format-3d-model-types/ The Main 3D Printing File Formats on all3dp]. &lt;br /&gt;
&lt;br /&gt;
STL is ideal for single-color models and maximum compatibility, while OBJ/MTL is recommended for multi-material workflows. 3MF files will be used in this tutorial to save the model and printing settings. &lt;br /&gt;
&lt;br /&gt;
Support in Proteopedia for these formats is based on the export capabilities of Jmol/JSmol; for details, see [http://wiki.jmol.org/index.php/File_formats/3D_Objects#STL STL] and [http://wiki.jmol.org/index.php/File_formats/3D_Objects#OBJ OBJ]&lt;br /&gt;
&lt;br /&gt;
== Overview of the 3D printing process ==&lt;br /&gt;
3D printing enables the transformation of atomic-level structural data into tangible macromolecular models that can be explored through both sight and touch.  &lt;br /&gt;
The process generally follows several main steps, each requiring specific types of software and hardware.&lt;br /&gt;
[[Image:3D_printing_workflow_v2.png|thumb|left|400px|Overview of the 3D printing workflow for generating physical molecular models.]]&lt;br /&gt;
	&lt;br /&gt;
=== Preparing the structure and generating a printable File ===&lt;br /&gt;
:The first stage involves creating a printable three-dimensional representation of the molecule. Some molecular-graphics programs such as [https://www.pymol.org/ PyMOL], [https://www.rbvi.ucsf.edu/chimerax/ UCSF ChimeraX], [https://molstar.org/Mol*], or [https://jmol.sourceforge.net/ Jmol] can be used not only to visualize a structure (from the Protein Data Bank or other sources), but also to export the resulting geometry in a .STL or .OBJ format. However, the default visualization styles of these programs are &#039;&#039;&#039;&#039;&#039;not directly suitable for 3D printing&#039;&#039;&#039;&#039;&#039;. Therefore, when preparing a model for fabrication, it is important to:&lt;br /&gt;
:* &#039;&#039;&#039;Select an appropriate molecular representation&#039;&#039;&#039; (e.g., surface, cartoon, sticks, spheres) depending on the pedagogical or structural feature you wish to highlight.  &lt;br /&gt;
:* &#039;&#039;&#039;Add struts or connectors&#039;&#039;&#039; to increase the mechanical stability of the model, especially for large complexes or long helices.  &lt;br /&gt;
:* &#039;&#039;&#039;Remove specific struts or pseudobonds&#039;&#039;&#039; when individual components — ligands, subunits, or cofactors — need to remain detachable.  &lt;br /&gt;
:* &#039;&#039;&#039;Adjust thickness&#039;&#039;&#039; of atoms, bonds, helices, and sheets to ensure adequate rigidity and printability (features thinner than the printer’s nozzle diameter or resin resolution may break).  &lt;br /&gt;
:* &#039;&#039;&#039;Apply meaningful coloring&#039;&#039;&#039; when preparing multi-material prints, for instance, to distinguish domains, chains, ligands or atoms.&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene that automates the process and enables users to effortlessly generate 3D-printable molecular models - more on that in the corresponding section [[#Generating printable files on Proteopedia|Generating printable files on Proteopedia]] within this page. For advanced users wanting to do this manually, we highly recommend two guides: &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot; /&amp;gt; and &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
=== Slicing the Model ===&lt;br /&gt;
Before printing, the STL file must be processed by a &#039;&#039;&#039;slicer&#039;&#039;&#039; — specialized software that converts 3D geometry into a series of horizontal layers. The slicer also generates &#039;&#039;&#039;G-code&#039;&#039;&#039;, the set of instructions that control the printer. These commands are printer-specific and include parameters such as extrusion speed, layer thickness, temperature, and movement. Together, they are usually stored as a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;.  &lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an FDM printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;number of perimeters&#039;&#039;&#039;, which affects mechanical strength and print time;&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines resolution and print duration;&lt;br /&gt;
:* &#039;&#039;&#039;infill density&#039;&#039;&#039;, which determines internal strength and affects print time;&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, temporary structures that hold overhanging regions;&lt;br /&gt;
:* &#039;&#039;&#039;print orientation&#039;&#039;&#039;, which influences surface quality, mechanical strength, and the amount of supports required.&lt;br /&gt;
:All these parameters make up a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. In this step, users must also select the material-specific parameters, or apply a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. More details on these profiles are provided later on this page.&lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines vertical resolution and print time; thinner layers produce smoother surfaces but significantly increase printing duration.&lt;br /&gt;
:* &#039;&#039;&#039;exposure time&#039;&#039;&#039;, which controls how long each layer is cured by UV light; optimal exposure ensures proper adhesion between layers without over-curing fine details.&lt;br /&gt;
:* &#039;&#039;&#039;bottom-layer exposure and count&#039;&#039;&#039;, which influence model adhesion to the build platform — longer exposures and additional base layers improve stability during printing.&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, which anchor the model to the build plate and prevent deformation during peeling; proper placement reduces surface marks and print failures.&lt;br /&gt;
:* &#039;&#039;&#039;model orientation&#039;&#039;&#039;, which affects surface quality, support contact area, and resin drainage; angling the model (typically 30–45°) minimizes suction forces and improves print reliability.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for FDM printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for resin printing&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:Insuline_sliced_prusa.gif|386px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|[[Image:Insuline_Sliced_SLA.gif|372px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|-&lt;br /&gt;
|Cartoon model of insulin sliced in PrusaSlicer and ready to be printed on FDM printers. The arrow shows the trajectory of the print head on a single slice or layer. Orange is the model, green are the supports. &lt;br /&gt;
|Cartoon model of insulin sliced in Elegoo SatelLite and ready to be printed on FDM printer.On the left, with blue is the model, with gray are the supports. On the right is the image on the UV screen. &lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== 3D Printing the Model ===&lt;br /&gt;
:The prepared G-code is then transferred to the 3D printer, either via an SD card, USB flash drive, or Wi-Fi connection. During printing, close observation of the first few layers is essential to ensure good adhesion to the build plate and a successful print. Total printing time depends on model size, selected layer height, and printer speed. &#039;&#039;Small peptide&#039;&#039; models may print in &#039;&#039;&#039;less than an hour&#039;&#039;&#039;, whereas l&#039;&#039;arge multimeric assemblies&#039;&#039; can require &#039;&#039;&#039;several hours or days&#039;&#039;&#039;. &#039;&#039;Multi-color&#039;&#039; or &#039;&#039;multi-material&#039;&#039; prints generally take &#039;&#039;&#039;longer&#039;&#039;&#039;, while &#039;&#039;SLA/DLP&#039;&#039; printers are generally &#039;&#039;&#039;faster&#039;&#039;&#039; due to their simultaneous layer exposure.&lt;br /&gt;
=== Post-Processing ===&lt;br /&gt;
:After printing, the model undergoes post-processing, which varies depending on the printing technology used:&lt;br /&gt;
:* For &#039;&#039;&#039;FDM prints&#039;&#039;&#039;, supports are removed mechanically, and surfaces can be smoothed by light sanding or polishing.&lt;br /&gt;
:* For &#039;&#039;&#039;resin prints&#039;&#039;&#039;, supports are removed mechanically, parts are washed in isopropanol to remove uncured resin and then exposed to UV light for final curing.&lt;br /&gt;
:Models printed in multiple parts can be assembled using cyanoacrylate or epoxy adhesive. Optional finishing steps (painting, labeling) can improve contrast between subunits or highlight functional regions.&lt;br /&gt;
&lt;br /&gt;
==Generating printable files on Proteopedia==&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene, enabling logged-in users to effortlessly generate 3D-printable molecular models directly from its pages. The tool is powered by [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;], a script that analyzes the structural data and automatically scales the model’s geometry to match the printable volume of a medium-size desktop 3D printer (e.g., Ender-3, 210×210×210 mm). During this process, the tool evaluates the molecular bounding box, atom radii, and bond lengths, then proportionally adjusts all dimensions to achieve a realistic and mechanically robust print scale — preserving scientific accuracy while ensuring manufacturability. For advanced users, [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;] may also be used in conjunction with the [https://jmol.sourceforge.net/ &#039;&#039;&#039;Jmol&#039;&#039;&#039;] program, providing full access to its scripting capabilities and advanced export features.&lt;br /&gt;
==Step-by-step guide for automatic generation of printable files on Proteopedia==&lt;br /&gt;
=== Open a structure and access the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool ===&lt;br /&gt;
Log in with your Proteopedia Username and password. Navigate to any Proteopedia page (for example, [[Introduction_to_protein_structure]]). The corresponding 3D structure will load in the viewer on the right.  &lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_button_in_Proteopedia.png|thumb|left|400px|The &#039;&#039;&#039;Print3D&#039;&#039;&#039; button on a Proteopedia page]]&lt;br /&gt;
&lt;br /&gt;
At the bottom of the structure display window, locate and click the &#039;&#039;&#039;Print3D&#039;&#039;&#039; button. The tool will launch and begin analyzing the current molecular structure.  &lt;br /&gt;
This process may take some time to complete, depending on the size of the structure.  &lt;br /&gt;
Please wait until the message &#039;&#039;&#039;Analyzing structure...&#039;&#039;&#039; disappears and the next page is displayed — this marks the start of the two-step printing workflow.&lt;br /&gt;
=== Select a molecular representation and a printing scale ===&lt;br /&gt;
In this new page, some user input is required. Each option includes a short explanation; the key steps are outlined below, but feel free to explore and adopt the settings that best fit your use case.&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step1.png|thumb|left|400px|Selecting molecular representation and printing scale]]&lt;br /&gt;
&lt;br /&gt;
(1) &#039;&#039;&#039;Choose a molecular representation&#039;&#039;&#039; from the &#039;&#039;&#039;Scheme&#039;&#039;&#039; list, based on your goal:&lt;br /&gt;
* &#039;&#039;&#039;Backbone&#039;&#039;&#039;, &#039;&#039;&#039;Trace&#039;&#039;&#039;, or &#039;&#039;&#039;Ribbon&#039;&#039;&#039; — to emphasize secondary structure (effective for teaching protein folds).&lt;br /&gt;
* &#039;&#039;&#039;Surface&#039;&#039;&#039; — to highlight molecular topology and binding sites.&lt;br /&gt;
* &#039;&#039;&#039;Ball &amp;amp; Stick&#039;&#039;&#039; — atom-level detail for ligands or small molecules; usually impractical for large proteins or complexes.&lt;br /&gt;
* &#039;&#039;&#039;Proteopedia Scene&#039;&#039;&#039; — attempts to render the current page’s scene directly; may not work for all scenes. This is not fully implemented and only available for a few users.&lt;br /&gt;
&#039;&#039;Note:&#039;&#039; Some representations may be unavailable for a given structure because they are not printable in a reliable way.&lt;br /&gt;
&lt;br /&gt;
(2) In the &#039;&#039;&#039;Printer&#039;&#039;&#039; section, select whether you want a &#039;&#039;&#039;single-color&#039;&#039;&#039; or a &#039;&#039;&#039;multi-color&#039;&#039;&#039; print.&lt;br /&gt;
&lt;br /&gt;
(3) In the &#039;&#039;&#039;Printer scale&#039;&#039;&#039; section, set the desired size of the printed model. The tool constrains safe sizes based on the chosen representation and displays the physical dimensions (mm). &#039;&#039;&#039;Important! Please note the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;printer scale value in %&amp;lt;/span&amp;gt; as it is going to be required downstream in the next section of this workflow, [[#Printing files from Proteopedia|Printing files from Proteopedia]]&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
(4) When ready, click the green &#039;&#039;&#039;Make printer files&#039;&#039;&#039; button. Please wait patiently until the  &#039;&#039;Generating files for 3D printing of...&#039;&#039; message disappears and the final step is displayed.&lt;br /&gt;
&lt;br /&gt;
===Download the .STL or .OBJ files===&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step2.png|thumb|left|400px|Final step in generating printable files]]&lt;br /&gt;
&lt;br /&gt;
In this final page, a 3D preview of the generated model is displayed.&lt;br /&gt;
You can use the mouse to rotate, zoom, and inspect the model from different angles. If the result meets your needs, click the green (A) &#039;&#039;&#039;Download files&#039;&#039;&#039; button and save the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive containing the &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; files on your computer. If your model needs further improvements, hit the green (B) &#039;&#039;&#039;Same structure&#039;&#039;&#039; button to return to the previous screen and adjust your settings.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{clear}}&lt;br /&gt;
== Printing files from Proteopedia ==&lt;br /&gt;
Unzipping the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive will produce the exported &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file, along with an optional &#039;&#039;&#039;.MTL&#039;&#039;&#039; material file. &lt;br /&gt;
=== Using 3D printing services ===&lt;br /&gt;
If you do not have a 3D printer, you can still obtain physical models by using locally available 3D-printing services. Just search on [https://www.google.com/maps Google Maps] with the term  &#039;&#039;&#039;3D printing&#039;&#039;&#039; in your area. Here is short list of well-known 3D Printing service providers that may also ship worldwide: &lt;br /&gt;
&lt;br /&gt;
* [https://www.shapeways.com/ &#039;&#039;&#039;Shapeways&#039;&#039;&#039;] — global service offering a wide range of materials and colors. Educational discounts are available through their academic program.&lt;br /&gt;
* [https://www.sculpteo.com/en/ &#039;&#039;&#039;Sculpteo&#039;&#039;&#039;] — Europe-based provider offering fast turnaround and many printing technologies, including resin and polymer options.&lt;br /&gt;
* [https://www.xometry.com/capabilities/3d-printing-service &#039;&#039;&#039;Xometry&#039;&#039;&#039;] — large international network providing access to industrial-grade printing methods such as FDM, SLA, SLS, and DMLS.&lt;br /&gt;
* [https://craftcloud3d.com/ &#039;&#039;&#039;Craftcloud&#039;&#039;&#039;] — an aggregator that compares multiple providers and finds the best price and lead time for your uploaded model.&lt;br /&gt;
&lt;br /&gt;
When contacting a printing service, provide the exported files together with the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value in %&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ([[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). It is also advisable to share the link to this Proteopedia page so that the operator understands the peculiarities of printing molecular models. &lt;br /&gt;
&lt;br /&gt;
=== Using a desktop 3D printer ===&lt;br /&gt;
&lt;br /&gt;
Before importing the .STL or .OBJ file into your slicer software, it is recommended to inspect and, if necessary, repair the model to ensure printability. Common issues include non-manifold geometry, intersecting faces, and missing surfaces.  The example below demonstrates how to use [https://www.blender.org/ &#039;&#039;&#039;Blender&#039;&#039;&#039;] together with its [https://extensions.blender.org/add-ons/print3d-toolbox/ &#039;&#039;&#039;3D Print Toolbox extension&#039;&#039;&#039;] to improve the printability of the .STL and .OBJ files generated with the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in [[Proteopedia]]. &#039;&#039;&#039;Important note&#039;&#039;&#039;: The repair process is largely automated but may introduce artifacts. Carefully inspect the corrected model for any missing or distorted sections, atoms, or bonds, and determine whether these omissions affect the intended purpose of the printed model.  &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for single color or resin printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for multi-color FDM printing&lt;br /&gt;
|-&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=k6u-5JnoP-c&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=OCisrIZMIDM&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|}  &lt;br /&gt;
&lt;br /&gt;
Once the repaired &#039;&#039;&#039;.STL or .OBJ&#039;&#039;&#039; file is ready, it can be imported into your slicer software. In this step, you will prepare the file for printing by applying appropriate printer, filament, and print-settings profiles.&lt;br /&gt;
&lt;br /&gt;
*Apply the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value (%)&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ( [[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). This step ensures that the model fits your print bed and maintains structural integrity during printing. The location of the scale (%) input field varies depending on the slicer software you are using.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Orient the model on the print bed&#039;&#039;&#039; so that its largest, flattest surface rests on the bed. This minimizes the need for supports and improves adhesion. If your slicer includes an Auto Orient or Auto Arrange function, use it to optimize placement. (&#039;&#039;Hint&#039;&#039;: Bambu Studio and Orca Slicer include this feature, Ultimaker Cura has a [https://marketplace.ultimaker.com/app/cura/plugins/nallath/OrientationPlugin Auto-Orientation plugin] available, while PrusaSlicer currently does not.)&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Select the printer&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that matches your device.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Choose the material&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; corresponding to the filament type (e.g., PLA, PETG, TPU) and manufacturer you intend to use.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Adjust the printing parameters&#039;&#039;&#039; by selecting a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that defines layer height, infill, speed, and support options.&lt;br /&gt;
&lt;br /&gt;
In most cases, the default &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; and &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; provided by the slicer are sufficient. However, molecular models often include overhangs, thin connections, and complex internal geometries, which require additional supports and reinforced perimeters to ensure structural stability. For this reason, the default &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; may not yield optimal results.&lt;br /&gt;
&lt;br /&gt;
Validated printing profiles for the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool are available for several printer models. These profiles provide optimized settings that produce sturdy models, reduce material consumption, and shorten print time, ensuring consistent and reliable results. Three distinct profiles are supplied, corresponding to major molecular representations: &#039;&#039;&#039;balls and sticks&#039;&#039;&#039;, &#039;&#039;&#039;surface&#039;&#039;&#039;, and &#039;&#039;&#039;cartoon&#039;&#039;&#039;. The &#039;&#039;&#039;cartoon&#039;&#039;&#039; profile is also suitable for &#039;&#039;&#039;backbone&#039;&#039;&#039;, &#039;&#039;&#039;trace&#039;&#039;&#039;, and &#039;&#039;&#039;ribbon&#039;&#039;&#039; representations. For some printers, each profile is supplied in two variants, one using standard supports and one using tree or organic supports. In the case of multi-material printers, profiles for printing with soluble support and soluble interface are also provided.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer brand and model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Profiles provided as / Slicer&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer Type, nozle size and multi-material support&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |GitHub with profiles&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to import profiles into Slicer&lt;br /&gt;
|-&lt;br /&gt;
|Original Prusa Core One&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer ]&lt;br /&gt;
|FDM / 0.4 mm / yes, 5 colors, if MMU3 installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/Prusa%20CoreOne CoreOne]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab A1Mini&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, 4 colors if AMS Lite is installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/BambuLab%20A1Mini AiMini]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab X1 Carbon&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, up to 16 colors if multiple AMS are installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ca92e7de9c72505c1b9b09e912ad177341cabc9a/BambuLab%20X1C X1Carbon]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|- &lt;br /&gt;
|Original Prusa MK3S+&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/7a7ee68d1e19f063600f53def49a99dfefbc595d/Prusa%20MK3S%2B MK3S+]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 5 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/a653c7cc6b3dec86b90117cc450d1883cc4a80bd/Ender-5-Pro Ender5Pro]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 3 v2 with a ENDERIDEX kit&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / yes, IDEX, two filaments&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/c2c74f1261a42c160e7e3898a407f21465de2ca7/Ender3-IDEX Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Kingroon KPS3 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ea733b2d05020b99f91c92f71a039c5ba8e54108/Kingroon-KPS3-Pro Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Elegoo Mars 5 Ultra&lt;br /&gt;
|no profile needed, just be sure to add supports / [https://www.elegoo.com/pages/satellite-3d-slicer?srsltid=AfmBOopMQGHgHycHMFOZALzOIC8z7bVlSHjL_jj2ShYR4QkowYKmKzUx ELEGOO SatelLite]&lt;br /&gt;
|resin / - / no&lt;br /&gt;
|&lt;br /&gt;
|no profile needed, default settings worked, just be sure to add supports. EVO supports worked well enough.  Post-processing steps: 1)washing: at least 10 min. 2) support removal 3)curring: at least 10 min on a Elegoo Mercury Plus V3.0&lt;br /&gt;
|- &lt;br /&gt;
|} &lt;br /&gt;
&#039;&#039;&#039;Notes&#039;&#039;&#039;: &lt;br /&gt;
* These profiles were developed and validated with the support of EDUMOL3D, Project [http://cercetare.bio.uaic.ro/grupuri/bioactive/content/grants/PED2024_mm.html PN-IV-P7-7.1-PED-2024-0343] financed by the Ministry of Research, Innovation and Digitization, [https://uefiscdi.gov.ro/ UEFISCDI], Romania.&lt;br /&gt;
* The profiles are a work in progress. Please check GitHub for updates. If you have suggestions for improvements, please drop a message at marius.mihasan(@)uaic.ro&lt;br /&gt;
&lt;br /&gt;
==== &#039;&#039;&#039;Note on multi-color printing &#039;&#039;&#039; ====&lt;br /&gt;
To our knowledge, only &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039; and &#039;&#039;&#039;Orca Slicer&#039;&#039;&#039; can automatically import color information from the &#039;&#039;&#039;.MTL&#039;&#039;&#039; file associated with the printable &#039;&#039;&#039;.OBJ&#039;&#039;&#039; generated by the Proteopedia &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool.  &lt;br /&gt;
At present, &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; does not support importing &#039;&#039;&#039;.MTL&#039;&#039;&#039; files directly.&lt;br /&gt;
&lt;br /&gt;
A practical workaround for &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; users is as follows:  &lt;br /&gt;
# Open the &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file in &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039;.  &lt;br /&gt;
#Verify or adjust the color mapping as needed.  &lt;br /&gt;
#Export the model as a generic &#039;&#039;&#039;.3MF&#039;&#039;&#039; file using the menu command:  &#039;&#039;File&#039;&#039; → &#039;&#039;Export&#039;&#039; → &#039;&#039;Export Generic 3MF...&#039;&#039;  &lt;br /&gt;
#Open the exported &#039;&#039;&#039;.3MF&#039;&#039;&#039; file in &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;. The color data will now be available under the &#039;&#039;&#039;Multimaterial Painting&#039;&#039;&#039; tool.&lt;br /&gt;
&lt;br /&gt;
This workflow preserves the original coloring assigned in Proteopedia and allows successful multi-color or multi-material printing on any capable 3D printer compatible with &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Other relevant resources ==&lt;br /&gt;
[[https://proteopedia.org/w/Print3D_models_gallery]] - examples of 3D printed molecular models from Proteopedia users.&lt;br /&gt;
&lt;br /&gt;
[https://3d.nih.gov/ NIH 3D Print Exchange] - an open, community-driven portal to download, share, and create bioscientific and medical 3D models, including for 3D printing.&lt;br /&gt;
  &lt;br /&gt;
[https://github.com/mariusmihasan/3DP-Jmol 3DP-Jmol] - the Jmol/JSmol behind the Print3D tool. Automatically generates 3D printable molecular models from structural data and can be easily integrated into web pages.&lt;br /&gt;
&lt;br /&gt;
[https://pdb101.rcsb.org/learn/3d-printing/pdb-structures-and-3d-printing 3D Printing on PDB101] - a quick guide on 3D printing molecular models and a small curated 3D models for education&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;If you print a model from Proteopedia, please share photos and feedback — let’s 3D print the whole Proteopedia!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Adeno-Associated_Virus&amp;diff=4395866</id>
		<title>Adeno-Associated Virus</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Adeno-Associated_Virus&amp;diff=4395866"/>
		<updated>2025-11-28T14:56:28Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==3D Printed Physical Models of an Adeno-Associated Virus==&lt;br /&gt;
&lt;br /&gt;
Shown below are 3D printed physical models of the Adeno-Associated Virus, based on the structure [http://proteopedia.org/wiki/index.php/3ux1 3ux1.pdb]. The capsid is colored by radial distance from the center of the sphere. It has been designed with embedded magnets to dock to a display base.&lt;br /&gt;
&lt;br /&gt;
[[Image:adenoAssociatedVirus_1_centerForBiomolecularModeling.jpg | 500px]] &lt;br /&gt;
[[Image:adenoAssociatedVirus_2_centerForBiomolecularModeling.jpg | 500px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
====The MSOE Center for BioMolecular Modeling====&lt;br /&gt;
&lt;br /&gt;
[[Image:CbmUniversityLogo.jpg | left | 100px]]&lt;br /&gt;
&lt;br /&gt;
The [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling] uses 3D printing technology to create physical models of protein and molecular structures, making the invisible molecular world more tangible and comprehensible. To view more protein structure models, visit our [http://cbm.msoe.edu/educationalmedia/modelgallery/ Model Gallery].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
This is a sample scene created with SAT to &amp;lt;scene name=&amp;quot;/12/3456/Sample/1&amp;quot;&amp;gt;color&amp;lt;/scene&amp;gt; by Group, and another to make &amp;lt;scene name=&amp;quot;/12/3456/Sample/2&amp;quot;&amp;gt;a transparent representation&amp;lt;/scene&amp;gt; of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Electron_Transport_Chain&amp;diff=4395865</id>
		<title>Electron Transport Chain</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Electron_Transport_Chain&amp;diff=4395865"/>
		<updated>2025-11-28T14:55:47Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==3D Printed Physical Model of the Respiration Electron Transport Chain==&lt;br /&gt;
&lt;br /&gt;
Shown below is a 3D printed physical model of the Respiration Electron Transport Chain. Complex I is colored red, complex II is purple, complex III is green, complex IV is blue and the atp synthetase protein is colored orange, yellow and red.&lt;br /&gt;
&lt;br /&gt;
[[Image:atpSynthase_1_centerForBiomolecularModeling.jpg | 750px]] &lt;br /&gt;
&lt;br /&gt;
====The MSOE Center for BioMolecular Modeling====&lt;br /&gt;
&lt;br /&gt;
[[Image:CbmUniversityLogo.jpg | left | 100px]]&lt;br /&gt;
&lt;br /&gt;
The [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling] uses 3D printing technology to create physical models of protein and molecular structures, making the invisible molecular world more tangible and comprehensible. To view more protein structure models, visit our [http://cbm.msoe.edu/educationalmedia/modelgallery/ Model Gallery].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
This is a sample scene created with SAT to &amp;lt;scene name=&amp;quot;/12/3456/Sample/1&amp;quot;&amp;gt;color&amp;lt;/scene&amp;gt; by Group, and another to make &amp;lt;scene name=&amp;quot;/12/3456/Sample/2&amp;quot;&amp;gt;a transparent representation&amp;lt;/scene&amp;gt; of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Glucose_transport_protein&amp;diff=4395864</id>
		<title>Glucose transport protein</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Glucose_transport_protein&amp;diff=4395864"/>
		<updated>2025-11-28T14:52:04Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==3D Printed Physical Model of Glucose Transport Protein (GLUT)==&lt;br /&gt;
&lt;br /&gt;
Shown below are 3D printed physical models of the Glucose Transport Protein (GLUT). The backbone model on the left is colored by repeat regions, with the first half red and the second half blue.  The spacefill model on the right is colored by atom type, with carbon gray, oxygen red, nitrogen blue and sulfur yellow.  &lt;br /&gt;
&lt;br /&gt;
[[Image:glut1_centerForBioMolecularModeling.jpg|550px]]&lt;br /&gt;
&lt;br /&gt;
====The MSOE Center for BioMolecular Modeling====&lt;br /&gt;
&lt;br /&gt;
[[Image:CbmUniversityLogo.jpg | left | 150px]]&lt;br /&gt;
&lt;br /&gt;
The [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling] uses 3D printing technology to create physical models of protein and molecular structures, making the invisible molecular world more tangible and comprehensible. To view more protein structure models, visit our [http://cbm.msoe.edu/educationalmedia/modelgallery/ Model Gallery].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
This is a sample scene created with SAT to &amp;lt;scene name=&amp;quot;/12/3456/Sample/1&amp;quot;&amp;gt;color&amp;lt;/scene&amp;gt; by Group, and another to make &amp;lt;scene name=&amp;quot;/12/3456/Sample/2&amp;quot;&amp;gt;a transparent representation&amp;lt;/scene&amp;gt; of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=User:Karsten_Theis/RNaseA_physical_model_explanation&amp;diff=4395863</id>
		<title>User:Karsten Theis/RNaseA physical model explanation</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=User:Karsten_Theis/RNaseA_physical_model_explanation&amp;diff=4395863"/>
		<updated>2025-11-28T14:50:39Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Introduction==&lt;br /&gt;
This proteopedia page is intended as a companion to a physical model of RNase A used for teaching protein folding and structure at Westfield State University. &lt;br /&gt;
&lt;br /&gt;
[[Image:RNAseA model.jpg|300px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Mark Hoelzer from the MSOE Center for Biomolecular Modeling [https://www.centerforbiomolecularmodeling.org/about] designed, printed and painted the model. Having the model in your hand is great because you can experience the structure in a very direct way, and having this companion page is great because you can see the model even if you do not have the physical model in your hand. It also allows you to hover over different parts of the model with a mouse to get more information (try it after turning off spinning with the +/- spin button!).&lt;br /&gt;
&lt;br /&gt;
==Tour of the structure==&lt;br /&gt;
&amp;lt;StructureSection load=&#039;&#039; size=&#039;340&#039; side=&#039;right&#039; caption=&#039;Caption for this structure&#039; scene=&#039;78/785360/Physmodel/1&#039;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==What the model shows==&lt;br /&gt;
&lt;br /&gt;
===Trace of alpha carbon atoms===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&amp;lt;jmolLink&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;  select (*.CB and not *%B) or (GLY.CA and not *%B); label &amp;quot;%r&amp;quot;; color label black;&lt;br /&gt;
  &amp;lt;/script&amp;gt;&lt;br /&gt;
  &amp;lt;text&amp;gt;label residues&amp;lt;/text&amp;gt;&lt;br /&gt;
&amp;lt;/jmolLink&amp;gt;&amp;lt;/jmol&amp;gt; (click +/- labels to turn off again)&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Hydrogen bonds===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&amp;lt;jmolLink&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;  select all; color hbonds blue; delay 0.8; color hbonds [xCFd0FF]&lt;br /&gt;
  &amp;lt;/script&amp;gt;&lt;br /&gt;
  &amp;lt;text&amp;gt;highlight hydrogen bonds&amp;lt;/text&amp;gt;&lt;br /&gt;
&amp;lt;/jmolLink&amp;gt;&amp;lt;/jmol&amp;gt; &lt;br /&gt;
&lt;br /&gt;
===N-terminus and C-terminus===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&amp;lt;jmolLink&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;  select 1.CA; spacefill 200%; delay 0.8; spacefill off;&lt;br /&gt;
  &amp;lt;/script&amp;gt;&lt;br /&gt;
  &amp;lt;text&amp;gt;N-terminus&amp;lt;/text&amp;gt;&lt;br /&gt;
&amp;lt;/jmolLink&amp;gt;&amp;lt;/jmol&amp;gt; and &amp;lt;jmol&amp;gt;&amp;lt;jmolLink&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;  select 124.CA; spacefill 200%; delay 0.8; spacefill off;&lt;br /&gt;
  &amp;lt;/script&amp;gt;&lt;br /&gt;
  &amp;lt;text&amp;gt;C-terminus&amp;lt;/text&amp;gt;&lt;br /&gt;
&amp;lt;/jmolLink&amp;gt;&amp;lt;/jmol&amp;gt; refer to...&lt;br /&gt;
&lt;br /&gt;
===Disulfide bridges===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&amp;lt;jmolLink&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;  select sidechain and Cys and not Cys%B; spacefill 150%; delay 0.8; spacefill 75%;&lt;br /&gt;
  &amp;lt;/script&amp;gt;&lt;br /&gt;
  &amp;lt;text&amp;gt;Disulfide bridges&amp;lt;/text&amp;gt;&lt;br /&gt;
&amp;lt;/jmolLink&amp;gt;&amp;lt;/jmol&amp;gt; are ...&lt;br /&gt;
&lt;br /&gt;
==Tour of things not shown in the physical model==&lt;br /&gt;
&lt;br /&gt;
===Substrate binding===&lt;br /&gt;
&amp;lt;scene name=&#039;78/785360/Substrate/1&#039;&amp;gt;&lt;br /&gt;
Substrate binding&amp;lt;/scene&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Shape of the protein===&lt;br /&gt;
&amp;lt;jmol&amp;gt;&amp;lt;jmolLink&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;  select protein; isosurface ignore (not selected) SASURFACE 1.2&lt;br /&gt;
  &amp;lt;/script&amp;gt;&lt;br /&gt;
  &amp;lt;text&amp;gt;molecular surface&amp;lt;/text&amp;gt;&lt;br /&gt;
&amp;lt;/jmolLink&amp;gt;&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Active site residues===&lt;br /&gt;
&amp;lt;scene name=&#039;78/785360/Acidbase/1&#039;&amp;gt;Active site residues&amp;lt;/scene&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Hydrophobic core===&lt;br /&gt;
&amp;lt;scene name=&#039;78/785360/Core/1&#039;&amp;gt;Hydrophobic core&amp;lt;/scene&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;scene name=&#039;78/785360/Physmodel/1&#039;&amp;gt;Back to overall view&amp;lt;/scene&amp;gt;&lt;br /&gt;
&lt;br /&gt;
== Function ==&lt;br /&gt;
&lt;br /&gt;
== Disease ==&lt;br /&gt;
&lt;br /&gt;
== Relevance ==&lt;br /&gt;
&lt;br /&gt;
== Structural highlights ==&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=User:Jaime_Prilusky/Test/MSOE&amp;diff=4395862</id>
		<title>User:Jaime Prilusky/Test/MSOE</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=User:Jaime_Prilusky/Test/MSOE&amp;diff=4395862"/>
		<updated>2025-11-28T14:50:12Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==A SMART Team Projet from Brown Deer High School==&lt;br /&gt;
&amp;lt;StructureSection load=&#039;3rec&#039; size=&#039;350&#039; side=&#039;right&#039; caption=&#039;The physical model was designed using Jmol&#039; scene=&#039;78/784319/Browndeerhs_2016-17/3&#039;&amp;gt;&lt;br /&gt;
SMART Teams (Students Modeling a Research Topic) is a student outreach program run by the [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling], in which students work with a researcher to create 3D printed physical models of a protein structure. Below is a summary of the 2016-17 Brown Deer High School SMART Team project, focused on the potassium channel protein.&lt;br /&gt;
&lt;br /&gt;
[[Image:SmartTeams_brownDeerHS_2016-17_poster.jpg | 550px]]&lt;br /&gt;
[[Image:SmartTeams_brownDeerHS_2016-17_model.jpg | 450px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
====The MSOE Center for BioMolecular Modeling====&lt;br /&gt;
[[Image:CbmUniversityLogo.jpg | left | 150px]]&lt;br /&gt;
The [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling] uses 3D printing technology to create physical models of protein and molecular structures, making the invisible molecular world more tangible and comprehensible. To view more protein structure models, visit our [http://cbm.msoe.edu/educationalmedia/modelgallery/ Model Gallery].&lt;br /&gt;
&lt;br /&gt;
 [[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Cystic_fibrosis_transmembrane_conductance_regulator_(CFTR)&amp;diff=4395861</id>
		<title>Cystic fibrosis transmembrane conductance regulator (CFTR)</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Cystic_fibrosis_transmembrane_conductance_regulator_(CFTR)&amp;diff=4395861"/>
		<updated>2025-11-28T14:48:10Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Cystic fibrosis transmembrane conductance regulator (CFTR)==&lt;br /&gt;
&amp;lt;StructureSection load=&#039;5UAK&#039; size=&#039;340&#039; side=&#039;right&#039; caption=&#039;Cystic Fibrosis Transmembrane Conductance regulator&#039; scene=&#039;&#039;&amp;gt;&lt;br /&gt;
The &#039;&#039;&#039;CFTR&#039;&#039;&#039; is a chloride channel, and is regulated by PKA phosphorylation, cAMP levels, and ATP/ADP ratios.  Mutations in the CFTR cause the disease cystic fibrosis.&lt;br /&gt;
&lt;br /&gt;
CFTR is a mostly &amp;lt;scene name=&#039;78/785332/Secondary_structure/1&#039;&amp;gt;alpha helical&amp;lt;/scene&amp;gt;  protein.  The membrane spanning segments can be clearly seen with coloring by &amp;lt;scene name=&#039;78/785332/Hydrophobicity/1&#039;&amp;gt;hydrophobicity&amp;lt;/scene&amp;gt;, which shows hydrophobic residues in gray and hydrophilic residues in purple.&lt;br /&gt;
&lt;br /&gt;
The extracellular end of the channel has several &amp;lt;scene name=&#039;78/785332/Ec_cl_selection/1&#039;&amp;gt;positively charged&amp;lt;/scene&amp;gt; residues that are important for recruiting chloride ions to the channel. A number of &amp;lt;scene name=&#039;78/785332/Plus_channel/1&#039;&amp;gt;positively charged&amp;lt;/scene&amp;gt; residues line the channel. In the unphosphorylated state (as this structure is), a &amp;lt;scene name=&#039;78/785332/Regulatory_domain/2&#039;&amp;gt;regulatory domain&amp;lt;/scene&amp;gt;  blocks the activity of the channel (the connecting segments are not visible in the structure).  It contains several negatively charged residues; when the protein is phosphorylated, this segment is repelled, causing a structural change. &amp;lt;ref&amp;gt;PMID:28340353&amp;lt;/ref&amp;gt; In the unphosphorylated state, P99,G103,R104,R334,K335,F337,N1138 &amp;lt;scene name=&#039;78/785332/Blocked_channel/1&#039;&amp;gt;block the channel&amp;lt;/scene&amp;gt;; in the &amp;lt;scene name=&#039;78/785332/Phosphorylated_pore/1&#039;&amp;gt;phosphorylated state&amp;lt;/scene&amp;gt;, these amino acids are moved out of the way, creating a pore large enough for a chloride ion to move through the channel.&lt;br /&gt;
&lt;br /&gt;
CFTR contains two &amp;lt;scene name=&#039;78/785332/Nbd/2&#039;&amp;gt;nucleotide binding domains&amp;lt;/scene&amp;gt; (NBD&#039;s), which both contain &amp;lt;scene name=&#039;78/785332/Walker_motifs/2&#039;&amp;gt;Walker motifs&amp;lt;/scene&amp;gt;, flexible loops that bind phosphate groups tightly and are highly conserved among ATP-binding proteins. &lt;br /&gt;
&lt;br /&gt;
==Mutations in Cystic Fibrosis==&lt;br /&gt;
&lt;br /&gt;
Cystic fibrosis is characterized by decreased chloride transport, which causes mucus to be thicker and stickier. This leads to a variety of problems, including decreased lung capacity, decreased pancreatic enzyme release into the small intestine, increased rates of lung infections, and infertility.&amp;lt;ref&amp;gt;https://ghr.nlm.nih.gov/condition/cystic-fibrosis&amp;lt;/ref&amp;gt;  There are a wide assortment of mutations that cause cystic fibrosis, with differing symptom severity.  The deletion of &amp;lt;scene name=&#039;78/785332/F508/1&#039;&amp;gt;F508&amp;lt;/scene&amp;gt; causes the protein to not be properly synthesized, and no expression is seen on the cell surface. Other mutations are found in the NBD&#039;s; some of these mutations such as S1255P alter the responsiveness to MgATP, while others such as G551S, G1244E, and G1239D decrease the frequency of channel opening.&lt;br /&gt;
&lt;br /&gt;
Some of the mutations that lead to cystic fibrosis are due to folding errors.  There are &amp;lt;scene name=&#039;78/785332/Numbered_bundles/2&#039;&amp;gt;12 transmembrane sequences&amp;lt;/scene&amp;gt; in CFTR; they are not sequential in their packing.  The presence of &amp;lt;scene name=&#039;78/785332/Numbered_bundles_pos_res/1&#039;&amp;gt;hydrophilic, positively charged amino acids&amp;lt;/scene&amp;gt; in these transmembrane sequences (shown in red) lead to a folding problem: how do you stabilize them until they can be protected by hydrophobic residues and are no longer exposed to the hydrophobic membrane?&lt;br /&gt;
&lt;br /&gt;
==3D Printed Physical Model of the CFTR protein==&lt;br /&gt;
&lt;br /&gt;
Shown below are 3D printed physical models of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein. The backbone model on the left is colored by region, with the transmembrane domain white and the atp-binding and regulatory domains colored red.  The backbone model on the right is colored by regional repeat, with the first repeat blue, the second repeat green and the regulatory domain colored red.  The models have been designed with embedded magnets to disassemble into the key regions of the structure.&lt;br /&gt;
&lt;br /&gt;
[[Image:cftr1_centerForBioMolecularModeling.jpg|500px]]&lt;br /&gt;
[[Image:cftr2_centerForBioMolecularModeling.jpg|500px]]&lt;br /&gt;
&lt;br /&gt;
====The MSOE Center for BioMolecular Modeling====&lt;br /&gt;
&lt;br /&gt;
[[Image:CbmUniversityLogo.jpg | left | 150px]]&lt;br /&gt;
&lt;br /&gt;
The [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling] uses 3D printing technology to create physical models of protein and molecular structures, making the invisible molecular world more tangible and comprehensible. To view more protein structure models, visit our [http://cbm.msoe.edu/educationalmedia/modelgallery/ Model Gallery].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
 [[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=User:Mark_Hoelzer/Sandbox2&amp;diff=4395860</id>
		<title>User:Mark Hoelzer/Sandbox2</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=User:Mark_Hoelzer/Sandbox2&amp;diff=4395860"/>
		<updated>2025-11-28T14:46:51Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==NMDAR Helps You Think, So Please Reconsider That Extra Drink==&lt;br /&gt;
====A SMART Team Projet from Brown Deer High School====&lt;br /&gt;
&lt;br /&gt;
SMART Teams (Students Modeling a Research Topic) is a student outreach program run by the [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling], in which students work with a researcher to create 3D printed physical models of a protein structure. Below is a summary of the 2016-17 Brown Deer High School SMART Team project, focused on the potassium channel protein.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;4pe5&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;The physical model was designed using Jmol&#039; scene=&#039;78/784319/Browndeerhs_2016-17/3&#039; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:SmartTeams_brownDeerHS_2016-17_poster.jpg | 550px]]&lt;br /&gt;
[[Image:SmartTeams_brownDeerHS_2016-17_model.jpg | 450px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
====The MSOE Center for BioMolecular Modeling====&lt;br /&gt;
&lt;br /&gt;
[[Image:CbmUniversityLogo.jpg | left | 150px]]&lt;br /&gt;
&lt;br /&gt;
The [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling] uses 3D printing technology to create physical models of protein and molecular structures, making the invisible molecular world more tangible and comprehensible. To view more protein structure models, visit our [http://cbm.msoe.edu/educationalmedia/modelgallery/ Model Gallery].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=User:Karsten_Theis/Physical_Models&amp;diff=4395859</id>
		<title>User:Karsten Theis/Physical Models</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=User:Karsten_Theis/Physical_Models&amp;diff=4395859"/>
		<updated>2025-11-28T14:45:10Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==3D printed models==&lt;br /&gt;
&lt;br /&gt;
Using a 3D printer from Westfield State University, we printed physcial models of proteins illustrating concepts such as chirality, shape complementarity of binding sites and ligand, protein flexibility, misfolding, protein aggregation and protein stability aided by disulfide bonds.&lt;br /&gt;
&lt;br /&gt;
We have started to create a proteopedia article, along with video footage, for each of the available models. This is work in progress, so all of the pages are still in the sandbox stage. Nevertheless, here are links to each of them:&lt;br /&gt;
&lt;br /&gt;
*Antibodies: [[User:LeeAnne Brown/Sandbox 1]]&lt;br /&gt;
*Amyloid beta fibrils:[[User:Kaeleigh Chartrand/SANDBOX]]&lt;br /&gt;
*Sickle cell hemoglobin: [[Eric Comeau/ sandbox]]&lt;br /&gt;
*Ibuprofen binds to cyclooxygenase:[[User:Nicholas P. Taliceo/Sandbox]]&lt;br /&gt;
*Salbultamol: [[Emily Ellis/Sandbox]]&lt;br /&gt;
*Insulin: [[Heather Kirby-sandbox]]&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Anthrax_Toxin_Protein&amp;diff=4395858</id>
		<title>Anthrax Toxin Protein</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Anthrax_Toxin_Protein&amp;diff=4395858"/>
		<updated>2025-11-28T14:29:49Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;StructureSection load=&#039;1acc&#039; size=&#039;350&#039; side=&#039;right&#039; caption=&#039;Anthrax protective antigen (PA83) complex with Ca+2 ions (PDB code [[1acc]])&#039; scene=&#039;&#039;&amp;gt;&lt;br /&gt;
==3D Printed Physical Models of the Anthrax Toxin Protein==&lt;br /&gt;
&lt;br /&gt;
Shown below are 3D printed physical models of the Anthrax Toxin Protein, based on the structure [http://proteopedia.org/wiki/index.php/1acc 1acc.pdb]. The full heptamer model is shown in spacefill format and is colored by domain, with a single monomer shown in white. The alpha carbon backbone model is similarly colored by chain, with additional key sidechains included.&lt;br /&gt;
&lt;br /&gt;
[[Image:anthrax_1_centerForBiomolecularModeling.jpg | 500px]] &lt;br /&gt;
[[Image:anthrax_2_centerForBiomolecularModeling.jpg | 500px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
====The MSOE Center for BioMolecular Modeling====&lt;br /&gt;
&lt;br /&gt;
[[Image:CbmUniversityLogo.jpg | left | 100px]]&lt;br /&gt;
&lt;br /&gt;
The [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling] uses 3D printing technology to create physical models of protein and molecular structures, making the invisible molecular world more tangible and comprehensible. To view more protein structure models, visit our [http://cbm.msoe.edu/educationalmedia/modelgallery/ Model Gallery].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
This is a sample scene created with SAT to &amp;lt;scene name=&amp;quot;/12/3456/Sample/1&amp;quot;&amp;gt;color&amp;lt;/scene&amp;gt; by Group, and another to make &amp;lt;scene name=&amp;quot;/12/3456/Sample/2&amp;quot;&amp;gt;a transparent representation&amp;lt;/scene&amp;gt; of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=ATPase&amp;diff=4395857</id>
		<title>ATPase</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=ATPase&amp;diff=4395857"/>
		<updated>2025-11-28T14:29:32Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;StructureSection load=&#039;RuvBL12_12mer.pdb&#039; size=&#039;400&#039; side=&#039;right&#039; scene=&#039;Journal:JSB:1/Cv/2&#039; caption=&#039;An ATPase, Human RuvB-like 1 dodecamer complex with ADP (PDB code [[2c9o]])&#039;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[ATPase]] is an enzyme which catalyzes the breakdown of [[ATP]] into ADP and a phosphate ion.  This dephosphorylation releases energy which the enzyme uses to drive other reactions&amp;lt;ref&amp;gt;PMID:15078220&amp;lt;/ref&amp;gt;. The F1/0 ATPase is called &#039;&#039;&#039;ATP synthase&#039;&#039;&#039; synthesises the reverse reaction, i.e., the addition of phosphate to ADP to form ATP&amp;lt;ref&amp;gt;PMID:30888962&amp;lt;/ref&amp;gt;.  ATPase types include:&amp;lt;br /&amp;gt;&lt;br /&gt;
* &#039;&#039;&#039;F-ATPase&#039;&#039;&#039; - the prime producers of ATP&amp;lt;ref&amp;gt;PMID:8065448&amp;lt;/ref&amp;gt;.  For details see [[Alice Clark/ATPsynthase]];&amp;lt;br /&amp;gt; &amp;lt;!--Should there be a F-ATPase page for this like thee is for V-ATPase below? If one is made, I&#039;d like to see links to the animations/movies referenced at https://twitter.com/NathanRoberts17/status/943428752113094656 there.--&amp;gt;&lt;br /&gt;
* &#039;&#039;&#039;V-ATPase&#039;&#039;&#039; or Vacuolar-type H+ ATPase couples the energy to proton transport across membranes.  &lt;br /&gt;
&lt;br /&gt;
ATPase is inhibited by [[Bedaquiline]] which is used as TB drug&amp;lt;ref&amp;gt;PMID:28807917&amp;lt;/ref&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
For details see [[V-ATPase]];&amp;lt;br /&amp;gt;&lt;br /&gt;
* &#039;&#039;&#039;A-ATPase&#039;&#039;&#039; are found in archaea.  For details see [[A-ATP Synthase]];&amp;lt;br /&amp;gt;&lt;br /&gt;
* &#039;&#039;&#039;P-ATPase&#039;&#039;&#039; transport ions&amp;lt;ref&amp;gt;PMID:20962537&amp;lt;/ref&amp;gt;&amp;lt;br /&amp;gt;&lt;br /&gt;
* &#039;&#039;&#039;E-ATPase&#039;&#039;&#039; hydrolyze extracellular ATP&amp;lt;ref&amp;gt;PMID:7721538&amp;lt;/ref&amp;gt;.  &amp;lt;br /&amp;gt;&lt;br /&gt;
*  &#039;&#039;&#039;MipZ&#039;&#039;&#039; is an ATPase which forms a complex with the chromosome partitioning protein ParB and is responsible for the regulation of FtsZ ring formation.&amp;lt;br /&amp;gt;&lt;br /&gt;
ATPase domains include metal-binding domain (MBD) and nucleotide-binding domain (NBD). For more details see:&amp;lt;br /&amp;gt;&lt;br /&gt;
* &#039;&#039;&#039;ATPase RavA&#039;&#039;&#039; participates in the pathway which response to ahminoglycosides under anaerobic conditions and cell membrane regulation&amp;lt;ref&amp;gt;PMID:36127320&amp;lt;/ref&amp;gt;.  &amp;lt;br /&amp;gt;&lt;br /&gt;
* &#039;&#039;&#039;ATPase InvC&#039;&#039;&#039; energizes the apparatus needed for the entry of &#039;&#039;Salmonella typhimurium&#039;&#039; into mammalian cells&amp;lt;ref&amp;gt;PMID:8045880&amp;lt;/ref&amp;gt;.  &amp;lt;br /&amp;gt;&lt;br /&gt;
* &#039;&#039;&#039;Peroxisomal ATPase&#039;&#039;&#039; Pex1/Pex6 is essential for peroxisome formation&amp;lt;ref&amp;gt;PMID:37741838&amp;lt;/ref&amp;gt;.  &amp;lt;br /&amp;gt;&lt;br /&gt;
* &#039;&#039;&#039;INO8o ATPase&#039;&#039;&#039; is a component of the chromatin remodelling complex&amp;lt;ref&amp;gt;PMID:19062292&amp;lt;/ref&amp;gt;.  &amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;Cu transporting ATPase&#039;&#039;&#039; are in [[P(1B)-Type Cu(I) Transporting ATPases ATP7A and ATP7B]].&amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;Na/K transporting ATPase&#039;&#039;&#039; are in [[Sodium-Potassium ATPase]].&amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;H/K transporting ATPase&#039;&#039;&#039; are in [[Esomeprazole and H+/K+ - ATPase Interaction]].&amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;Transitional endoplasmic reticulum ATPase&#039;&#039;&#039; are in [[Valosin Containing Protein D120]].&amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;Central stalk in F(1)-ATPase&#039;&#039;&#039; is described in [[A-ATP Synthase]]&amp;lt;br /&amp;gt;&lt;br /&gt;
*[[Journal:JSB:1|RuvBL1/RuvBL2 complex (ATPase)]]&amp;lt;br /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==3D Printed Physical Model of ATP Synthase==&lt;br /&gt;
&lt;br /&gt;
Shown below is a 3D printed physical model of the Respiration Electron Transport Chain. Complex I is colored red, complex II is purple, complex III is green, complex IV is blue and the atp synthase protein is colored orange, yellow and red.&lt;br /&gt;
[[Image:atpSynthase1_centerForBioMolecularModeling.jpg |550px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
====The MSOE Center for BioMolecular Modeling====&lt;br /&gt;
&lt;br /&gt;
[[Image:CbmUniversityLogo.jpg | left | 150px]]&lt;br /&gt;
&lt;br /&gt;
The [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling] uses 3D printing technology to create physical models of protein and molecular structures, making the invisible molecular world more tangible and comprehensible. To view more protein structure models, visit our [http://cbm.msoe.edu/educationalmedia/modelgallery/ Model Gallery].&lt;br /&gt;
&lt;br /&gt;
== 3D Structures of ATPase ==&lt;br /&gt;
[[ATPase 3D structures]]&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:Topic Page]]&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Fibrinogen&amp;diff=4395856</id>
		<title>Fibrinogen</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Fibrinogen&amp;diff=4395856"/>
		<updated>2025-11-28T14:29:07Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;StructureSection load=&#039;1n73&#039; size=&#039;350&#039; side=&#039;right&#039; scene=&#039;41/410324/Cv/1&#039; caption=&#039;Crystal structure of glycosylated fibrinogen fragment D.  Subunit α (green and yellow), β (green and magenta), γ (pink and cyan) complex with the peptide ligand Gly-His-Arg-Pro-amide (red, wheat, blue, black) and Ca+2 ion (PDB code [[1n73]]) &#039;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
== Function ==&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Fibrinogen&#039;&#039;&#039; is a glycoprotein found in the blood that is converted into fibrin during blood coagulation. Fibrinogen is cleaved by another protein, [[thrombin]], exposing knobs A and B to form fibrin. &amp;lt;ref&amp;gt;PMID:16689770&amp;lt;/ref&amp;gt; The fibrin forms clots to prevent excessive bleeding from wounds sustained. Clotting factors, like factor XIII, are often linked to fibrin. &amp;lt;ref&amp;gt;PMID:18673233&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==3D Printed Physical Model of Fibrinogen==&lt;br /&gt;
&lt;br /&gt;
Shown below is a 3D printed physical model of Fibrinogen. The structure is shown as an alpha carbon backbone colored by chain, with the three chains of each copy of fibrinogen colored yellow, blue and purple.&lt;br /&gt;
&lt;br /&gt;
[[Image:fibrinogen1_centerForBioMolecularModeling.jpg|550px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
====The MSOE Center for BioMolecular Modeling====&lt;br /&gt;
&lt;br /&gt;
[[Image:CbmUniversityLogo.jpg | left | 150px]]&lt;br /&gt;
&lt;br /&gt;
The [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling] uses 3D printing technology to create physical models of protein and molecular structures, making the invisible molecular world more tangible and comprehensible. To view more protein structure models, visit our [http://cbm.msoe.edu/educationalmedia/modelgallery/ Model Gallery].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Structural insights ==&lt;br /&gt;
&lt;br /&gt;
Fibrinogen is composed of 2 copies each of 3 non-identical chains α, β, γ (&amp;lt;scene name=&#039;Fibrinogen/Fba/1&#039;&amp;gt;Fba&amp;lt;/scene&amp;gt;, &amp;lt;scene name=&#039;Fibrinogen/Fbb/1&#039;&amp;gt;Fbb&amp;lt;/scene&amp;gt;, &amp;lt;scene name=&#039;Fibrinogen/Fbg/1&#039;&amp;gt;Fbg&amp;lt;/scene&amp;gt;).  &lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==3D Structure of Fibrinogen==&lt;br /&gt;
&lt;br /&gt;
Updated on {{REVISIONDAY2}}-{{MONTHNAME|{{REVISIONMONTH}}}}-{{REVISIONYEAR}}&lt;br /&gt;
{{#tree:id=OrganizedByTopic|openlevels=0|&lt;br /&gt;
&lt;br /&gt;
*Fibrinogen α+β+γ chains&lt;br /&gt;
&lt;br /&gt;
**[[3hus]], [[3h32]], [[3e1i]], [[3bvh]], [[2hlo]], [[2hod]], [[2hpc]], [[2oyh]], [[2oyi]], [[2h43]], [[2ffd]], [[1re3]], [[1rf1]], [[1n86]], [[1ltj]] – hFba+hFbb+hFbg+peptide ligand – human&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[3ghg]], [[2q9i]], [[2z4e]] - hFba+hFbb+hFbg+knob A &amp;amp; B&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[2xnx]], [[2xny]] - hFba+hFbb+hFbg + M1 protein&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[2a45]] - hFba+hFbb+hFbg+thrombin+PPACK thrombin inhibitor&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[1re4]], [[1rf0]], [[1n8e]], [[1lt9]] - hFba+hFbb+hFbg&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[1jy3]], [[1deq]] – bFba+Fbb+Fbg – bovine&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[1jy2]] - bFba+Fbb+Fbg proteolytic fragment&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[1m1j]] - cFba+Fbb+Fbg+peptide ligand – chicken&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[1ei3]] - cFba+Fbb+Fbg&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[1n73]], [[1lwu]] - Fba+Fbb+Fbg+peptide ligand – Sea lamprey&amp;lt;br /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
*Fibrinogen α chain&lt;br /&gt;
&lt;br /&gt;
**[[1fzd]] – hFba EC domain&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[1bbr]] – hFba+cε-thrombin&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[2jor]] – bFba – NMR&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[2baf]] – bFba&amp;lt;br /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
*Fibrinogen β chain&lt;br /&gt;
&lt;br /&gt;
**[[1fzf]], [[1fzg]] – hFb fragment double-D +peptide ligand&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[1fze]], [[1fza]], [[1fzb]] – hFb fragment D&amp;lt;br /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
*Fibrinogen γ chain&lt;br /&gt;
&lt;br /&gt;
**[[1fic]], [[1fid]] – hFbg&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[3fib]] – hFbg C terminal&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[2vr3]] – hFbg+SaClumping Factor A – &#039;&#039;Staphylococcus aureus&#039;&#039;&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[2vdo]], [[2vdp]], [[2vdq]], [[2vdr]] – hFbg+Integrin alpha IIB+Integrin beta-3+ antibody &amp;lt;br /&amp;gt;&lt;br /&gt;
**[[2fib]], [[3fib]] - hFbg+peptide ligand&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[1fib]] – hFbg+Ca&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[2hwl]] – hFbg peptide+prothrombin&amp;lt;br /&amp;gt;&lt;br /&gt;
**[[2y7l]] – hFbg + agglutinin-like protein &amp;lt;br /&amp;gt;&lt;br /&gt;
**[[1dug]] – Fbg C-terminal/glutathione S-transferase – &#039;&#039;Schistosoma japonicum&#039;&#039;&amp;lt;br /&amp;gt;&lt;br /&gt;
}}&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:Topic Page]]&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Hemolysin&amp;diff=4395855</id>
		<title>Hemolysin</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Hemolysin&amp;diff=4395855"/>
		<updated>2025-11-28T14:28:36Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;StructureSection load=&#039;7ahl&#039; size=&#039;350&#039; side=&#039;right&#039; caption=&#039;α-hemolysin heptamer (PDB code [[7ahl]]).&#039; scene=&#039;&#039;&amp;gt;&lt;br /&gt;
== Function ==&lt;br /&gt;
&#039;&#039;&#039;Hemolysin&#039;&#039;&#039; (HL) is exotoxin from bacteria which causes lysis of red blood cells&amp;lt;ref&amp;gt;PMID:20110774&amp;lt;/ref&amp;gt;. &lt;br /&gt;
*&#039;&#039;&#039;alpha-hemolysin&#039;&#039;&#039; is a transmembrane pore-forming heptameric molecule&amp;lt;ref&amp;gt;PMID:8943190&amp;lt;/ref&amp;gt;.  See details for in [[Pore forming toxin, α-hemolysin]].  &lt;br /&gt;
*&#039;&#039;&#039;delta-hemolysin&#039;&#039;&#039; is a 26 amino acid peptide from the bacterium &#039;&#039;Staphylococcus&#039;&#039; exhibiting antimicrobial activity against&#039;&#039; Legionerlla&#039;&#039; &amp;lt;ref&amp;gt;PMID:19150639&amp;lt;/ref&amp;gt;. &lt;br /&gt;
&lt;br /&gt;
See details of hemolysin E in [[Molecular Playground/ClyA]].&lt;br /&gt;
&lt;br /&gt;
For toxins in Proteopdia see [[Toxins]].&lt;br /&gt;
&lt;br /&gt;
== Relevance ==&lt;br /&gt;
HL acts as a virulence factor in the pathogenesis of invasive infections&amp;lt;ref&amp;gt;PMID:12564994&amp;lt;/ref&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==3D Printed Physical Model of Hemolysin==&lt;br /&gt;
&lt;br /&gt;
Shown below is a 3D printed physical model of Hemolysin. The model is shown in alpha carbon backbone format with each chain colored uniquely. &lt;br /&gt;
&lt;br /&gt;
[[Image:hemolysin1_centerForBioMolecularModeling.jpg|550px]]&lt;br /&gt;
[[Image:hemolysin2_centerForBioMolecularModeling.jpg|550px]]&lt;br /&gt;
&lt;br /&gt;
====The MSOE Center for BioMolecular Modeling====&lt;br /&gt;
&lt;br /&gt;
[[Image:CbmUniversityLogo.jpg | left | 150px]]&lt;br /&gt;
&lt;br /&gt;
The [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling] uses 3D printing technology to create physical models of protein and molecular structures, making the invisible molecular world more tangible and comprehensible. To view more protein structure models, visit our [http://cbm.msoe.edu/educationalmedia/modelgallery/ Model Gallery].&lt;br /&gt;
&lt;br /&gt;
== 3D Structures of hemolysin ==&lt;br /&gt;
&lt;br /&gt;
[[Hemolysin 3D structures]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
[[Category:Topic Page]]&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Hemagglutinin&amp;diff=4395854</id>
		<title>Hemagglutinin</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Hemagglutinin&amp;diff=4395854"/>
		<updated>2025-11-28T14:28:05Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;StructureSection load=&#039;&#039; size=&#039;350&#039; side=&#039;right&#039; scene =&#039;Hemagglutinin/Blackground2wre/1&#039; caption=&#039;Structure of glycosylated viral hemagglutinin trimer complex with galactose ([[2wre]])&#039;&amp;gt;&lt;br /&gt;
== Function ==&lt;br /&gt;
[[Hemagglutinin|Hemagglutinins]] (HA) are one of the two antigenic Glycoproteins inserted into the influenza virus&#039; membrane. There are at least 16 different forms of HA antigens classified from H1 to H16. H1, H2, H3 are specific to human [[influenza]]. HAs have two main functions crucial for the [[Viral Infections|viral infection]] cycle:&lt;br /&gt;
1. On the target cell, HA binds the receptor on the cell membrane which is contains sialic acid &amp;lt;ref&amp;gt;Gottschalk A. Chemistry of virus receptors. The Viruses. 1959;3:51–61.&amp;lt;/ref&amp;gt; allowing the virus/cell interaction.&lt;br /&gt;
2. HA induce the fusion between the host cell and the virus which can entry into the cytoplasm.&lt;br /&gt;
Because the HA are the major Antigens of the Virus, [[Antibody|Antibodies]] recognized them and for this reason HA often change. &lt;br /&gt;
* &#039;&#039;&#039;Dr hemagglutinin&#039;&#039;&#039; is found in urinary tract pathogenic &#039;&#039;E. coli&#039;&#039; and recognizes Dr blood group antigen&amp;lt;ref&amp;gt;PMID: 3054548&amp;lt;/ref&amp;gt;.&lt;br /&gt;
* &#039;&#039;&#039;Phytohemagglutinin&#039;&#039;&#039; is found in bean seeds and has sugar binding and hemagglutinin functions&amp;lt;ref&amp;gt;PMID: 8702788&amp;lt;/ref&amp;gt;.&lt;br /&gt;
* &#039;&#039;&#039;Hemagglutinin-neuraminidase&#039;&#039;&#039; (HN) is multifunctional.  It possesses both the receptor recognition and neuraminidase activities&amp;lt;ref&amp;gt;PMID:21680512&amp;lt;/ref&amp;gt;.  For details see [[Mumps Virus Hemagglutinin Neuraminidase Protein]].&lt;br /&gt;
&lt;br /&gt;
For discussion of influenza hemagglutinin see&amp;lt;br /&amp;gt;&lt;br /&gt;
*[[Influenza hemagglutinin]]&amp;lt;br /&amp;gt;&lt;br /&gt;
*[[Influenza]]&amp;lt;br /&amp;gt;&lt;br /&gt;
*[[User:Michael Strong/H1N1/HA]]&amp;lt;br /&amp;gt;&lt;br /&gt;
*[[User:Michael Strong/H1N1/HA/MSA]] for multiple sequence alignment.&lt;br /&gt;
&lt;br /&gt;
==Hemagglutinin Structure==&lt;br /&gt;
HA is an &amp;lt;scene name=&#039;Hemagglutinin/Homotrimer/2&#039;&amp;gt;homotrimer&amp;lt;/scene&amp;gt; integral membrane glycoprotein. Each monomer is synthesized like a single polypeptide chain almost 550 amino acids. This precursor is then glycosilated and cleaved into two smaller polypeptides by removal of Arginine 329; at the same time, a conformational change occurs in the monomer. &lt;br /&gt;
&lt;br /&gt;
The HA1 and HA2 subunits are covalently attached by a &amp;lt;scene name=&#039;SAndbox_159/Disulfide_bond/2&#039;&amp;gt;disulfide bond&amp;lt;/scene&amp;gt; from HA1 position 14 to HA2 position 467(*). These two chains form one monomer, and the noncovalentely association of three monomers forms one hemagglutinin molecule: (HA1+HA2)3. It is principally stabilized by packing of the alpha-helixes. All molecules are 135 Angström long.&lt;br /&gt;
&lt;br /&gt;
The &amp;lt;scene name=&#039;SAndbox_159/Ha1/1&#039;&amp;gt;HA1 subunit&amp;lt;/scene&amp;gt; (328 amino acids) has a globular form outside the virus’ membrane: it is composed by an eight-stranded beta-sheet, associated with a little alpha-helix, separating the strands 3 and 4. &lt;br /&gt;
The amino acids of this alpha-helix, and some others around it, included in the beta-sheet, compose the binding site for the receptor’s sialic acid. Thus, for one molecule of hemagglutinin, there are three binding sites to the host cell’s receptor.&lt;br /&gt;
&lt;br /&gt;
The &amp;lt;scene name=&#039;SAndbox_159/Ha2/2&#039;&amp;gt;HA2 subunit&amp;lt;/scene&amp;gt; (221 amino acids) has a hair spin structure composed by two antiparallel alpha-helixes. One of these belongs to the longest alpha-helixes in globular protein: it is 50 angstrom long. The hydrophobic N-terminus part of HA2, called fusion peptide, is close to a protease’s cleavage site: this protease is implied in the virus’ entry in the host cell.&lt;br /&gt;
&lt;br /&gt;
HA1 and HA2 are bound each other by a disulfide bind. The three long alpha-helixes (of the three HA2) are coiled-coil to form a central region of 40 Angström, and thank to the hydrophobic amino acids and those which form salt bridges bound, we obtain a HA stabilized.&amp;lt;ref&amp;gt;PMID: 3304138&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==2WRE==&lt;br /&gt;
&lt;br /&gt;
To begin, this code corresponds to the structure of influenza H2 Avian Hemagglutinin from the “Asian Influenza” of 1957.&amp;lt;ref&amp;gt;PMID :19805083&amp;lt;/ref&amp;gt; Human receptor.&lt;br /&gt;
-	At the position 226, Avian Hemagglutinin has a Glutamine residue whereas the Human one has Leucine&lt;br /&gt;
&lt;br /&gt;
-	At the position 228, there is a Glycin for Avian HA whereas a Serine for Human HA.&lt;br /&gt;
&lt;br /&gt;
These two mutations prevent the human H2 binding on the avian receptor whereas the human receptor can be bound by avian hemagglutinin that lacks the human specific mutation of H2 pandemic viruses.&lt;br /&gt;
&lt;br /&gt;
There are three sites for sialic acid binding, which are at the membrane-distal tips of the identical monomers that form the HA trimer:&lt;br /&gt;
&lt;br /&gt;
-   The first one is the &amp;lt;scene name=&#039;SAndbox_159/Loop_220/2&#039;&amp;gt;Loop 220&amp;lt;/scene&amp;gt; composed by the residues from 225 to 228&lt;br /&gt;
&lt;br /&gt;
-   The second is called &amp;lt;scene name=&#039;SAndbox_159/Loop_130/1&#039;&amp;gt;Loop 130&amp;lt;/scene&amp;gt; and contains the residues 131 to 137&lt;br /&gt;
&lt;br /&gt;
-   the last is named 190-helix&lt;br /&gt;
&lt;br /&gt;
[[Image:Avian.jpg|300px|thumb]]&lt;br /&gt;
{{Clear}}&lt;br /&gt;
The residues of these loops 130 and 220 have carbonyl oxygens and amide nitrogens of peptide bonds exposed with potential to interact with the receptor, which is composed by Gal-1 and Sia-2.&lt;br /&gt;
The avian H2 can bind the human receptor because of intramolecular Hydrogen bond network created by Gln 226 and by Asn 186. &lt;br /&gt;
Four amino acids compose &amp;lt;scene name=&#039;SAndbox_159/Receptor_binding_site/3&#039;&amp;gt;the receptor binding site&amp;lt;/scene&amp;gt;: Tyr 98, Ser 136, Trp 153(**), His 183, (which are identical in the all different HA)(*). This site forms a pocket on the distal end of the molecule. The binding structure is stabilized by other conserved which cannot interact with the receptor&lt;br /&gt;
&amp;lt;scene name=&#039;SAndbox_159/Amino_acids_in_the_stability/1&#039;&amp;gt;(Cys 97, Pro 99, Cis139, Pro 147, Tyr 195, Arg 229).&amp;lt;/scene&amp;gt;(*)  &lt;br /&gt;
The Sia-1-Gal-2 glycosidic bond adopts a cis conformation. Extensive hydrogen bond direction are settled between avian and Gal-2 of the receptor: two water molecules (Wat-1 and Wat-2) have a significant role in mediating these interactions(see fig.1).&lt;br /&gt;
The site chain of Lys-222 and the main chain carbonyl at 225 are linked by Wat-1 to the 3&#039;OH of Gal-2. Gln-226 and Asn 186 form hydrogen bonds with the hydroxyl groups of 4&#039;C of Gal-2 and 9&#039;C of Sia-1.&amp;lt;ref&amp;gt;Cell Binding protein in Avian Influenza; Jack Cerchiara,&#039;06 and Brendan Holsberry, 07;http://biology.kenyon.edu/BMB/Chime2/2005/Cerchiara-Holsberry/FRAMES/start.htm&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Oligosaccharides==&lt;br /&gt;
&lt;br /&gt;
Some &amp;lt;scene name=&#039;SAndbox_159/Asparagines/1&#039;&amp;gt;Asparagines&amp;lt;/scene&amp;gt; of HA1 (8, 22, 38, 81, 165, 285)(*) have oligosaccharides chains attached to them. The seventh oligasaccharide is linked to an Aspargine of HA2 (484). All of them are complex oligosaccharides and are on the lateral surfaces of the molecule, except for site and 165. No precise functions have been assigned to them, even if the oligosaccharide at 165 seems to allow the stabilisation of oligomeric contact between globular units at the top of the protein&#039;s structure. &lt;br /&gt;
&lt;br /&gt;
==Antigenic variability==&lt;br /&gt;
&lt;br /&gt;
Each Hemagglutinin monomer contains four antigenic sites called &amp;lt;scene name=&#039;SAndbox_159/Antigenic_site/1&#039;&amp;gt;A,B,C and D sites&amp;lt;/scene&amp;gt;. &amp;quot;A&amp;quot;(in red) site is a loop that protrudes 8 Angström distally from the surface of the target membrane. &amp;quot;B&amp;quot;(in green) site is composed by the external amino acids of one alpha helix and several amino acids of the receptor binding site which contains the sialic acid. &amp;quot;C&amp;quot;(in blue) site is a 60 Angström bulge from the distal extremity of HA. To finish, &amp;quot;D&amp;quot;(in mangenta) site is located in two beta-sheet of the jelly roll of HA1 globular extremity.&lt;br /&gt;
&lt;br /&gt;
The substitutions of amino acids in these sites allow the influenza virus to escape from the immune system and to spread. Major changes in these antigenic regions can produce lethal influenza pandemics, like in 1957.&lt;br /&gt;
&lt;br /&gt;
==How Influenza Escapes Vaccines==&lt;br /&gt;
&lt;br /&gt;
Influenza hemagglutinin (&#039;&#039;e.g.&#039;&#039; [[1hgf]]) is a glycoprotein on the surface of [http://en.wikipedia.org/wiki/Influenza_virus influenza virus] particles that enables them to attach to and infect host cells. [[Antibody|Antibodies]] that bind to hemagglutinin are a major defense mechanism that prevent infection. The RNA genome of influenza is characterized by a high mutation rate. Mutations on the surface of hemagglutinin tend to be protective for the virus. They tend to be retained because they tend to reduce the binding strength, and hence the host defensive capability, of antibodies that recognize the un-mutated hemagglutinin&amp;lt;ref name=&amp;quot;skehel_review&amp;quot;&amp;gt;PMID: 16925526&amp;lt;/ref&amp;gt;. Influenza vaccines include hemagglutinins and they induce anti-hemagglutinin antibodies in vaccinated individuals. Often, however, by the time the vaccines can be designed, produced, and disseminated, mutant influenza viruses have arisen that can cause disease in vaccinated individuals&amp;lt;ref name=&amp;quot;fluwikipedia&amp;quot;&amp;gt;See [http://en.wikipedia.org/wiki/Influenza Influenza] in Wikipedia.&amp;lt;/ref&amp;gt;.&lt;br /&gt;
If you &#039;&#039;&#039;show&#039;&#039;&#039; the &#039;&#039;&#039;Evolutionary Conservation&#039;&#039;&#039; of the structure on this page (using the blue bars below the molecule), you will see highly variable surface amino acids. These represent sites of mutations that have been retained in wild strains of influenza because they improve virus survival&amp;lt;ref name=&amp;quot;skehel_review&amp;quot; /&amp;gt;. (Added by [[User:Eric Martz|Eric Martz]]).&lt;br /&gt;
&lt;br /&gt;
==Notes==&lt;br /&gt;
(*)These four amino-acids don&#039;t have the same numbering in the text and on the picture because there is a frame shift between the PDB and the Swissprot sequence numbering.&lt;br /&gt;
&lt;br /&gt;
(**) The amino acid 153 lacks for the A monomer chain.&lt;br /&gt;
&lt;br /&gt;
==3D structures of hemagglutinin==&lt;br /&gt;
[[Hemagglutinin 3D structures]]&lt;br /&gt;
&lt;br /&gt;
==3D Printed Physical Models of Hemagglutinin==&lt;br /&gt;
&lt;br /&gt;
Shown below are 3D printed physical models of Hemagglutinin. The model is shown as an alpha carbon backbone, with key sidechains and domains highlighted. It has been designed with precisely embedded magnets that allow the three chains to pull apart into individual pieces.&lt;br /&gt;
 &lt;br /&gt;
&lt;br /&gt;
[[Image:hemagglutinin_1_centerForBiomolecularModeling.jpg | 450px]][[Image:hemagglutinin_2_centerForBiomolecularModeling.jpg | 450px]]&lt;br /&gt;
&lt;br /&gt;
====The MSOE Center for BioMolecular Modeling====&lt;br /&gt;
&lt;br /&gt;
[[Image:CbmUniversityLogo.jpg | left | 100px]]&lt;br /&gt;
&lt;br /&gt;
The [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling] uses 3D printing technology to create physical models of protein and molecular structures, making the invisible molecular world more tangible and comprehensible. To view more protein structure models, visit our [http://cbm.msoe.edu/educationalmedia/modelgallery/ Model Gallery].&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Additional Resources==&lt;br /&gt;
For additional information, see: [[Influenza]]&lt;br /&gt;
&amp;lt;br /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category: Topic Page]]&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Influenza&amp;diff=4395853</id>
		<title>Influenza</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Influenza&amp;diff=4395853"/>
		<updated>2025-11-28T14:27:08Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Image:800px-H1N1_navbox.jpg|350px|right|thumb| Picture of the H1N1 Influenza Virus]]&lt;br /&gt;
&lt;br /&gt;
[[Influenza]], commonly known as the Flu, is caused by RNA viruses of the family Orthomyxoviridae and takes the life of nearly 500,000 people per year. &amp;lt;br /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Articles in Proteopedia concerning [[Influenza]] include:&lt;br /&gt;
{{#tree:id=IndexByTopic|openlevels=1|&lt;br /&gt;
* [[Avian Influenza Neuraminidase, Tamiflu and Relenza]]&lt;br /&gt;
* H1N1 Sequence Analyses&lt;br /&gt;
** [[User:Michael_Strong/H1N1|H1N1 Swine Flu Sequence Analysis]]&lt;br /&gt;
** [[User:Michael_Strong/H1N1/MP1/MSA|H1N1 Swine Flu Multiple Sequence Alignment]]&lt;br /&gt;
** [[User:Michael Strong/H1N1/MP2/MSA|H1N1 Sequence Alignment of MP2 Protein]]&lt;br /&gt;
** [[User:Michael_Strong/H1N1/PB2|H1N1 Sequence Alignment of PB2 Protein]]&lt;br /&gt;
** [[User:Michael_Strong/H1N1/PB1|H1N1 Sequence Alignment of PB1 Protein]]&lt;br /&gt;
** [[User:Michael_Strong/H1N1/NS2/MSA|H1N1 Sequence Alignment of NS2 Protein]]&lt;br /&gt;
** [[User:Michael_Strong/H1N1/PA|H1N1 Sequence Alignment of PA Protein]]&lt;br /&gt;
** [[User:Michael_Strong/H1N1/HA|H1N1 Sequence Alignment of HA Protein]]&lt;br /&gt;
** [[User:Michael_Strong/H1N1/NP|H1N1 Sequence Alignment of NP Protein]]&lt;br /&gt;
** [[User:Michael_Strong/H1N1/NA|H1N1 Sequence Alignment of NA Protein]]&lt;br /&gt;
** [[User:Michael_Strong/H1N1/MP|H1N1 Sequence Alignment of MP Protein]]&lt;br /&gt;
** [[User:Michael_Strong/H1N1/NS|H1N1 Sequence Alignment of NS Protein]]&lt;br /&gt;
* [[Hemagglutinin]]&lt;br /&gt;
* [[Influenza hemagglutinin]]&lt;br /&gt;
* [[Molecular_Playground/Influenza_A_M2_transmembrane_domain|Influenza A M2 Transmembrane Domain]]&lt;br /&gt;
* [[Proton Channels]] w/ morph of the M2 proton channel of influenza.&lt;br /&gt;
* [[Molecular Playground/Tamiflu|Tamiflu Interaction]]&lt;br /&gt;
* [[Molecular Playground/Relenza|Relenza Interaction]]&lt;br /&gt;
}}&lt;br /&gt;
&amp;lt;br /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
To view automatically seeded indices concerning [[Influenza]] See:&lt;br /&gt;
*[[:Category:Influenza|Influenza]]&lt;br /&gt;
*[[:Category:Influenza_a_virus|Influenza A Virus]]&lt;br /&gt;
*[[:Category:Influenza_protein|Influenza Proteins]]&lt;br /&gt;
*[[:Category:H1n1|H1N1]]&amp;lt;br /&amp;gt;&lt;br /&gt;
&amp;lt;br /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
To View FDA Approved Treatments for [[Influenza]] See: [[Pharmaceutical_Drugs#Treatments|Treatments]]&amp;lt;br/&amp;gt;&lt;br /&gt;
To view other Proteopedia pages about diseases &amp;amp; drug targets, See: [[Pharmaceutical_Drug_Targets|Pharmaceutical Drug Targets]]&lt;br /&gt;
&lt;br /&gt;
==3D Printed Physical Model of the Influenza Virus==&lt;br /&gt;
&lt;br /&gt;
Shown below is a 3D printed physical model of the Influenza Virus.  The membrane is yellow, the neuraminidase proteins are pink, the hemagglutinin proteins are purple, and the proton pump proteins are light blue. The model has been designed with an opening to allow the schematic addition or removing of genome segments.&lt;br /&gt;
 &lt;br /&gt;
&lt;br /&gt;
[[Image:haVirus_1_centerForBiomolecularModeling.jpg | 750px]]&lt;br /&gt;
&lt;br /&gt;
====The MSOE Center for BioMolecular Modeling====&lt;br /&gt;
&lt;br /&gt;
[[Image:CbmUniversityLogo.jpg | left | 100px]]&lt;br /&gt;
&lt;br /&gt;
The [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling] uses 3D printing technology to create physical models of protein and molecular structures, making the invisible molecular world more tangible and comprehensible. To view more protein structure models, visit our [http://cbm.msoe.edu/educationalmedia/modelgallery/ Model Gallery].&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Immunodeficiency_virus_protease&amp;diff=4395852</id>
		<title>Immunodeficiency virus protease</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Immunodeficiency_virus_protease&amp;diff=4395852"/>
		<updated>2025-11-28T14:26:46Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;StructureSection load=&#039;2nmz&#039; size=&#039;350&#039; side=&#039;right&#039; background=&#039;none&#039; scene=&#039;User:David_Canner/Sandbox_HIV/Opening/2&#039; caption=&#039;Structure of HIV-1 Protease (PDB code [[2nmz]])&#039;&amp;gt;&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Function== &lt;br /&gt;
[[Human Immunodeficiency Virus]] (HIV) is the cause of Acquired Immunodeficiency Syndrome (AIDS). HIV directs the synthesis of several polyproteins, which each consist of several tandemly linked proteins. The maturation of the virus to its infectious form requires that  these polyproteins be cleaved to their component proteins. &amp;lt;scene name=&#039;User:David_Canner/Sandbox_HIV/Opening/2&#039;&amp;gt;HIV-1 protease&amp;lt;/scene&amp;gt;, a homodimeric enzyme, is responsible for doing so and is therefore crucial to the virus&#039;s infectious capacity.&amp;lt;br /&amp;gt;&lt;br /&gt;
HIV exists in two types &#039;&#039;&#039;HIV-1&#039;&#039;&#039; and &#039;&#039;&#039;HIV-2&#039;&#039;&#039;.  HIV-2 infects ca. 30% of AIDS patients vs. 70% infected by HIV-1&amp;lt;ref&amp;gt;PMID:22238126&amp;lt;/ref&amp;gt;.&amp;lt;br /&amp;gt;&lt;br /&gt;
&#039;&#039;&#039;FIV&#039;&#039;&#039; is Feline Immunodeficiency virus protease.&amp;lt;br /&amp;gt;&lt;br /&gt;
&#039;&#039;&#039;SIV&#039;&#039;&#039; is Simian Immunodeficiency virus protease.&amp;lt;br /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
See also:[[Flaps Morph for HIV Protease]].&lt;br /&gt;
&lt;br /&gt;
==Structure of HIV-1 Protease==&lt;br /&gt;
The X-ray structure of HIV-1 protease&amp;lt;ref&amp;gt;PMID:2548279&amp;lt;/ref&amp;gt;&amp;lt;ref&amp;gt;PMID:2682266&amp;lt;/ref&amp;gt; reveals that it is composed of &amp;lt;scene name=&#039;User:David_Canner/Sandbox_HIV/Identical_subunits/1&#039;&amp;gt;two symmetrically related subunits&amp;lt;/scene&amp;gt;, each consisting of 99 amino acid residues. The subunits come together in such as way as to &amp;lt;scene name=&#039;User:David_Canner/Sandbox_HIV/Tunnel/1&#039;&amp;gt;form a tunnel where they meet&amp;lt;/scene&amp;gt;. This tunnel is of critical importance because the active site of the protease is located  in its interior. The active site consists of &amp;lt;scene name=&#039;User:David_Canner/Sandbox_HIV/Catalytic_triad/3&#039;&amp;gt; two Asp-Thr-Gly conserved sequences&amp;lt;/scene&amp;gt;, making it a member of the aspartyl protease family. The two Asp&#039;s are &amp;lt;scene name=&#039;User:David_Canner/Sandbox_HIV/Catalytic_asp/1&#039;&amp;gt;essential catalytic residues&amp;lt;/scene&amp;gt; either interact with the incoming water OR protonate the carbonyl to make the carbon more electrophilic for the incoming &amp;lt;scene name=&#039;31/315240/Saquinavir_cat_water/2&#039;&amp;gt;water&amp;lt;/scene&amp;gt;. You may be wondering how a polyprotein makes its way into the active-site tunnel, as the&amp;lt;scene name=&#039;User:David_Canner/Sandbox_HIV/Narrow_tunnel/1&#039;&amp;gt; tunnel appears to be too narrow &amp;lt;/scene&amp;gt; to admit it. The key is the two flexible flaps on the top of the tunnel that &amp;lt;scene name=&#039;User:David_Canner/Sandbox_HIV/Hiv_tunnel_morph/3&#039;&amp;gt;move to allow proteins &amp;lt;/scene&amp;gt;to enter the tunnel. The flaps &amp;lt;scene name=&#039;User:David_Canner/Sandbox_HIV/Hiv_tunnel_morph_flaps/2&#039;&amp;gt;undergo a dramatic movement&amp;lt;/scene&amp;gt;, shifting from an open to a closed conformation to bind the target in an appropriate conformation for cleavage. This is more clearly seen at [[Flaps Morph for HIV Protease]].&lt;br /&gt;
&lt;br /&gt;
==Medical Implications==&lt;br /&gt;
There currently is no cure or vaccine against HIV.  Researchers, however, have discovered treatments that can halt and even reverse the progression of AIDS, due in large part to our understanding of the structure of HIV-1 protease. &amp;lt;scene name=&#039;User:David_Canner/Sandbox_HIV/Saquinavir/4&#039;&amp;gt;Saquinavir&amp;lt;/scene&amp;gt; ([[Invirase]]) was the first protease inhibitor approved by the FDA for the treatment of HIV. It inhibits HIV protease by &amp;lt;scene name=&#039;User:David_Canner/Sandbox_HIV/Saquinavir_tunnel/1&#039;&amp;gt;binding tightly in the active site tunnel&amp;lt;/scene&amp;gt;, preventing the binding  of polyproteins. Its chemical structure mimics the tetrahedral intermediate of the hydrolytic reaction, thereby  &amp;lt;scene name=&#039;User:David_Canner/Sandbox_HIV/Saquinavir_cat/3&#039;&amp;gt;interacting strongly with the catalytic Asp residues&amp;lt;/scene&amp;gt;.&amp;lt;ref&amp;gt;PMID:17243183&amp;lt;/ref&amp;gt; Saquinavir is essentially an uncleavable ligand, as indicated by the &amp;lt;scene name=&#039;User:David_Canner/Sandbox_HIV/Hiv_morph2/9&#039;&amp;gt; similar conformational changes in the protease flaps &amp;lt;/scene&amp;gt; on binding saquinavir or a polypeptide.  Resistance to saquinavir is due to alterations in the HIV protease sequence, including the mutation of &amp;lt;scene name=&#039;31/315240/Saquinavir_mut/1&#039;&amp;gt;Leu 10 and Ile 50&amp;lt;/scene&amp;gt;&amp;lt;ref&amp;gt;PMID: 8969180&amp;lt;/ref&amp;gt;. Drugs used to treat HIV infection that inhibit &amp;lt;scene name=&#039;User:David_Canner/Sandbox_HIV/Inhibitor_intro/1&#039;&amp;gt;HIV protease&amp;lt;/scene&amp;gt; include &amp;lt;scene name=&#039;User:David_Canner/Sandbox_HIV/Indinavir/2&#039;&amp;gt;Indinavir &amp;lt;/scene&amp;gt; ([[Crixivan]]), &amp;lt;scene name=&#039;User:David_Canner/Sandbox_HIV/Ritonavir/1&#039;&amp;gt;Ritonavir&amp;lt;/scene&amp;gt; ([[Norvir]]), [[Saquinavir]], [[Tipranavir]], [[Amprenavir]] (Agenerase), [[Atazanavir]] (Rayataz), [[Darunavir]] (Prezista), [[Fosamprenavir]] (Lexiva or Telzir), [[Lopinavir]] (Kaletra), [[Nelfinavir]] (Viracept) and &amp;lt;scene name=&#039;User:David_Canner/Sandbox_HIV/Nelfinavir/2&#039;&amp;gt;Nelfinavir&amp;lt;/scene&amp;gt; ([[Viracept]]). &lt;br /&gt;
&lt;br /&gt;
See also [[Treatments:HIV Protease Inhibitor Pharmacokinetics References]]&lt;br /&gt;
&lt;br /&gt;
==  Structural Insights into the South African HIV-1 Subtype C Protease: Impact of hinge region dynamics and flap flexibility in drug resistance &amp;lt;ref&amp;gt;doi 10.1080/07391102.2012.736774&amp;lt;/ref&amp;gt;==&lt;br /&gt;
The current study reports on the apo crystal structure of the &amp;lt;scene name=&#039;Journal:JBSD:36/Cv/3&#039;&amp;gt;South African HIV-1 subtype C protease (C-SA PR)&amp;lt;/scene&amp;gt;. Structure of &amp;lt;scene name=&#039;Journal:JBSD:36/Cv/4&#039;&amp;gt;unbound HIV-1 PR&amp;lt;/scene&amp;gt; with the active site triplet (D25, T26 and G27) shown in ball-and-stick representation, &amp;lt;font color=&#039;magenta&#039;&amp;gt;&amp;lt;b&amp;gt;hinge region in magenta (residues 35–42 and 57–61)&amp;lt;/b&amp;gt;&amp;lt;/font&amp;gt;, and &amp;lt;span style=&amp;quot;color:cyan;background-color:black;font-weight:bold;&amp;quot;&amp;gt;flap region (residues 46–54) in cyan&amp;lt;/span&amp;gt;. The relevance of this study cannot be underestimated because South Africa is at the epicenter of the HIV/AIDS pandemic. A detailed understanding of the molecular interactions between the drug and its target is required if we are to improve the design of protease inhibitors (PIs). Our study indicated that the loss of a salt bridge between &amp;lt;scene name=&#039;Journal:JBSD:36/Cv/5&#039;&amp;gt;residues E35 and R57&amp;lt;/scene&amp;gt; at the hinge region affects the flap dynamics of the apo C-SA PR which may reduce the affinity and, therefore, the efficacy of the current protease inhibitors toward the C-SA PR (&amp;lt;span style=&amp;quot;color:deeppink;background-color:black;font-weight:bold;&amp;quot;&amp;gt;subtype C-SA PR is in deeppink&amp;lt;/span&amp;gt;, [[3u71]] and &amp;lt;span style=&amp;quot;color:yellow;background-color:black;font-weight:bold;&amp;quot;&amp;gt;subtype B PR is in yellow&amp;lt;/span&amp;gt;, [[2pc0]]). &amp;lt;scene name=&#039;Journal:JBSD:36/Cv/6&#039;&amp;gt;Structural alignment&amp;lt;/scene&amp;gt; of of the &amp;lt;span style=&amp;quot;color:deeppink;background-color:black;font-weight:bold;&amp;quot;&amp;gt;C-SA PR (deep pink&amp;lt;/span&amp;gt;, PDB ID: [[3u71]]), &amp;lt;span style=&amp;quot;color:yellow;background-color:black;font-weight:bold;&amp;quot;&amp;gt;consensus subtype B PR (yellow&amp;lt;/span&amp;gt;, PDB ID: [[2pc0]]), and &amp;lt;span style=&amp;quot;color:wheat;background-color:black;font-weight:bold;&amp;quot;&amp;gt;subtype B-MDR PR (color wheat&amp;lt;/span&amp;gt;, PDB ID: [[1rp1]]) reveals that the PRs under investigation do not differ significantly. The crystal structure of the C-SA PR will serve as a foundation to improve the rational design of PIs which will have a greater impact on anti-retroviral chemotherapy in sub-Saharan Africa.&lt;br /&gt;
&lt;br /&gt;
==3D Printed Physical Model of HIV Protease==&lt;br /&gt;
&lt;br /&gt;
Shown below are 3D printed physical models of HIV Protease. Both versions are shown in alpha carbon format, with select side chains shown colored by element, with carbon gray, nitrogen blue, oxygen red and sulfur yellow.  Both models have been designed with precisely embedded magnets that allow the two chains to pull apart into individual pieces. &lt;br /&gt;
&lt;br /&gt;
[[Image:hivProtease1_centerForBioMolecularModeling_crop.jpg|230px]]       [[Image:800px-HivProtease2 centerForBioMolecularModeling Crop.jpg|230px]]&lt;br /&gt;
&lt;br /&gt;
The MSOE Center for BioMolecular Modeling&lt;br /&gt;
&lt;br /&gt;
[[Image:CbmUniversityLogo.jpg | left | 150px]]&lt;br /&gt;
&lt;br /&gt;
The [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling] uses 3D printing technology to create physical models of protein and molecular structures, making the invisible molecular world more tangible and comprehensible. To view more protein structure models, visit our [http://cbm.msoe.edu/educationalmedia/modelgallery/ Model Gallery].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==HIV Protease Movie==&lt;br /&gt;
&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;br&amp;gt; HIV Protease Movie by Warren L. DeLano (made via PyMol)&lt;br /&gt;
&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;html5media height=“500” width=“1000”&amp;gt;https://www.youtube.com/embed/iSeVYYDvLCk&amp;lt;/html5media&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Additional resources==&lt;br /&gt;
*&#039;&#039;Aids Before Protease Inhibitors&#039;&#039; and &#039;&#039;HIV Protease Inhibitors: A Breakthrough&#039;&#039; at [[Molecular Playground/HIV Protease Inhibitor|HIV Protease Inhibitor]].&lt;br /&gt;
*[[Flaps Morph for HIV Protease]]&lt;br /&gt;
*[[HIV Protease Inhibitor Pharmacokinetics]]&lt;br /&gt;
*[[Treatments:HIV Protease Inhibitor Pharmacokinetics References]]&lt;br /&gt;
*[[HIV Protease Inhibitor Resistance Profile]]&lt;br /&gt;
*[[HIV Protease Resistance]]&lt;br /&gt;
*[[Viability of a drug-resistant HIV-1 protease mutant]]&lt;br /&gt;
*[[HIV and accessory proteins]]&lt;br /&gt;
*[[Treatments:HIV Protease Inhibitor Pharmacokinetics References]]&lt;br /&gt;
*[[Group:SMART:HIV-1 Subtype C Protease]]&lt;br /&gt;
*[[Human Immunodeficiency Virus]]&lt;br /&gt;
*[[Ann Taylor/HIV Protease]]&lt;br /&gt;
*[[Virus protease]]&lt;br /&gt;
*[[HIV-1 protease]]&lt;br /&gt;
*[[Protease]]&lt;br /&gt;
*[[Viability of a drug-resistant HIV-1 protease mutant]]&lt;br /&gt;
* Structural Insights into the South African HIV-1 Subtype C Protease: Impact of hinge region dynamics and flap flexibility in drug resistance &amp;lt;ref&amp;gt;doi 10.1080/07391102.2012.736774&amp;lt;/ref&amp;gt;&lt;br /&gt;
* [http://cdn.rcsb.org/pdb101/learn/resources/structural-biology-of-hiv/index.html Structural Biology of HIV], an interactive Flash graphic of the virion with explanations of its components.&lt;br /&gt;
&lt;br /&gt;
==Immunodeficiency virus protease 3D structures==&lt;br /&gt;
[[Immunodeficiency virus protease 3D structures]]&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
[[Category:Topic Page]]&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Green_Fluorescent_Protein&amp;diff=4395851</id>
		<title>Green Fluorescent Protein</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Green_Fluorescent_Protein&amp;diff=4395851"/>
		<updated>2025-11-28T14:26:11Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;StructureSection load=&#039;1ema&#039; size=&#039;350&#039; side=&#039;right&#039; scene=&#039;Green_Fluorescent_Protein/1ema_gfp_default/2&#039; caption=&#039;Green fluorescent protein complex with peptide-derived chromophore ([[1ema]])&#039; &amp;gt;&lt;br /&gt;
==Function==&lt;br /&gt;
&#039;&#039;&#039;Green fluorescent protein (GFP)&#039;&#039;&#039; is a bioluminescent polypeptide consisting of 238 residues isolated from the body of &#039;&#039;Aequorea victoria&#039;&#039; jellyfish.&amp;lt;ref name=&amp;quot;PDBsum&amp;quot;&amp;gt;[http://www.ebi.ac.uk/thornton-srv/databases/cgi-bin/pdbsum/GetPage.pl?pdbcode=1ema&amp;amp;template=main.html], Protein Database (PDBsum): 1ema.  European Bioinformatics (EBI); 2009.&amp;lt;/ref&amp;gt; GFP converts the blue chemiluminescent of aequorin in the jellyfish into green fluorescent light.&amp;lt;ref name=&amp;quot;Yang&amp;quot;&amp;gt;[http://www-bioc.rice.edu/Bioch/Phillips/Papers/gfpbio.html], Yang F, Moss LG, Phillips GN Jr.  1996.  The molecular structure of green fluorescent protein.  Biotechnology.  14: 1246-1251.  DOI 10.1038/nbt1096-1246.&amp;lt;/ref&amp;gt; It remains unclear why these jellyfish use fluorescence, why green is better than blue, or why they produce a separate protein for green fluorescence as opposed to simply mutating the present aequorin to shift its wavelength,&amp;lt;ref name=&amp;quot;Tsien&amp;quot; /&amp;gt; but in the laboratory, GFP can be incorporated into a variety of biological systems in order to function as a marker protein. Since its discovery in 1962, GFP has come to play a significant role in research as a tool to monitor gene expression, cellular localization, protein mobility, intracellular trafficking, and interactions between various membrane and cytoplasmic proteins, as well as many others. &lt;br /&gt;
* &#039;&#039;&#039;Superfolder GFP&#039;&#039;&#039; does not misfold when fused to other proteins.&lt;br /&gt;
*&#039;&#039;&#039;Photoconvertible fluorescent protein&#039;&#039;&#039; changes the emission when exposed to UV light&amp;lt;ref&amp;gt;PMID:32242924&amp;lt;/ref&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
See also&amp;lt;br /&amp;gt;&lt;br /&gt;
[[Green Fluorescent Protein: Research Tool]].&amp;lt;ref name=&amp;quot;Haldar&amp;quot;&amp;gt; [http://www.springerlink.com/content/wvg513864266g77n/fulltext.pdf], Haldar S, Chattopadhyay A.  2009.  The green journey.  J Fluoresc.  19:1-2.  DOI 10.1007/s10895-008-0455-6; biographical background on [http://en.wikipedia.org/wiki/Douglas_Prasher Douglas Prasher], [http://en.wikipedia.org/wiki/Martin_Chalfie Martin Chalfie] and [http://en.wikipedia.org/wiki/Roger_Tsien Roger Tsien].&amp;lt;/ref&amp;gt;&amp;lt;br /&amp;gt;&lt;br /&gt;
[[Colored &amp;amp; Bioluminescent Protein]]&amp;lt;br /&amp;gt;&lt;br /&gt;
For&#039;&#039;&#039; red fluorescent protein&#039;&#039;&#039; see [[MCherry Fluorescent Protein]].&amp;lt;br /&amp;gt;&lt;br /&gt;
In Hebrew: [[GFP (Hebrew)]] and [[Gfp vc2]].&lt;br /&gt;
&lt;br /&gt;
==History==&lt;br /&gt;
&#039;&#039;Aequorea victoria&#039;&#039; was first discovered and investigated for its bioluminescence by Frank Johnson, who invited Osamu Shimomura to work with him in on a small island not far from British Columbia, where the jellyfish is abundant.&amp;lt;ref name=&amp;quot;Shimomura&amp;quot;&amp;gt;[http://nobelprize.org/nobel_prizes/chemistry/laureates/2008/shimomura_lecture.pdf], Shimomura O.  The discovery of green fluorescent protein.  Nobel Prize Lecture; 2009;; biographical background at [http://en.wikipedia.org/wiki/Osamu_Shimomura Wikipedia].&amp;lt;/ref&amp;gt; Found off the west coast of the United States between British Columbia and central California,&amp;lt;ref name=&amp;quot;Cowles&amp;quot;&amp;gt;[http://www.wallawalla.edu/academics/departments/biology/rosario/inverts/Cnidaria/Class-Hydrozoa/Hydromedusae/Aequorea_victoria.html],Cowles D, Cowles J.  &#039;&#039;Aequorea victoria&#039;&#039;.  2007.  Walla Wall University.&amp;lt;/ref&amp;gt; the jellyfish was considered a local phenomenon as it would drift in and out of the harbors.&amp;lt;ref name=&amp;quot;Shimomura&amp;quot; /&amp;gt;&lt;br /&gt;
[[Image:GFP mice.png|thumb|left|450x200px|Mice with GFP inserted into their genomes for neurology studies.]]&lt;br /&gt;
&lt;br /&gt;
Shimomura was originally looking only to isolate the blue luminescent protein of &#039;&#039;Aequorea victoria&#039;&#039;, traditionally thought to be [[luciferase]], but it would soon become apparent that the glow was in fact due to aequorin, a substance related, but slightly varying from luciferase.&amp;lt;ref name=&amp;quot;Haldar&amp;quot; /&amp;gt;&amp;lt;ref name=&amp;quot;Shimomura&amp;quot; /&amp;gt; However, the light emitted from aequorin still differed from the light emitted from the wild jellyfish. This quandary led to the discovery of the green fluorescent protein responsible for this disparity, but sufficient amounts of the protein could not be collected for study until 1979. The journey to discover the nature of GFP had begun.&amp;lt;ref name=&amp;quot;Shimomura&amp;quot; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
In the 1990’s, Douglas Prasher, Frank Prendergast, and co-workers successfully cloned the gene that encoded for GFP.  Martin Chalfie further pursued this line of work and was eventually able to express GFP in heterologous systems such as E. coli and C. elegans.  Chalfie’s research provided the first evidence that GFP was unique as it did not require the presence of any exogenous substance or cofactor for fluorescence.&amp;lt;ref name=&amp;quot;Haldar&amp;quot; /&amp;gt; The lack for the need for a cofactor proved that the cloned GFP gene contained all the information necessary for posttranslational synthesis of the chromophore. &amp;lt;ref name=&amp;quot;Tsien&amp;quot; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Roger Tsien and co-workers were intrigued by the absence of a necessary cofactor and began to research the structure of GFP and how it relates to its fluorescence.  They discovered that a helix within the beta barrel structure of GFP actually contained a fluorophore responsible for fluorescence.  In researching its structure, they were able to develop GFP derivatives with improved fluorescence and photo-stability.  Shimomura, Chalfie, and Tsien were each recognized for their work involving GFP with the Nobel Prize in 2008.&amp;lt;ref name=&amp;quot;Haldar&amp;quot; /&amp;gt;  In the time since the work of these three researchers, GFP has been successfully expressed and utilized in bacteria, yeast, slime mold, plants, drosophila fruit flies, zebra-fish, and mammalian cells.&amp;lt;ref name=&amp;quot;Yang&amp;quot; /&amp;gt;  Below, mice have had GFP inserted into their genomes for studies in neurology.&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
===Primary &amp;amp; Secondary Structure===&lt;br /&gt;
&lt;br /&gt;
Green fluorescent protein (&amp;lt;scene name=&#039;Green_Fluorescent_Protein/1ema_gfp_default/2&#039;&amp;gt;default scene&amp;lt;/scene&amp;gt;) is a 21 kDa protein consisting of 238 residues strung together&amp;lt;ref&amp;gt;Primary structure at [http://www.ebi.ac.uk/thornton-srv/databases/cgi-bin/pdbsum/GetPage.pl?pdbcode=1ema&amp;amp;template=protein.html&amp;amp;r=wiring&amp;amp;l=1&amp;amp;chain=A www.ebi.aci.uk].&amp;lt;/ref&amp;gt; to form a  &lt;br /&gt;
&amp;lt;scene name=&#039;Green_Fluorescent_Protein/1ema_gfp_barrel/2&#039;&amp;gt;secondary structure&amp;lt;/scene&amp;gt; of five α-helices and one eleven-stranded β-pleated sheet,&amp;lt;ref name=&amp;quot;PDBsum&amp;quot; /&amp;gt; where each strand contains nine to thirteen residues each.&amp;lt;ref name=&amp;quot;Ormo&amp;quot; /&amp;gt;  (To view the primary and secondary structure of GFP, go to https://www.rcsb.org/pdb/explore/remediatedSequence.do?structureId=1EMA.)  These β-strands display an almost “seamless symmetry” in which only two of the strands vary in structural content.&amp;lt;ref name=&amp;quot;Phillips&amp;quot;&amp;gt;PMID: 9434902&amp;lt;/ref&amp;gt;  This β-sheet conforms itself through regular hydrogen bonding into a β-barrel.&amp;lt;ref name=&amp;quot;Yang&amp;quot; /&amp;gt;  In GFP, the structure is so regular that &amp;lt;scene name=&#039;Green_Fluorescent_Protein/Water_stripes/1&#039;&amp;gt;&amp;quot;stripes&amp;quot;&amp;lt;/scene&amp;gt; of water molecules (red) can be seen following the structure of the barrel.&amp;lt;ref name=&amp;quot;Phillips&amp;quot; /&amp;gt;  Together with the α-helices at either end of the molecule, a nearly perfect cylinder is produced, 42Å long and 24Å in diameter,&amp;lt;ref name=&amp;quot;Ormo&amp;quot; /&amp;gt; creating what is referred to as a “β-can” formation.&amp;lt;ref name=&amp;quot;Phillips&amp;quot; /&amp;gt;  The short helical segments at either end of the cylinder form “caps” to further protect the interior of the β-barrel.&amp;lt;ref name=&amp;quot;Phillips&amp;quot; /&amp;gt;  Overall stability is maintained by this β-can structure, helping to resist unfolding from heat and other denaturants.&amp;lt;ref name=&amp;quot;Yang&amp;quot; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
One &amp;lt;jmol&amp;gt;&amp;lt;jmolLink&amp;gt;&amp;lt;script&amp;gt;script &amp;quot;/scripts/Green_Fluorescent_Protein/Central_helix/1.spt&amp;quot;; ppdiaCaptionCmd = &amp;quot;changeCaption(&#039;The central helix (shown in red) contains the fluorophore and runs through the barrel (shown as white transparent strands) along its axis (PDB-ID [[1ema]]). &#039;,&#039;white&#039;,&#039;black&#039;);&amp;quot;;javascript @ppdiaCaptionCmd;model 2;&amp;lt;/script&amp;gt;&amp;lt;text&amp;gt;α-helix&amp;lt;/text&amp;gt;&amp;lt;/jmolLink&amp;gt;&amp;lt;/jmol&amp;gt; can be found running through the central axis of the β-barrel,&amp;lt;ref name=&amp;quot;Haldar&amp;quot; /&amp;gt; roughly &amp;lt;scene name=&#039;Green_Fluorescent_Protein/Perpendicular/1&#039;&amp;gt;perpendicular&amp;lt;/scene&amp;gt; to the symmetry axis of the barrel.&amp;lt;ref name=&amp;quot;Ormo&amp;quot;&amp;gt;Ormo M, Cubitt AB, Kallio K, Gross LA, Tsien RY, Remington SJ.  1996.  Crystal structure of the &#039;&#039;Aequorea victoria&#039;&#039; green fluorescent protein.  Science.  273(5280):1392-1395.  DOI 10.1126/science.273.5280.1392.&amp;lt;/ref&amp;gt;  This helix is extremely important as it contains the fluorophore responsible for fluorescence.&amp;lt;ref name=&amp;quot;Yang&amp;quot; /&amp;gt;&amp;lt;ref name=&amp;quot;Haldar&amp;quot; /&amp;gt;  &lt;br /&gt;
&lt;br /&gt;
The fluorophore is part of the polypeptide chain (i.e. covalently connencted). If you press the buttom below, it will show the connection.&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
&amp;lt;jmolButton&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;select (64.C or 66.N1 or 66.C3 or 68.N); connect 1.1 1.6; select 64, 66, 68; wireframe 0.2; &amp;lt;/script&amp;gt;&lt;br /&gt;
  &amp;lt;text&amp;gt;make bonds&amp;lt;/text&amp;gt;&lt;br /&gt;
&amp;lt;/jmolButton&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
This α-helix in particular is highly stabilized by the many &amp;lt;scene name=&#039;10/100139/Spacefill/1&#039;&amp;gt;hydrophobic contacts&amp;lt;/scene&amp;gt; that are made with each strand of the barrel.&amp;lt;ref name=&amp;quot;Andrews&amp;quot;&amp;gt;PMID:18713871&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===The Chromophore===&lt;br /&gt;
&lt;br /&gt;
The &amp;lt;scene name=&#039;10/100139/Chromophore/2&#039;&amp;gt;chromophore&amp;lt;/scene&amp;gt; (&amp;lt;scene name=&#039;10/100139/Green_fluorescent_protein/1&#039;&amp;gt;top view&amp;lt;/scene&amp;gt;) of GFP is located at the center of the β-barrel with a wild-type excitation peak of 395 nm, and a minor peak at 475 nm (about three times less intense&amp;lt;ref name=&amp;quot;Tsien&amp;quot; /&amp;gt;) &amp;lt;ref name=&amp;quot;Yang&amp;quot; /&amp;gt;&amp;lt;ref name=&amp;quot;Cubitt&amp;quot; /&amp;gt;&amp;lt;ref name=&amp;quot;Ormo&amp;quot; /&amp;gt;&amp;lt;ref name=&amp;quot;Phillips&amp;quot; /&amp;gt; with extinction coefficients of approximately 30,000 and 7,000 M&amp;lt;sup&amp;gt;-1&amp;lt;/sup&amp;gt; cm&amp;lt;sup&amp;gt;-1&amp;lt;/sup&amp;gt;, respectively.&amp;lt;ref name=&amp;quot;Yang&amp;quot; /&amp;gt;&amp;lt;ref name=&amp;quot;Phillips&amp;quot; /&amp;gt;  Interestingly, the &#039;&#039;Aequorea victoria&#039;&#039; jellyfish utilizes the smaller of the two excitation peaks as pure aequorin emits a light of 470 nm.&amp;lt;ref name=&amp;quot;Tsien&amp;quot;&amp;gt;Tsien, Roger Y.  1998.  The Green Fluorescent Protein.  Annual Review in Biochemistry.  67:509-544.&amp;lt;/ref&amp;gt;  The relative amplitudes of these two excitation peaks can vary depending on environmental factors and previous illumination.&amp;lt;ref name=&amp;quot;Ormo&amp;quot; /&amp;gt;  For example, continued excitation leads to a diminution of the 395 nm excitation peak with a reciprocal amplification of the 475 nm peak.&amp;lt;ref name=&amp;quot;Phillips&amp;quot; /&amp;gt;  Regardless of absorption, the chromophore of GFP emits light of 508 nm.&amp;lt;ref name=&amp;quot;Yang&amp;quot; /&amp;gt;&amp;lt;ref name=&amp;quot;Cubitt&amp;quot; /&amp;gt;&amp;lt;ref name=&amp;quot;Ormo&amp;quot; /&amp;gt;&amp;lt;ref name=&amp;quot;Phillips&amp;quot; /&amp;gt;  &lt;br /&gt;
&lt;br /&gt;
Three amino residues in the central α-helix constitute the fluorophore of GFP: Ser&amp;lt;sup&amp;gt;65&amp;lt;/sup&amp;gt;Tyr&amp;lt;sup&amp;gt;66&amp;lt;/sup&amp;gt;Gly&amp;lt;sup&amp;gt;67&amp;lt;/sup&amp;gt; (see below) or of EGFP: of GFP: Thr&amp;lt;sup&amp;gt;65&amp;lt;/sup&amp;gt;Tyr&amp;lt;sup&amp;gt;66&amp;lt;/sup&amp;gt;Gly&amp;lt;sup&amp;gt;67&amp;lt;/sup&amp;gt;.  Tsien et al. discovered that this tri-peptide sequence is post-translationally modified by internal cyclization and oxidation&amp;lt;ref name=&amp;quot;Haldar&amp;quot; /&amp;gt; to produce a &amp;lt;scene name=&#039;10/100139/Chromophore_structure/3&#039;&amp;gt;4-(p-hydroxybenzylidene)-imidazolidin-5-one&amp;lt;/scene&amp;gt; structure (highlight atoms from &amp;lt;jmol&amp;gt;&amp;lt;jmolLink&amp;gt;&amp;lt;script&amp;gt; select (*.C1, *.CA1, *.N1, *.CB1, *.CG1, *.OG1) and 66; selectionHalos ON; delay 1.5;selectionHalos OFF;&amp;lt;/script&amp;gt;&amp;lt;text&amp;gt;⚞Thr 65⚟&amp;lt;/text&amp;gt;&amp;lt;/jmolLink&amp;gt; &amp;lt;/jmol&amp;gt;, &amp;lt;jmol&amp;gt;&amp;lt;jmolLink&amp;gt;&amp;lt;script&amp;gt; select (*.C2, *.O2, *.CA2, *.N2, *.CB2, *.CG2, *.CD1, *.CD2, *.CE1, *.CE2, *.CZ, *.OH) and 66; selectionHalos ON; delay 1.5;selectionHalos OFF;&amp;lt;/script&amp;gt;&amp;lt;text&amp;gt;⚞Tyr 66⚟&amp;lt;/text&amp;gt;&amp;lt;/jmolLink&amp;gt; &amp;lt;/jmol&amp;gt;, &amp;lt;jmol&amp;gt;&amp;lt;jmolLink&amp;gt;&amp;lt;script&amp;gt; select (*.O3,*.C3,*.CA3,*.N3) and 66; selectionHalos ON; delay 1.5;selectionHalos OFF;&amp;lt;/script&amp;gt;&amp;lt;text&amp;gt;⚞Gly 67⚟&amp;lt;/text&amp;gt;&amp;lt;/jmolLink&amp;gt;&amp;lt;/jmol&amp;gt;).&amp;lt;ref name=&amp;quot;Yang&amp;quot; /&amp;gt;  Studies with E. coli proposed a sequential mechanism for the formation of the fluorophore that was initiated by a rapid cyclization between Ser&amp;lt;sup&amp;gt;65&amp;lt;/sup&amp;gt; and Gly&amp;lt;sup&amp;gt;67&amp;lt;/sup&amp;gt; to form an imidazolin-5-one intermediate.&amp;lt;ref name=&amp;quot;Yang&amp;quot; /&amp;gt;  This rapid cyclization is carried out via nucleophilic attack of the amino group from Gly&amp;lt;sup&amp;gt;67&amp;lt;/sup&amp;gt; on the carbonyl group of Ser&amp;lt;sup&amp;gt;65&amp;lt;/sup&amp;gt; to form a five-membered ring.  The loss of water then forms the imidazolin-5-one intermediate.&amp;lt;ref name=&amp;quot;Cubitt&amp;quot; /&amp;gt;  Cyclization is succeeded by a much slower rate-limiting oxygenation of the Tyr&amp;lt;sup&amp;gt;66&amp;lt;/sup&amp;gt; hydroxybenzyl side chain by atmospheric oxygen (No fluorescence was seen in anaerobically grown E. coli.), resulting in the 4-(p-hydroxybenzylidene)-imidazolidin-5-one stucture.&amp;lt;ref name=&amp;quot;Yang&amp;quot; /&amp;gt;&amp;lt;ref name=&amp;quot;Cubitt&amp;quot; /&amp;gt;&amp;lt;ref name=&amp;quot;Phillips&amp;quot; /&amp;gt;  The double bond that results from this series of reactions results in the linkage of the two π-systems of the rings, forming a &amp;lt;scene name=&#039;10/100139/Chromophore/5&#039;&amp;gt;larger conjugated system&amp;lt;/scene&amp;gt; essential for fluorophore stability. &amp;lt;ref name=&amp;quot;Bublitz&amp;quot;&amp;gt; Bublitz G, King BA, Boxer SG.  1998.  Electronic structure of the chromophore in green fluorescent protein (GFP).  Journal of the American Chemical Society.  120(36): 9370-9371.  DOI 10.1021/ja98160e.&amp;lt;/ref&amp;gt;&lt;br /&gt;
[[Image:GFP Chromophore.png|center|489x360px]]&lt;br /&gt;
&lt;br /&gt;
The process is completely auto-catalytic such that there are no known co-factors or enzymatic components required.&amp;lt;ref name=&amp;quot;Yang&amp;quot; /&amp;gt;  Despite the stability of the final product, while the chromophore is forming, the environmental temperature cannot drop below 30°C or the yield of viable GFP will decrease substantially.&amp;lt;ref name=&amp;quot;Yang&amp;quot; /&amp;gt;&amp;lt;ref name=&amp;quot;Phillips&amp;quot; /&amp;gt;  This, of course, is not an issue for the protein in nature as the jellyfish is unlikely to encounter waters of this degree in the Pacific Northwest.&amp;lt;ref name=&amp;quot;Tsien&amp;quot; /&amp;gt;  Such a temperature sensitivity is only relevant during formation as the stability of the final product is maintained through a network of close contacts surrounding the fluorophore.&amp;lt;ref name=&amp;quot;Yang&amp;quot; /&amp;gt;  This, however, can and has been used in [[pulse-chase experiments]] in which the GFP-expressing cells are exposed to varying temperatures in place of labeled vs. unlabeled trials.&amp;lt;ref name=&amp;quot;Tsien&amp;quot; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
As the central α-helix is not located directly in the center of the β-barrel, cavities of differing area exist on either side of the chromophore.  The larger cavity, consisting of about 135 cubic Å,&amp;lt;ref name=&amp;quot;Ormo&amp;quot; /&amp;gt; does not open out to the bulk solvent, but rather houses &amp;lt;scene name=&#039;Green_Fluorescent_Protein/Water_molecules/1&#039;&amp;gt;four water molecules&amp;lt;/scene&amp;gt;.&amp;lt;ref name=&amp;quot;Ormo&amp;quot; /&amp;gt;&amp;lt;ref name=&amp;quot;Van&amp;quot;&amp;gt;van Thor JJ, Sage, JT.  2006.  Charge transfer in green fluorescent protein.  Photochemical &amp;amp; Photobiological Sciences.  5:597-602.  DOI 10.1039/b516525c.&amp;lt;/ref&amp;gt;  Had this space not been occupied, it would be expected to considerably destabilize the protein as a whole.  The hydrogen bonding created by the presence of the water molecules, however, helps to link the buried &amp;lt;scene name=&#039;Green_Fluorescent_Protein/Gln69_glu222/1&#039;&amp;gt;side chains&amp;lt;/scene&amp;gt; of Glu&amp;lt;sup&amp;gt;222&amp;lt;/sup&amp;gt; and Gln&amp;lt;sup&amp;gt;69&amp;lt;/sup&amp;gt; that would otherwise be actively polar.&amp;lt;ref name=&amp;quot;Ormo&amp;quot; /&amp;gt;  Therefore, the water molecules are extremely important in establishing a hydrogen bonding network about the chromophor.&amp;lt;ref name=&amp;quot;Lammich&amp;quot;&amp;gt;PMID: 17040991&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
The opposite side of the chromophore, however, is within close proximity of several aromatic and polar side chains.  Several &amp;lt;scene name=&#039;Green_Fluorescent_Protein/Polar_interactions/2&#039;&amp;gt;polar interactions&amp;lt;/scene&amp;gt; between the surrounding residues and the chromophore are present including: hydrogen bonds of His&amp;lt;sup&amp;gt;148&amp;lt;/sup&amp;gt;, Thr&amp;lt;sup&amp;gt;203&amp;lt;/sup&amp;gt;, and Ser&amp;lt;sup&amp;gt;205&amp;lt;/sup&amp;gt; with the phenolic hydroxyl of Tyr&amp;lt;sup&amp;gt;66&amp;lt;/sup&amp;gt;; Arg&amp;lt;sup&amp;gt;96&amp;lt;/sup&amp;gt; and Gln&amp;lt;sup&amp;gt;94&amp;lt;/sup&amp;gt; with the carbonyl of the imidazolidinone ring; and hydrogen bonds of Glu&amp;lt;sup&amp;gt;222&amp;lt;/sup&amp;gt; with the side chain of Thr&amp;lt;sup&amp;gt;65&amp;lt;/sup&amp;gt;.  Additional hydrogen bonding in the area around the chromophore helps to stabilize Arg&amp;lt;sup&amp;gt;96&amp;lt;/sup&amp;gt; in the protonated form, which suggests the presence of a partial negative charge on the carbonyl oxygen of the imidazolidinone ring in the deprotonated fluorophore.&amp;lt;ref name=&amp;quot;Ormo&amp;quot; /&amp;gt;  Arg&amp;lt;sup&amp;gt;96&amp;lt;/sup&amp;gt; and Gln&amp;lt;sup&amp;gt;94&amp;lt;/sup&amp;gt; in turn help to steady the imidazolidone.&amp;lt;ref name=&amp;quot;Yang&amp;quot; /&amp;gt;  Therefore, it is thought that Arg&amp;lt;sup&amp;gt;96&amp;lt;/sup&amp;gt; is essential for the formation of the fluorophore by catalyzing the initial ring closure.&amp;lt;ref name=&amp;quot;Ormo&amp;quot; /&amp;gt;  Tyr&amp;lt;sup&amp;gt;145&amp;lt;/sup&amp;gt; provides a stabilizing &amp;lt;scene name=&#039;Green_Fluorescent_Protein/Edge_face_interaction/1&#039;&amp;gt;edge-face interaction&amp;lt;/scene&amp;gt;&amp;lt;ref&amp;gt; [http://www.tim.hi-ho.ne.jp/dionisio/ Information about edge-face (CH/π) interactions].&amp;lt;/ref&amp;gt; with the benzyl ring of the chromophore.&amp;lt;ref name=&amp;quot;Ormo&amp;quot; /&amp;gt;  The stability provided by the internal polar interactions are further augmented by the surrounding β-barrel.  &lt;br /&gt;
&lt;br /&gt;
The β-barrel provides a highly constrained environment that protects the chromophore from the bulk solvent,&amp;lt;ref name=&amp;quot;Haldar&amp;quot; /&amp;gt; nearly creating the atmosphere of a vacuum.&amp;lt;ref name=&amp;quot;Lammich&amp;quot; /&amp;gt;  This is most likely responsible for the small [[Stoke’s shift]], or the small wavelength difference between excitation and emission.&amp;lt;ref name=&amp;quot;Ormo&amp;quot; /&amp;gt;  &lt;br /&gt;
&lt;br /&gt;
{{Link Toggle FancyCartoonHighQualityView}}.&lt;br /&gt;
&lt;br /&gt;
Findings show that fluorescence will not occur from a naked chromophore, but rather requires the protection of the β-can structure.&amp;lt;ref name=&amp;quot;Cubitt&amp;quot; /&amp;gt;  However, &#039;&#039;in crystallum&#039;&#039; GFP will exhibit a nearly identical fluorescence spectrum and lifetime when compared with aqueous GFP.  These two elements point to a fluorescence that is not inherent to the isolated fluorophore,&amp;lt;ref name=&amp;quot;Yang&amp;quot; /&amp;gt;&amp;lt;ref name=&amp;quot;Phillips&amp;quot; /&amp;gt; but rather from the auto-catalytic cyclization of the polypeptide sequence Ser&amp;lt;sup&amp;gt;65&amp;lt;/sup&amp;gt;Tyr&amp;lt;sup&amp;gt;66&amp;lt;/sup&amp;gt;Gly&amp;lt;sup&amp;gt;67&amp;lt;/sup&amp;gt; and subsequent oxidation of Tyr&amp;lt;sup&amp;gt;66&amp;lt;/sup&amp;gt;.&amp;lt;ref name=&amp;quot;Phillips&amp;quot; /&amp;gt;  However, this sequence is found in many proteins - why does GFP fluoresce?  According to Phillips (1997), fluorophore formation is due to the close proximity of the backbone atoms between Ser&amp;lt;sup&amp;gt;65&amp;lt;/sup&amp;gt;. and Gly&amp;lt;sup&amp;gt;67&amp;lt;/sup&amp;gt; gained through a lack of sterical hindrance by the hydrogen atom side chain of glycine.  In fact, no functional fluorescent proteins have been found in which any other amino acid other than glycine was found at position 67.  Even so, there are still proteins that have this specific sequence, therefore, there must be another inherent property to GFP that is still left misunderstood.&amp;lt;ref name=&amp;quot;Phillips&amp;quot; /&amp;gt;  &lt;br /&gt;
&lt;br /&gt;
This quandary led Phillips to study the acid/base chemistry catalyzing the initial cyclization of the chromophore.  He found that Arg&amp;lt;sup&amp;gt;96&amp;lt;/sup&amp;gt; actually acts as a &amp;lt;scene name=&#039;Green_Fluorescent_Protein/Arg96/1&#039; &amp;gt;base&amp;lt;/scene&amp;gt; by withdrawing electrons through hydrogen bonding with the carbonyl oxygen of Ser&amp;lt;sup&amp;gt;65&amp;lt;/sup&amp;gt; to activate the carbonyl carbon for nucleophilic attack by the amide nitrogen of Gly&amp;lt;sup&amp;gt;67&amp;lt;/sup&amp;gt;.  This mechanism was further supported by &#039;&#039;ab initio&#039;&#039; calculations, as well as database searches of similar compounds and protein sequences.  Through acid/base chemistry, the chromophore is stabilized by resonance.&amp;lt;ref name=&amp;quot;Phillips&amp;quot; /&amp;gt;  Femtosecond Raman spectroscopy has been used to map the alteration of the structure close the chromophore during excited-state protein transfer and shown that chromophore wagging is orchestrated by the protein environment.&amp;lt;ref name=&amp;quot;Fang&amp;quot;&amp;gt;PMID: 19907490&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Mutant Studies===&lt;br /&gt;
&lt;br /&gt;
Many mutant green fluorescent proteins have been developed in order to further understand the structure and mechanism of the fluorophore.  The first mutagenesis studies simply &lt;br /&gt;
&amp;lt;scene name=&#039;Green_Fluorescent_Protein/Truncated_ends/3&#039; &amp;gt;truncated the ends&amp;lt;/scene&amp;gt; of the amino acid sequence (&amp;lt;scene name=&#039;Green_Fluorescent_Protein/1ema_gfp_barrel/2&#039; &amp;gt;see without truncated ends&amp;lt;/scene&amp;gt;.  NOTE: The structure represented here is already truncated at the carbonyl terminus).  Shortening the polypeptide by more than seven amino acids from either terminus lead to a total loss of fluorescence, as well as a complete failure to absorb light at the traditional wavelengths.   This is most likely due to the structure of the protein.  The last seven amino acid residues of the carboxyl terminus are roughly disordered, and thus do not interfere with the overall structure.  After seven residues, however, the capping α-helix structure is disrupted, leading to an unstable or unformed chromophore.  The &amp;lt;scene name=&#039;Green_Fluorescent_Protein/Amino_terminus/2&#039;&amp;gt;amino terminus&amp;lt;/scene&amp;gt; is less understood, but the same principle still applies even though the β-barrel does not begin until residue ten or eleven.&amp;lt;ref name=&amp;quot;Yang&amp;quot; /&amp;gt;  &lt;br /&gt;
&lt;br /&gt;
Point mutations have also been extensively studied in order to examine their effects on the chromophore.  In general, most point mutations lead to a diminished excitation, especially in regions of the sequence adjacent to the fluorophore or those that interact with the fluorophore.  An exception to this trend is the Ser&amp;lt;sup&amp;gt;65&amp;lt;/sup&amp;gt;Thr&amp;lt;sup&amp;gt;66&amp;lt;/sup&amp;gt; mutant (normal Ser&amp;lt;sup&amp;gt;65&amp;lt;/sup&amp;gt;Tyr&amp;lt;sup&amp;gt;66&amp;lt;/sup&amp;gt;), which actually increases fluorescence intensity, although the reason is unclear.&amp;lt;ref name=&amp;quot;Yang&amp;quot; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
An interesting mutation discovered by Ormo et al. (1996) was the Thr&amp;lt;sup&amp;gt;65&amp;lt;/sup&amp;gt;Tyr&amp;lt;sup&amp;gt;66&amp;lt;/sup&amp;gt;Gly&amp;lt;sup&amp;gt;67&amp;lt;/sup&amp;gt; mutant, which produces an α-helical conformation in the chromophore opposed to the normal conformation, which is nearly perpendicular to the helical axis, due to its interaction with Arg&amp;lt;sup&amp;gt;96&amp;lt;/sup&amp;gt;.  This further supports the idea that Arg&amp;lt;sup&amp;gt;96&amp;lt;/sup&amp;gt; is an important factor in the structural arrangement required for cyclization, perhaps by promoting the attack of Gly&amp;lt;sup&amp;gt;67&amp;lt;/sup&amp;gt; on the carbonyl carbon of Thr&amp;lt;sup&amp;gt;65&amp;lt;/sup&amp;gt;.&amp;lt;ref name=&amp;quot;Ormo&amp;quot; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
In high protein concentrations, GFP has been found to dimerize under the influence of high ionic strength between the two monomers.  In &#039;&#039;Aequorea victoria&#039;&#039;, the aequorin is able to bind to the &amp;lt;scene name=&#039;Green_Fluorescent_Protein/1gfl/1&#039; &amp;gt;dimer&amp;lt;/scene&amp;gt; ([[1gfl]]), but not the monomer.  Therefore, dimerization is a very important structural feature in terms of its function, as it also assists the GFP to absorb energy at the excitation wavelength of aequorin even though GFP has only a “modest” extinction coefficient.  As a result, dimers, and often even higher &amp;lt;scene name=&#039;Green_Fluorescent_Protein/1w7s/1&#039;&amp;gt;multimers&amp;lt;/scene&amp;gt; ([[1w7s]]), are predominant protein populations within the jellyfish.&amp;lt;ref name=&amp;quot;Cubitt&amp;quot;&amp;gt;[http://www.sciencedirect.com/science?_ob=ArticleURL&amp;amp;_udi=B6TCV-40W0TN7-50&amp;amp;_user=4187488&amp;amp;_coverDate=11%2F30%2F1995&amp;amp;_rdoc=1&amp;amp;_fmt=high&amp;amp;_orig=search&amp;amp;_sort=d&amp;amp;_docanchor=&amp;amp;view=c&amp;amp;_acct=C000062504&amp;amp;_version=1&amp;amp;_urlVersion=0&amp;amp;_userid=4187488&amp;amp;md5=e92730038bb92b1dfbd4af45a0283cce],Cubitt AB, Heim R, Adams SR, Boyd AE, Gross LA, Tsien R.  1995.  Understanding, improving, and using green fluorescent protein.  Trends in Biochemical Sciences.  20(11): 448-455.  DOI 0.1016/S0968-0004(00)89099-4.&amp;lt;/ref&amp;gt; &lt;br /&gt;
&lt;br /&gt;
{{Link Toggle FancyCartoonHighQualityView}}.&lt;br /&gt;
&lt;br /&gt;
== Using GFP as a Research Tool ==&lt;br /&gt;
&lt;br /&gt;
A description of some of the ways GFP is being used as a tool in research is at [[Green_Fluorescent_Protein:_Research_Tool]].&lt;br /&gt;
&lt;br /&gt;
==3D Printed Physical Model of Green Fluorescent Protein (GFP)==&lt;br /&gt;
&lt;br /&gt;
Shown below are 3D printed physical models of the Green Fluorescent Protein (GFP). The first alpha carbon backbone model is colored by three-strand repeats, including red, blue, purple, and yellow.  The second alpha carbon backbone model is colored by secondary structure, with alpha helices red and beta sheets yellow. Both models show the fluorophore molecule at the center of the GFP structure.&lt;br /&gt;
&lt;br /&gt;
[[Image:gfp1_centerForBioMolecularModeling.jpg | 550px]]&lt;br /&gt;
[[Image:gfp2_centerForBioMolecularModeling.jpg | 550px]]&lt;br /&gt;
&lt;br /&gt;
====The MSOE Center for BioMolecular Modeling====&lt;br /&gt;
&lt;br /&gt;
[[Image:CbmUniversityLogo.jpg | left | 150px]]&lt;br /&gt;
&lt;br /&gt;
The [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling] uses 3D printing technology to create physical models of protein and molecular structures, making the invisible molecular world more tangible and comprehensible. To view more protein structure models, visit our [http://cbm.msoe.edu/educationalmedia/modelgallery/ Model Gallery].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==3D structures of Green Fluorescent Protein ==&lt;br /&gt;
[[Green Fluorescent Protein 3D structures]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Reference for this Structure==&lt;br /&gt;
&lt;br /&gt;
Ormo M, Cubitt AB, Kallio K, Gross LA, Tsien RY, Remington SJ.  1996.  Crystal structure of the &#039;&#039;Aequorea victoria&#039;&#039; green fluorescent protein.  Science.  273(5280):1392-1395.  [http://www.sciencemag.org/cgi/content/abstract/273/5280/1392 DOI 10.1126/science.273.5280.1392].&lt;br /&gt;
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==References==&lt;br /&gt;
&lt;br /&gt;
{{Reflist}}&lt;br /&gt;
&lt;br /&gt;
==Additional Resources==&lt;br /&gt;
*For additional information, see: [[Colored &amp;amp; Bioluminescent Proteins]]&lt;br /&gt;
*[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1ema First Glance]&lt;br /&gt;
*PDBsum: [http://www.ebi.ac.uk/pdbsum/1ema 1ema]&lt;br /&gt;
*RCSB PDB [http://www.rcsb.org/pdb/explore.do?structureId=1ema 1ema]&lt;br /&gt;
*[http://oca.weizmann.ac.il/oca-bin/ocaids?id=1ema OCA]&lt;br /&gt;
*UniProt: [http://www.uniprot.org/uniprot/P42212 P42212]&lt;br /&gt;
*Scop: [http://scop.mrc-lmb.cam.ac.uk/scop/data/scop.b.e.gc.b.b.b.html P42212]&lt;br /&gt;
*CATH: [http://www.cathdb.info/domain/1emaA00 1emaA00]&lt;br /&gt;
*Pfam: [http://pfam.sanger.ac.uk/family?acc=PF01353 PF01353]&lt;br /&gt;
*InterPro: [http://www.ebi.ac.uk/interpro/ISearch?query=IPR000786 IPR000786]&lt;br /&gt;
*[http://www.rcsb.org/pdb/static.do?p=education_discussion/molecule_of_the_month/pdb42_1.html GFP featured] at the &#039;&#039;&#039;[http://www.rcsb.org/pdb/static.do?p=education_discussion/molecule_of_the_month/index.html Molecule of the Month]&#039;&#039;&#039; series of tutorials by [[User:David_S._Goodsell|David Goodsell]].&lt;br /&gt;
* [http://www.nature.com/nature/journal/v462/n7270/edsumm/e091112-05.html Inside green fluorescent protein] - editor&#039;s summary that accompanied [http://www.nature.com/nature/journal/v462/n7270/covers/ structural detail of GFP chromophore on the cover] of Nature.&lt;br /&gt;
&lt;br /&gt;
[[he:GFP_(Hebrew)]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Topic Page]]&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=File:Anthrax-toxin.gif&amp;diff=4395850</id>
		<title>File:Anthrax-toxin.gif</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=File:Anthrax-toxin.gif&amp;diff=4395850"/>
		<updated>2025-11-28T14:24:30Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==3D Printed Physical Model of the Anthrax Toxin Protein==&lt;br /&gt;
&lt;br /&gt;
Shown below are 3D printed physical models of the Anthrax Toxin Protein, based on the structure [http://proteopedia.org/wiki/index.php/1acc 1acc.pdb]. The full septamer model is shown in spacefill format and is colored by domain, with a single monomer shown in white. The alpha carbon backbone model is similarly colored by chain, with additional key side chains included.&lt;br /&gt;
&lt;br /&gt;
[[Image:anthrax1_centerForBioMolecularModeling.jpg|550px]]&lt;br /&gt;
[[Image:anthrax2_centerForBioMolecularModeling.jpg|550px]]&lt;br /&gt;
&lt;br /&gt;
====The MSOE Center for BioMolecular Modeling====&lt;br /&gt;
&lt;br /&gt;
[[Image:CbmUniversityLogo.jpg | left | 150px]]&lt;br /&gt;
&lt;br /&gt;
The [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling] uses 3D printing technology to create physical models of protein and molecular structures, making the invisible molecular world more tangible and comprehensible. To view more protein structure models, visit our [http://cbm.msoe.edu/educationalmedia/modelgallery/ Model Gallery].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Summary ==&lt;br /&gt;
http://www.rcsb.org/pdb/education_discussion/molecule_of_the_month/images/anthrax-toxin.gif&lt;br /&gt;
== Licensing ==&lt;br /&gt;
{{subst:No license from license selector|Don&#039;t know}}&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Emily_Ellis/Sandbox&amp;diff=4395849</id>
		<title>Emily Ellis/Sandbox</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Emily_Ellis/Sandbox&amp;diff=4395849"/>
		<updated>2025-11-28T14:23:49Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Two 3D printed objects and a box==&lt;br /&gt;
&lt;br /&gt;
&amp;lt;qt&amp;gt;file=Image:salbutamol.mp4|autoplay=false|width=600|height=460|controller=true|loop=false&amp;lt;/qt&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==A drug and its mirror image==&lt;br /&gt;
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Are the molecules shown on the left below and on the right identical, or are they different from each other? You can rotate the molecule on the right with your mouse to match the molecule on the left. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;StructureSection size=&#039;340&#039; side=&#039;right&#039; scene=&#039;61/611451/Mirror_image/2&#039;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:Salbutamol.gif]]&lt;br /&gt;
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It turns out that some molecules, such as the drug salbutamol we are using as an example here, are different from their mirror image. The left image shows the actual drug, while the browser on the right shows its mirror image. If you click on the &amp;lt;scene name=&#039;61/611451/Salbutamol/5&#039;&amp;gt;green link&amp;lt;/scene&amp;gt;, we&#039;ll show the actual drug in the browser as well, and you can rotate it with the mouse to show how they match.&lt;br /&gt;
&lt;br /&gt;
So far we focused on the shape of the molecule. To fully understand how salbutamol binds, we should show you what atoms it is made of. If you click on the &amp;quot;Show the atoms&amp;quot; link below, carbon atoms will appear in gray, oxygen atoms in red, and nitrogen atoms in blue. The molecule also contains hydrogen atoms, but these are much smaller and are not shown.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;jmol&amp;gt;&lt;br /&gt;
 &amp;lt;jmolLink&amp;gt;&lt;br /&gt;
  &amp;lt;script&amp;gt; select 601:B; color CPK; spacefill 23%; var a = [300,250,200,170,140,120,100]; for(var i IN a) {wireframe @i; delay 0.4;}&lt;br /&gt;
  &amp;lt;/script&amp;gt;&lt;br /&gt;
  &amp;lt;text&amp;gt;Show the atoms &amp;lt;/text&amp;gt;&lt;br /&gt;
 &amp;lt;/jmolLink&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;What about the box?&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
[[Image:SalbutamolBox.jpg|200px]]&lt;br /&gt;
&lt;br /&gt;
When salbutamol acts in the body, it does so by binding to a receptor in the cell membrane. Receptors help to communicate between the outside of the cell and the inside of the cell, much like a window or a door bell helps people in a house learn about what is going on outside. The receptor salbutamol binds to is a protein called the &amp;lt;scene name=&#039;61/611451/Adrenergic_receptor/6&#039;&amp;gt;adrenergic receptor&amp;lt;/scene&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
It&#039;s a big molecule, and salbutamol is difficult to see because it is surrounded by the receptor, especially if we show &amp;lt;scene name=&#039;61/611451/Adrenergic_receptor/7&#039;&amp;gt;all the atoms&amp;lt;/scene&amp;gt;. Use the links below to &amp;quot;shave away&amp;quot; parts of the molecule for a better look inside&lt;br /&gt;
&lt;br /&gt;
*&amp;lt;jmol&amp;gt;&lt;br /&gt;
 &amp;lt;jmolLink&amp;gt;&lt;br /&gt;
  &amp;lt;script&amp;gt; slab on; depth 40; var a = [80,70,60,55,53,52]; for(var i IN a) {slab @i; delay 0.4;}&lt;br /&gt;
  &amp;lt;/script&amp;gt;&lt;br /&gt;
  &amp;lt;text&amp;gt;Shave away&amp;lt;/text&amp;gt;&lt;br /&gt;
 &amp;lt;/jmolLink&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
*&amp;lt;jmol&amp;gt;&lt;br /&gt;
 &amp;lt;jmolLink&amp;gt;&lt;br /&gt;
  &amp;lt;script&amp;gt; slab on; depth 40; var a = [53,55,60,70,80,100]; for(var i IN a) {slab @i; delay 0.4;}&lt;br /&gt;
  &amp;lt;/script&amp;gt;&lt;br /&gt;
  &amp;lt;text&amp;gt;Put everything back&amp;lt;/text&amp;gt;&lt;br /&gt;
 &amp;lt;/jmolLink&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
The next scene shows salbutamol in red, and those parts of the receptor that surround it, called its binding site, in blue. Compare the blue parts to the box in the movie. It helps to use the &amp;quot;shave away&amp;quot; buttons above, and to rotate the view so it matches the view of the molecule in the movie.&lt;br /&gt;
&lt;br /&gt;
With all those blue atoms, it becomes difficult to see the salbutamol. For the 3D printed model, we shaved away the binding site (blue box), but kept the entire salbutamol, so it sticks out of the box. In the browser, we can switch the receptor atoms to a smaller radius, connecting the atoms that are bonded, to give a better view of the &amp;lt;scene name=&#039;61/611451/Adrenergic_receptor/5&#039;&amp;gt;binding site&amp;lt;/scene&amp;gt;. Again, you can use the &amp;quot;shave away&amp;quot; buttons to help seeing the red molecule inside the blue binding site.&lt;br /&gt;
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&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
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&lt;br /&gt;
&lt;br /&gt;
==Medical Uses==&lt;br /&gt;
The drug Salbutamol is an asthma drug used to treat chronic bronchitis, COPD (chronic obstructive pulmonary disorder), and exercise-induced asthma.  It is also known as Albuterol, Levalbuterol, and Proventil.  It is generally an oral inhaler that is used for prevention and treatment of the symptoms that accompany the conditions mentioned before.  &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
The drug itself is a racemic mixture, or combination of both the S-isomer (the mirror image) and the R-isomer (the drug).  The R-isomer is 150 times more likely to bond with the beta2-adrenergic receptor than the S-isomer, but it is much less expensive for the drug companies to produce both isomers when creating the drugs.  The beta2-adrenergic receptors (usually pulmonary) are 29 times more receptive to the Salbutamol than the beta1-adrenergic receptors, which are usually found in the heart. &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Some common brand names for the drug are: Aerolin, ProAir, and Ventolin.  &lt;br /&gt;
&lt;br /&gt;
&amp;lt;br&amp;gt;&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Hemoglobin&amp;diff=4395848</id>
		<title>Hemoglobin</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Hemoglobin&amp;diff=4395848"/>
		<updated>2025-11-28T14:23:03Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;StructureSection load=&#039;1gzx&#039; size=&#039;350&#039; side=&#039;right&#039; caption=&amp;quot;Human Hemoglobin α chain (grey and pink) β chain (green and yellow) with bound O2 [[1gzx]]&amp;quot; scene=&amp;quot;Hemoglobin/Foursubunits/5&amp;quot; &amp;gt;&lt;br /&gt;
== Function ==&lt;br /&gt;
&#039;&#039;&#039;Hemoglobin&#039;&#039;&#039; is an oxygen-transport protein.  Hemoglobin is an allosteric protein.  It is a &amp;lt;jmol&amp;gt;&lt;br /&gt;
  &amp;lt;jmolLink&amp;gt;&lt;br /&gt;
    &amp;lt;script&amp;gt; script /scripts/32/32/Subunits_1hho/1.spt; &lt;br /&gt;
             center visible;&amp;lt;/script&amp;gt;&lt;br /&gt;
    &amp;lt;text&amp;gt;tetramer&amp;lt;/text&amp;gt;&lt;br /&gt;
  &amp;lt;/jmolLink&amp;gt;&lt;br /&gt;
&amp;lt;/jmol&amp;gt; composed of two types of subunits designated α and β, with stoichiometry &amp;lt;scene name=&#039;Hemoglobin/Alpha2beta2/7&#039;&amp;gt;alpha2-beta2&amp;lt;/scene&amp;gt;. The  &amp;lt;scene name=&#039;Hemoglobin/Foursubunits/5&#039;&amp;gt;four subunits&amp;lt;/scene&amp;gt; of hemoglobin sit roughly at the corners of a tetrahedron, facing each other across a &amp;lt;scene name=&#039;Hemoglobin/Cavity/9&#039;&amp;gt;cavity&amp;lt;/scene&amp;gt; at the center of the molecule. Each of the subunits &amp;lt;scene name=&#039;Hemoglobin/Bbsubunitswithheme/5&#039;&amp;gt;contains a heme&amp;lt;/scene&amp;gt; prosthetic group. The &amp;lt;scene name=&#039;Hemoglobin/4heme/3&#039;&amp;gt;heme molecules&amp;lt;/scene&amp;gt; give hemoglobin its red color.&lt;br /&gt;
&lt;br /&gt;
Each individual &amp;lt;scene name=&#039;Hemoglobin/Deoxyheme/8&#039;&amp;gt;heme&amp;lt;/scene&amp;gt; molecule contains one &amp;lt;scene name=&#039;Hemoglobin/Deoxyheme_fe/9&#039;&amp;gt;Fe2+&amp;lt;/scene&amp;gt; atom. In the lungs, where oxygen is abundant, an &amp;lt;scene name=&#039;Hemoglobin/Oxyheme_fe/7&#039;&amp;gt;oxygen molecule&amp;lt;/scene&amp;gt; binds to the ferrous iron atom of the heme molecule and is later released in tissues needing oxygen. The heme group binds oxygen while still attached to the &amp;lt;scene name=&#039;Hemoglobin/Oxysubunit/8&#039;&amp;gt;hemoglobin monomer&amp;lt;/scene&amp;gt;. The spacefill view of the hemoglobin polypeptide subunit with an oxygenated heme group shows how the &amp;lt;scene name=&#039;Hemoglobin/Oxysubunitsf/4&#039;&amp;gt;oxygenated heme group is held&amp;lt;/scene&amp;gt; within the polypeptide. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;scene name=&#039;Hemoglobin/Anchortrace/5&#039;&amp;gt;Anchoring of the heme&amp;lt;/scene&amp;gt; is facilitated by a histidine nitrogen that binds to the iron. A second histidine is near the bound oxygen. The &amp;quot;arms&amp;quot; (propanoate groups) of the heme are hydrophilic and face the surface of the protein while the hydrophobic portions of the heme are buried among the hydrophobic amino acids of the protein.&lt;br /&gt;
&lt;br /&gt;
Perhaps the most well-known disease caused by a mutation in the hemoglobin protein is sickle-cell anemia.  It results from a mutation of the sixth residue in the β hemoglobin monomer from &amp;lt;scene name=&#039;32/32/Hemoglobins_1hho/9&#039;&amp;gt;glutamic acid to a valine&amp;lt;/scene&amp;gt;.  This hemoglobin variant is termed &#039;hemoglobin S&#039; ([[2hbs]]).&lt;br /&gt;
*&#039;&#039;&#039;mini hemoglobin&#039;&#039;&#039; found in neural tissue and contains 109 residues&amp;lt;ref&amp;gt;PMID:9642264&amp;lt;/ref&amp;gt; .&lt;br /&gt;
*&#039;&#039;&#039;giant hemoglobin&#039;&#039;&#039; are sulfur-binding 400kDa hemoglobin found in mouthless and gutless marine animals which get their nutrition by symbiosis with sulfur-oxidizing bacteria&amp;lt;ref&amp;gt;PMID:16204001&amp;lt;/ref&amp;gt; .&lt;br /&gt;
*&#039;&#039;&#039;truncated hemoglobin&#039;&#039;&#039; found in bacteria and plants.  They are 20-40 residues shorter than other Hb and have 2-on-2 alpha helical sandwich structure vs the 3-on-3 of other Hbs&amp;lt;ref&amp;gt;PMID:11696555&amp;lt;/ref&amp;gt; .&lt;br /&gt;
*&#039;&#039;&#039;methemoglobin&#039;&#039;&#039; contains Fe+3 rather than Fe+2 can cause the lethal disease methemoglobinemia&amp;lt;ref&amp;gt;PMID:30726002&amp;lt;/ref&amp;gt; .&lt;br /&gt;
*&#039;&#039;&#039;leghemoglobin&#039;&#039;&#039; found in roots of legumes&amp;lt;ref&amp;gt;PMID:29642729&amp;lt;/ref&amp;gt; .&lt;br /&gt;
*&#039;&#039;&#039;flavohemoglobin&#039;&#039;&#039; is flavin-binding.  It binds NO and acts in its catabolism&amp;lt;ref&amp;gt;PMID:18379989&amp;lt;/ref&amp;gt; .&lt;br /&gt;
&lt;br /&gt;
==Hemoglobin subunit binding O&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;==&lt;br /&gt;
For hemoglobin, its function as an oxygen-carrier in the blood is fundamentally linked to the equilibrium between the two main states of its quaternary structure, the unliganded &amp;quot;deoxy&amp;quot; or &amp;quot;T state&amp;quot; versus the liganded &amp;quot;oxy&amp;quot; or &amp;quot;R state&amp;quot;.  The unliganded (deoxy) form is called the &amp;quot;T&amp;quot; (for &amp;quot;tense&amp;quot;) state because it contains extra stabilizing interactions between the subunits.  In the high-affinity R-state conformation the interactions which oppose oxygen binding and stabilize the tetramer are somewhat weaker or &amp;quot;relaxed&amp;quot;.  In some organisms this difference is so pronounced that their Hb molecules dissociate into dimers in the oxygenated form.  Structural changes that occur during this transition can illuminate how such changes result in important functional properties, such as cooperativity of oxygen binding and allosteric control by pH and anions. Hemoglobin is definitely not a pure two-state system, but the T to R transition provides the major, first-level explanation of its function.&lt;br /&gt;
&lt;br /&gt;
The hemoglobin molecule (or &amp;quot;Hb&amp;quot;) is a tetramer of two α and two β chains, of 141 and 146 residues in human.  They are different but homologous, with a &amp;quot;globin fold&amp;quot; structure similar to [[myoglobin]].   &lt;br /&gt;
&lt;br /&gt;
&amp;lt;!-- &amp;lt;applet load=&#039;3hhb&#039; size=&#039;400&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Human deoxyhemoglobin (PDB code [[3hhb]])&#039;/&amp;gt; --&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Here we see a single &amp;lt;scene name=&#039;Hemoglobin/3hhb_chaina_rainbow/4&#039;&amp;gt;α chain&amp;lt;/scene&amp;gt; of hemoglobin, starting with an overview of the subunit.  The 6 major and 2 short α-helices that make up the structure of a Hb subunit (the &amp;quot;globin fold&amp;quot;) are &amp;lt;scene name=&#039;Hemoglobin/3hhb_chaina_heliceslabeled/4&#039;&amp;gt;labeled A through H&amp;lt;/scene&amp;gt;, which is the traditional naming scheme.  For example, the proximal histidine (the tightest protein Fe ligand) is often called &amp;lt;scene name=&#039;32/32/Hisf9/1&#039;&amp;gt;His F9&amp;lt;/scene&amp;gt;, since it is residue 9 on helix F (it is residue 87 in the human α chain).  The helices form an approximately-cylindrical bundle, with the heme and its central Fe atom bound in a &amp;lt;scene name=&#039;Hemoglobin/3hhb_chaina_efpocket/4&#039;&amp;gt;hydrophobic pocket between the E and F helices&amp;lt;/scene&amp;gt;.  &lt;br /&gt;
&lt;br /&gt;
&amp;lt;scene name=&#039;32/32/Cv/2&#039;&amp;gt;In the present animation scene&amp;lt;/scene&amp;gt; the &amp;lt;span style=&amp;quot;color:pink;background-color:black;font-weight:bold;&amp;quot;&amp;gt;oxy (in pink)&amp;lt;/span&amp;gt; and &amp;lt;span style=&amp;quot;color:deepskyblue;background-color:black;font-weight:bold;&amp;quot;&amp;gt;deoxy (in deepskyblue)&amp;lt;/span&amp;gt; α1 heme groups were superimposed on each other, to give a local comparison at this site, a closeup around the heme O2-binding site.  The heme is quite domed in the &amp;lt;span style=&amp;quot;color:deepskyblue;background-color:black;font-weight:bold;&amp;quot;&amp;gt;deepskyblue T-state (deoxy) form&amp;lt;/span&amp;gt;, with the 5-coordinate, high-spin &amp;lt;span style=&amp;quot;color:orange;background-color:black;font-weight:bold;&amp;quot;&amp;gt;Fe (orange ball)&amp;lt;/span&amp;gt; out of the plane.  In the &amp;lt;span style=&amp;quot;color:pink;background-color:black;font-weight:bold;&amp;quot;&amp;gt;pink R-state form&amp;lt;/span&amp;gt; a CO molecule is bound at the right &amp;lt;span style=&amp;quot;color:lime;background-color:black;font-weight:bold;&amp;quot;&amp;gt;(C in green&amp;lt;/span&amp;gt;,&amp;lt;font color=&#039;red&#039;&amp;gt;&amp;lt;b&amp;gt;O in red&amp;lt;/b&amp;gt;&amp;lt;/font&amp;gt;); the Fe, now 6-coordinate low-spin, has moved into the heme plane, which has flattenened.  The proximal His (at left) connects the Fe to helices on the proximal side, making the Fe position sensitive to changes in the globin structure and vice versa.  Remember that this scene shows a subunit in the all-unliganded versus the all-liganded states of Hb; when oxygen binds to just one subunit, then its internal structure undergoes some but not all of these changes, depending on conditions.   &amp;lt;jmol&amp;gt;&amp;lt;jmolButton&amp;gt;&lt;br /&gt;
&amp;lt;script&amp;gt;if (_animating); anim pause;set echo bottom left; color echo white; font echo 20 sansserif;echo Animation Paused; else; anim resume; set echo off;endif;&amp;lt;/script&amp;gt;&lt;br /&gt;
&amp;lt;text&amp;gt;Toggle Animation&amp;lt;/text&amp;gt;&lt;br /&gt;
&amp;lt;/jmolButton&amp;gt;&amp;lt;/jmol&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;!-- kinemage not supported&lt;br /&gt;
{|&lt;br /&gt;
|&amp;lt;kinemage align=&amp;quot;left&amp;quot; width=&amp;quot;420&amp;quot; height=&amp;quot;300&amp;quot; file=&amp;quot;HbAllo.kin&amp;quot;/&amp;gt;&lt;br /&gt;
|}&lt;br /&gt;
--&amp;gt;&lt;br /&gt;
O&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; binds in the same place as CO, with similar effects on the structure; however, for O2 the outer atom is angled rather than straight.  The equilibrium between free and bound O&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; is very rapid, with on and off rates that are sensitive to protein conformation.  Both CO and NO dissociate from the Fe atom very slowly, so that these gases act as respiratory poisons.  The α and β chains differ somewhat in their rates and relative affinities for O&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; and other ligands, by virtue of heme-pocket differences, but the differences between affinities in the R vs T quaternary states are much larger.&lt;br /&gt;
&lt;br /&gt;
Both α and β chains of Hb resemble [[myoglobin]] (the single-chain O2-binder in muscle), both in overall tertiary structure and in using an Fe atom centered in a heme group as the site where oxygen is reversibly bound.  The heme is surrounded by a hydrophobic pocket, which is necessary in order for it to bind oxygen reversibly without undergoing oxidation or other undesirable reactions.  &lt;br /&gt;
&lt;br /&gt;
The heme binding pocket contains mostly &amp;lt;scene name=&#039;32/32/Heme_binding_pocket_apo/1&#039;&amp;gt;hydrophobic residues&amp;lt;/scene&amp;gt;, shown in grey. They actually surround the binding site so thoroughly that O2 cannot get in or out without parts of the protein moving out of the way a bit, so that its dynamic properties are essential to have any O2 binding at all; this restrictive process also increases the specificity of ligand binding.&lt;br /&gt;
&lt;br /&gt;
The shift between R and T state requires subunit interactions and does not occur in myoglobin, or in isolated α or β chain monomers.  These monomers bind O2 quite tightly, which would work well for loading O2 in the lungs but would not allow unloading it for delivery to the tissues.  Therefore, the central critical feature of hemoglobin function is how it achieves, uses, and allosterically controls cooperativity between the 4 binding sites in the tetramer to tune O2 binding for satisfying physiological needs.&lt;br /&gt;
&lt;br /&gt;
Linkage of the heme Fe through the proximal His results in tertiary-structure changes that can then transmit their effects to other subunits in the tetrameric assemblage.  This allows O2 binding in one subunit to indirectly affect the affinitiy of other subunits.  Briefly, inside the α chains the R/T equilibrium is reflected in changes in Fe spin state and position as it moves in or out of the heme plane; the proximal His changes distance and angle relative to the heme; the F helix shifts; Tyr 140 moves and its H-bond to backbone weakens; and both the C-terminus of the chain and Arg 141 move significantly at the interface.  These movements are animated at this [[User:Jaime_Prilusky/How_do_we_get_the_oxygen_we_breathe|page]].  Changes at the subunit interface (coupled with changes at the Fe, as we have seen) alter the equilibrium between the deoxy and oxy quaternary structures, and conversely a change of quaternary structure alters the balance between the two states inside a given subunit.  Each O2 that binds increases the likelihood of switching the tetramer into the oxy state, and once it switches, the O2 affinity at all sites increases because the local structure changes have either already occurred or are easier to make.&lt;br /&gt;
&lt;br /&gt;
Click here to show the α1 subunit, but centered for the whole tetramer.&lt;br /&gt;
&lt;br /&gt;
==The Hb tetramer T -&amp;gt; R transition==&lt;br /&gt;
&lt;br /&gt;
The central cavity, is wider in the deoxy state, forming phosphate sites;  quaternary structure change as rigid rotations of α-β dimers;  α1-β2 contact overview;  &amp;quot;ratchet&amp;quot; vs &amp;quot;hinge&amp;quot; at the a1b2 interface;  α1-α2 salt bridges;  charged groups at the C-terminus of β2 which stabilize the deoxy form;  and finally a summary overview.  (from PDB files bio3HHB and bio1HCO)&lt;br /&gt;
&lt;br /&gt;
Look down one of the approximate 2-fold axes, with α subunits at the top and β subunits at the bottom.  Notice that the hemes are quite far apart, so that their interactions must be mediated by the protein.&lt;br /&gt;
For a view down the exact crystallographic 2-fold axis from the β1- β2 end, click here: The yellowtint crosses are phosphate sites present in deoxy but not oxy Hb. In oxy Hb, the β subunits move closer together, squeezing out phosphates (such as 2,3 DPG), and allowing the N- and C-termini to interact.  DPG and other phosphates bind much more strongly to the deoxy quaternary structure;  therefore they necessarily push the equilibrium toward deoxy Hb, and because of that they decrease O2 affinity.  Such regulatory phosphate molecules are useful in the blood, because their concentrations can be controlled to shift the Hb O2-binding curve so that it is working across the steepest and most efficient part under conditions in the lungs and tissues.  For instance, at high altitude the body makes more DPG, to unload O2 more effectively in the muscles.&lt;br /&gt;
&lt;br /&gt;
Like the [[PFK]], to the first approximation the Hb molecule consists of two &amp;quot;dimers&amp;quot; (α1-β1 and α2-β2), which rotate relative to each other as rigid bodies in the R-T transition.  The α1-β1 unit undergoes relatively little internal rearrangement, but its overall rotation with respect to the α2-β2 unit is considerable.  The net rotation of the two dimers alters their interactions with one another, most notably at the allosteric effector site between β1 and β2 (PO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt; binding) and at the important α1-β2 interface, where mutations have the largest effect on Hb allosteric properties.  Although the symmetry is not exact, similar parts of the subunits contact each other:  the C helix, and the &amp;quot;FG corner&amp;quot; between helices F and G.&lt;br /&gt;
&lt;br /&gt;
Have a look at a closeup that emphasizes the ratchet contact between the C helix of α1 and the FG corner of β2;  His 97 of the β2 FG corner makes a large jump against Thr 38 and Thr 41 of the α1 C helix.  In a closeup of the hinge contact, the motions are mainly rotations without much shift, between the α1 FG corner and the β2 C helix.  Labels help identify these parts.  Since this is a complex motion orchestrated between the fit of two quite different sets of contacts in the two states, this interface is critical to making Hb allostery work, and mutations of residues in this interface have been found to be especially likely to influence cooperativity and allostery.&lt;br /&gt;
&lt;br /&gt;
There are salt links between α1 and α2, which stabilize the deoxy form.  Here’s an overview down the exact 2-fold axis between the subunits, showing that there are two equivalent sets of interactions, on either side of the twofold.&lt;br /&gt;
&lt;br /&gt;
Salt links at the C-terminus of β2 stabilize the deoxy T form and make a large contribution to the pH dependence of Hb oxygen binding, known as the Bohr Effect.  In the making and breaking of these interactions, His β 146 moves a great deal, disrupting the salt link (charged H-bond) to Asp β 94 that is formed in the T state.  Since His titrates near physiological pH, this interaction is quite pH sensitive.  At low pH, when more protons are present, the His ring N is more likely to be protonated and positive; this strengthens its H-bond with Asp 94, thus favoring the T state and decreasing O2 affinity.  The pH effect, or Bohr Effect, can be considered as allosteric regulation by the binding of protons.  It is important biologically, because it promotes oxygen unloading in the tissues where proton concentrations are elevated, for instance by the production of lactic acid in muscle.&lt;br /&gt;
&lt;br /&gt;
==Truncated hemoglobins==&lt;br /&gt;
see [[Journal:JBIC:8]]&lt;br /&gt;
&lt;br /&gt;
==3D Printed Physical Model of Hemoglobin at The MSOE Center for BioMolecular Modeling==&lt;br /&gt;
&lt;br /&gt;
[[Image:CbmUniversityLogo.jpg | left | 150px]]&lt;br /&gt;
&lt;br /&gt;
Shown below is a 3D printed physical model of Hemoglobin, based on the structure [http://proteopedia.org/wiki/index.php/1a3n 1a3n.pdb]. The two alpha-globin chains are colored light red, the two beta globin chains are colored dark red, and the four heme groups are colored yellow. It has been designed with precisely embedded magnets that allow the four chains to pull apart into individual pieces.&lt;br /&gt;
&lt;br /&gt;
[[Image:Cbm_hemoglobin1.jpg|450px]]&lt;br /&gt;
[[Image:Cbm_hemoglobin2.jpg|550px]]&lt;br /&gt;
[[Category:3D printer files]] &lt;br /&gt;
==Additional Resources==&lt;br /&gt;
*[[Tutorial:How do we get the oxygen we breathe]]&lt;br /&gt;
*Hemoglobin structure tutorial at [http://molviz.org MolviZ.Org]. Includes smooth animations of deoxy↔oxy transitions (morphs), a 16-molecule polymer of sickle hemoglobin&lt;br /&gt;
*[[User:Eric Martz/Hemoglobin Quiz|Practice Hemoglobin Quiz]] (immediate feedback)&lt;br /&gt;
*[[Ann Taylor/Hemoglobin]]&lt;br /&gt;
*[[Glycated hemoglobin]]&lt;br /&gt;
*[[Molecular Playground/Hemoglobin-Haptoglobin Complex]]&lt;br /&gt;
*[http://hemoglobin.molviz.org Hemoglobin Molecular Structure] including smooth animations of deoxy&amp;amp;harr;oxy transitions (morphs) and a 16-molecule polymer of sickle hemoglobin.&lt;br /&gt;
*[[Porphyrin]]&lt;br /&gt;
*[[Student Projects for UMass Chemistry 423 Spring 2012-8]]&lt;br /&gt;
*[[Hemoglobin (Hebrew)]]&lt;br /&gt;
&lt;br /&gt;
==Hemoglobin 3D structures==&lt;br /&gt;
See [[Hemoglobin 3D structures]].&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References, for further information on Hemoglobin==&lt;br /&gt;
&#039;&#039;&#039;To the structures used here:&#039;&#039;&#039;&lt;br /&gt;
*Baldwin (1980) &amp;quot;The crystal structure of human carbonmonoxy haemoglobin at 2.7A resolution&amp;quot;, J. Mol. Biol. 136: 103.  ([[1hco]]) [http://www.ncbi.nlm.nih.gov/pubmed/7373648 PMID: 7373648]&lt;br /&gt;
*Fermi, Perutz, Shaanan, &amp;amp; Fourme (1984) &amp;quot;The crystal structure of human deoxy haemoglobin at 1.74A resolution&amp;quot;, J. Mol. Biol. 175: 159.  ([[3hhb]])&lt;br /&gt;
*Jotaro Igarashi, Kazuo Kobayashi and Ariki Matsuoka (2011) &amp;quot;A hydrogen-bonding network formed by the B10-E7-E11 residues of a truncated hemoglobin from Tetrahymena pyriformis is critical for stability of bound oxygen and nitric oxide detoxification&amp;quot;, J. Biol. Inorg. Chem. 16(4):599-609 ([[3aq9]]) [http://www.ncbi.nlm.nih.gov/pubmed/21298303 PMID: 21298303]&lt;br /&gt;
 &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;General treatments of Hb allostery:&#039;&#039;&#039;&lt;br /&gt;
*Perutz (1970) &amp;quot;Stereochemistry of cooperative effects in haemoglobin&amp;quot;, Nature 228: 726&lt;br /&gt;
*Baldwin &amp;amp; Chothia (1979) &amp;quot;Haemoglobin.  The structural changes related to ligand binding and its allosteric mechanism&amp;quot;, J. Mol. Biol. 129: 175. [http://www.nature.com/nature/journal/v228/n5273/abs/228726a0.html link]&lt;br /&gt;
*Dickerson &amp;amp; Geis (1983) &amp;quot;Hemoglobin: Structure, Function, and Pathology&amp;quot;, Benjamin/Cummings Publ., Menlo Park, CA&lt;br /&gt;
*Perutz (1989) &amp;quot;Mechanisms of cooperativity and allosteric regulation in proteins&amp;quot;, Quarterly Rev. of Biophys. 22: 139-236&lt;br /&gt;
*Ackers, Doyle, Myers, &amp;amp; Daugherty (1992) &amp;quot;Molecular code for cooperativity in hemoglobin&amp;quot;, Science 255: 54&lt;br /&gt;
*Perutz, Fermi, Poyart, Pagnier, &amp;amp; Kister (1993) &amp;quot;A novel allosteric mechanism in haemoglobin:  Structure of bovine deoxyhaemoglobin, absence of specific chloride binding sites, and origin of the chloride-linked Bohr Effect in bovine and human haemoglobin&amp;quot;, J. Mol. Biol. 233: 536&lt;br /&gt;
&#039;&#039;&#039;Hb structures in other quaternary states or intermediates:&#039;&#039;&#039;&lt;br /&gt;
*Silva, Rogers, &amp;amp; Arnone (1992) &amp;quot;A third quaternary structure of human hemoglobin A at 1.7A resolution&amp;quot;, J. Biol. Chem. 267: 17248&lt;br /&gt;
*Smith, Lattman, &amp;amp; Carter (1991) &amp;quot;The mutation β99 Asp-Tyr stabilizes Y - A new, composite quaternary state of human hemoglobin&amp;quot;, Proteins: Struct., Funct., Genet. 10: 81&lt;br /&gt;
*Liddington, Derewenda, Dodson, Hubbard, &amp;amp; Dodson (1992) &amp;quot;High resolution crystal structures and comparisons of T state deoxyhaemoglobin and two liganded T-state haemoglobins: T(α-oxy)haemoglobin and T(met)Haemoglobin&amp;quot;, J. Mol. Biol. 228: 551&lt;br /&gt;
&#039;&#039;&#039;More information on hemoglobin&#039;&#039;&#039;&lt;br /&gt;
*Perutz, M.F. (1978) Hemoglobin Structure and Respiratory Transport, Scientific American, volume 239, number 6.&lt;br /&gt;
*Squires, J.E. (2002) Artificial Blood, Science 295, 1002.&lt;br /&gt;
*Vichinsky, E. (2002) New therapies in sickle cell disease. Lancet 24, 629.&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
{{Clear}}&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;Content Donators&#039;&#039;&#039;==&lt;br /&gt;
Currently (June 22, 2008) most all of the content of this page comes from three main sources of generously donated content.  Their work has been imported into this page.  In their order of appearance on the page:&lt;br /&gt;
# &#039;&#039;&#039;Content adapted with permission from Eric Martz&#039;s hemoglobin tutorial at http://molviz.org&#039;&#039;&#039;&lt;br /&gt;
# &#039;&#039;&#039;Content adapted with permission from David S. Goodsell and Shuchismita Dutta&#039;s Molecule of the Month on Hemoglobin http://mgl.scripps.edu/people/goodsell/pdb/pdb41/pdb41_1.html&#039;&#039;&#039;&lt;br /&gt;
# &#039;&#039;&#039;Content adapted with permission from Jane S. and David C. Richardson&#039;s http://kinemage.biochem.duke.edu/&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
[[he: Hemoglobin (Hebrew)]]&lt;br /&gt;
[[Category:Topic Page]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Antibody&amp;diff=4395847</id>
		<title>Antibody</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Antibody&amp;diff=4395847"/>
		<updated>2025-11-28T14:21:38Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;StructureSection load=&#039;1hzh&#039; size=&#039;350&#039; side=&#039;right&#039; scene=&#039;&#039; caption=&#039;Glycosylated human Igg with heavy chains (red and light red), light chains (aqua and green) (PDB code [[1hzh]])&#039;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Antibodies&#039;&#039;&#039;, also known as &#039;&#039;&#039;Immunoglobulins&#039;&#039;&#039; (Ig) are gamma globulin proteins, primarily found in the blood of vertebrates.  These [[glycoproteins]] serve as a critical component of the immune system when the host fails to activate alternative compliment pathways or phagocytic cells in response to invading microorganisms or other [http://en.wikipedia.org/wiki/Antigen antigens]. The incredible specificity with which immunoglobulins bind to an antigen is based upon structural complementarity between the antigen and antibody &amp;lt;scene name=&#039;Antibody/1hzh_heavy_chains/1&#039;&amp;gt;heavy &amp;lt;/scene&amp;gt;and &amp;lt;scene name=&#039;Antibody/1hzh_light_chains/1&#039;&amp;gt;light chains &amp;lt;/scene&amp;gt;. It is this specificity that has made &amp;lt;scene name=&#039;Antibody/1hzh_starting_scene/3&#039;&amp;gt;antibodies&amp;lt;/scene&amp;gt; a critical component in laboratory and medical research. &amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;Humanized mouse antibody (hmFab)&#039;&#039;&#039; is a modified mFab which resembles more hFab.&amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;Broadly neutralizing Fab&#039;&#039;&#039; and &#039;&#039;&#039;Neutralizing Fab&#039;&#039;&#039; are anti-virus Fab. &amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;Intrabody&#039;&#039;&#039; is intracellular antibody. &amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;Sybody&#039;&#039;&#039; is synthetic nanobody (syVHH).&amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;Diabody&#039;&#039;&#039; is a recombinant bispecific antibody constructed from heterogenous single chain antibody. &amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;Lama antibodies&#039;&#039;&#039; or &#039;&#039;&#039;nanobodies&#039;&#039;&#039; or &#039;&#039;&#039;camelid&#039;&#039;&#039; or &#039;&#039;&#039;VHH&#039;&#039;&#039; are natural single-domain antibodies containing just the heavy chain.&amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;scFv&#039;&#039;&#039; is a &#039;&#039;&#039;single chain variable fragment&#039;&#039;&#039; in a fusion protein of the variable regions of the heavy and light chains of immunoglobulin. &amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;VH domain&#039;&#039;&#039; is the variable domain of the antibody heavy chain.&amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;Bispecific antibody&#039;&#039;&#039; or &#039;&#039;&#039;biparatopic antibody&#039;&#039;&#039; can bind to two epitopes of an antigen simultaneously.&amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;Polyclonal antibodies&#039;&#039;&#039; are a mixture of antibodies that bind to several epitopes of an antigen simultaneously.&amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;Ultralong antibody&#039;&#039;&#039; is found in bovine.  It has unusually long CDR H3 regions and has more effective defence against disease than typical antibodies &amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;Gluebody&#039;&#039;&#039; is a modified nanobody which produces far superior resolution of diffraction upon binding to protein.&amp;lt;br /&amp;gt;&lt;br /&gt;
*&#039;&#039;&#039;Monobody&#039;&#039;&#039; is an antibody mimic synthetic protein containing a FN3 domain of fibronectin. &amp;lt;br /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
See more in&amp;lt;br /&amp;gt;&lt;br /&gt;
[[IgA]]&amp;lt;br /&amp;gt;&lt;br /&gt;
[[IgG Branco]]&amp;lt;br /&amp;gt;&lt;br /&gt;
[[Monoclonal Antibody]].&amp;lt;br /&amp;gt;&lt;br /&gt;
For Anti-HIV-1 antibodies see [[Human Fab PG16]] and [[VRC01 gp120 complex|VRC01 and VRC01-like antibodies are important in neutralizing HIV-1]]&amp;lt;br /&amp;gt;&lt;br /&gt;
For Anti-VEGF Fab see [[Bevacizumab]] (Avastin)&amp;lt;br /&amp;gt;&lt;br /&gt;
For Anti-factor IX Fab see [[Conformation-specific anti-Factor IX antibodies]]&amp;lt;br /&amp;gt;&lt;br /&gt;
For blue luminescent Fab see [[Blue Luminescent Antibody Derived from House Mouse]]&amp;lt;br /&amp;gt;&lt;br /&gt;
For Anti-vitamin Fab see [[MR1 Binds Vitamin Metabolites]]&amp;lt;br /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:230px-B cell activation2.png|270px|left|thumb| Production of Antibodies by Plasma Cells]]&lt;br /&gt;
{{Clear}}&lt;br /&gt;
__TOC__&lt;br /&gt;
==Cellular Basis of Antibody Production==&lt;br /&gt;
When a foreign antigen binds to a B-lymphocyte ([http://en.wikipedia.org/wiki/B_cell B-cell]), it activates the B-cell, and upon stimulation by [http://en.wikipedia.org/wiki/Helper_t_cell helper T-cells], undergoes clonal proliferation and B-cell maturation into antibody forming [http://en.wikipedia.org/wiki/Plasma_cells plasma cells]. Each plasma cell is programmed to make an antibody of a single specificity, which it releases into the blood. &amp;lt;ref name=&amp;quot;Roit&amp;quot;&amp;gt; Roit, I. M. Roit&#039;s Essential Immunology. Oxford: Blackwell Science Ltd., 1997.&amp;lt;/ref&amp;gt;  Once in the blood, antibodies aid [http://en.wikipedia.org/wiki/Humoral_immune_system the humoral immune system] in three predominant ways: They coat foreign pathogens preventing them from entering healthy cells or disrupting antigen function; they coat pathogens, stimulating their removal via [http://en.wikipedia.org/wiki/Opsonization opsonization] by [http://en.wikipedia.org/wiki/Phagocytes phagocytes]; and they trigger destruction of pathogens by stimulating the [http://en.wikipedia.org/wiki/Complement_system complement pathway] or by [http://en.wikipedia.org/wiki/Antibody-dependent_cellular_cytotoxicity Antibody Dependent Cell-mediated Cytotoxicity], among other immune responses. &amp;lt;ref&amp;gt;PMID:8476565&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID:16234578&amp;lt;/ref&amp;gt; All of these functions rely heavily on accurate antigen binding and communication with other immune effector cells. The amazing specificity antibodies operate with is made possible by the physical structure of the antibody, which appears simplistic, but contains several levels of additional complexity. &lt;br /&gt;
&lt;br /&gt;
==Structure of the Immunoglobulin==&lt;br /&gt;
&amp;lt;scene name=&#039;Antibody/1igt_starting_scene/3&#039;&amp;gt;Refined Structure of an Intact IgG2a Monoclonal Antibody&amp;lt;/scene&amp;gt; ([[1igt]]).&lt;br /&gt;
&lt;br /&gt;
The basic functional unit of an antibody is an immunoglobulin monomer, but antibodies secreted from plasma cells are typically dimeric with occasional higher order structures. Typical secreted antibodies have a basic four-peptide structure of two identical &amp;lt;scene name=&#039;Antibody/1igt_heavy_chains/1&#039;&amp;gt;heavy chains &amp;lt;/scene&amp;gt;and two identical &amp;lt;scene name=&#039;Antibody/1igt_light_chains/1&#039;&amp;gt;light chains&amp;lt;/scene&amp;gt; joined together by interchain &amp;lt;scene name=&#039;Antibody/1igt_disulfide_bonds/2&#039;&amp;gt;disulfide bonds&amp;lt;/scene&amp;gt;, forming a “Y” shaped molecule. The disulfide bonds are positioned within a flexible region called the &amp;lt;scene name=&#039;Antibody/1igt_hinge_region/1&#039;&amp;gt;hinge region&amp;lt;/scene&amp;gt;, which seperates the lobes of the antibody from one another and provides ample flexibility to bind antigens effectively. &amp;lt;ref name=&amp;quot;Roit&amp;quot; /&amp;gt; Each domain (2 heavy and 2 light) contain between 70-110 amino acids and are classified into different categories according to size and function. &amp;lt;ref&amp;gt;PMID:10545762&amp;lt;/ref&amp;gt; Both domains, heavy and light, contain variable and constant regions that are crucial to antibody function. &amp;lt;ref&amp;gt;PMID:107164&amp;lt;/ref&amp;gt; &lt;br /&gt;
&lt;br /&gt;
===Heavy Chain===&lt;br /&gt;
There are five types of immunoglobulin heavy chains, in mammals, α, δ, ε, γ, and μ,  and give rise to the five unique classes or isotypes of antibodies, IgA, IgD, IgE, IgG, and IgM, which differ in size and composition. Each &amp;lt;scene name=&#039;Antibody/1igt_heavy_chains_ribbon/1&#039;&amp;gt;heavy chain &amp;lt;/scene&amp;gt;has a &amp;lt;scene name=&#039;Antibody/1igt_startconstant_region/1&#039;&amp;gt;constant region &amp;lt;/scene&amp;gt; and &amp;lt;scene name=&#039;Antibody/1igt_start_heavy_variable/1&#039;&amp;gt;variable region&amp;lt;/scene&amp;gt;. The constant region is identical in all antibodies of the same isotype, but differ in antibodies of different isotypes; i.e. all IgA have the same sequence in their heavy chain constant region, but these constant regions differ between IgA and IgD, etc. &amp;lt;ref&amp;gt;PMID:15040582&amp;lt;/ref&amp;gt; The α, δ, and γ heavy chains have a constant region composed of &amp;lt;scene name=&#039;Antibody/1igt_heavy_3_chains/1&#039;&amp;gt;three tandem immunoglobulin domains&amp;lt;/scene&amp;gt; while heavy chains ε and μ contain four. The variable region of the heavy chain in antibodies is different for all antibodies created by different B-cells. &amp;lt;ref&amp;gt;PMID:107164&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Image:New Antibody2.JPG|450px|left|thumb| Typical Structure of an Antibody]]&lt;br /&gt;
&lt;br /&gt;
===Light Chain===&lt;br /&gt;
Every antibody contains two &amp;lt;scene name=&#039;Antibody/1igt_light_chains_ribbon/1&#039;&amp;gt;light chains &amp;lt;/scene&amp;gt;that are identical to each other. There are two types of immunoglobulin light chains in mammals, labeled lambda and kappa, with only one represented in each antibody. Each light chain has one &amp;lt;scene name=&#039;Antibody/1igt_light_chains_constnat_reg/1&#039;&amp;gt;constant domain &amp;lt;/scene&amp;gt;followed by one &amp;lt;scene name=&#039;Antibody/1igt_light_chain_variable/1&#039;&amp;gt;variable domain&amp;lt;/scene&amp;gt;, with a total length of about 215 amino acids. &amp;lt;ref name=&amp;quot;Roit&amp;quot; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
=== The Regions: Fab, Fv, CDR, and Fc.===&lt;br /&gt;
The immunoglobulin can be broken down into regions, each serving a different purpose: &lt;br /&gt;
&lt;br /&gt;
====Variable Regions====&lt;br /&gt;
The &amp;lt;scene name=&#039;Antibody/1igt_fab_region/1&#039;&amp;gt;Fab region &amp;lt;/scene&amp;gt;(Fragment, Antigen Binding region) is composed of one constant and one variable domain from each heavy and light chain of the antibody. It is the part of the antibody that gives it its famous “Y” shape.&amp;lt;ref&amp;gt;PMID:9048542&amp;lt;/ref&amp;gt; Held within the Fab region is the variable domain, also known as the Fv region.&amp;lt;ref&amp;gt;PMID:4569769&amp;lt;/ref&amp;gt; Within the Fv region lie &amp;lt;scene name=&#039;Antibody/1igt_start_variable_loops/1&#039;&amp;gt;“hypervariable regions,”&amp;lt;/scene&amp;gt; positioned at one end of the variable domain where they form parts of the Beta-turn loops and are clustered close to each other in space. The clustering of the hypervariable loops at the tips of the variable regions where the antigen-binding site is located makes them perfect candidates for antigen recognition. &amp;lt;ref name=&amp;quot;Roit&amp;quot; /&amp;gt;The sequence heterogeneity of the three heavy and three light chain hypervariable loops creates significant antigen specificity diversity through variations in the binding surface nature and shape. Each hypervariable region can be viewed as an independent structure contributing to the complementarity of the biding site and antigen and is often referred to as a complementarity determining region (CDR). &amp;lt;ref&amp;gt;PMID:107164&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
====Constant Regions====&lt;br /&gt;
The remaining part of the antibody, namely the &amp;lt;scene name=&#039;Antibody/1igt_fc/2&#039;&amp;gt;Fc region&amp;lt;/scene&amp;gt;, does not play a role in binding the antigen, but rather is responsible for modulating the immune systems response to the formation of an antibody-antigen complex. The Fragment Crystallizable (Fc) region is composed of two heavy chain constant regions that are isotype specific. &amp;lt;ref&amp;gt;PMID:15040582&amp;lt;/ref&amp;gt; Antibodies are glycoproteins because of &amp;lt;scene name=&#039;Antibody/1igt_glycosylation/1&#039;&amp;gt;glycosylation &amp;lt;/scene&amp;gt;at conserved positions in their Fc regions. This glycosylation is a critical component determing the rate of antibody clearance form the body.&amp;lt;ref&amp;gt;PMID:9032990&amp;lt;/ref&amp;gt; Once an antibody binds to an antigen, the Fc region binds to Fc receptors, among other proteins, to mediate a host of different physiological responses ranging from oposonization, to degranulation of mast cells, to the release of cytokines and cytotoxic molecules, etc. resulting in the destruction of the pathogen. &amp;lt;ref&amp;gt;PMID:9052877&amp;lt;/ref&amp;gt; Depending on the class of antibody, as dictated by the identity of the Fc region, the antibody half-life and distribution throughout the body varies. Further, since Fc receptors are antibody isotype specific, the type of immune response is dependent on the type of Fc region on the immunoglobulin, allowing for different immune responses to the same pathogen if necessary.&amp;lt;ref&amp;gt;PMID:11244038&amp;lt;/ref&amp;gt; See table for brief characterization of Immunoglobulin isotypes: &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; border=&amp;quot;1&amp;quot; width=&amp;quot;70%&amp;quot; style=&amp;quot;text-align:center&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
!  colspan=&amp;quot;2&amp;quot; align=&amp;quot;center&amp;quot;| Immunoglobulin Classes and Function&lt;br /&gt;
|-&lt;br /&gt;
!  Class &lt;br /&gt;
!  Function and Oligomeric State&amp;lt;ref name=&amp;quot;Roit&amp;quot; /&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
!  IgG&lt;br /&gt;
|  Dimeric - The most abundant Ig in the extravascular fluids. Neutralizes toxins and combats microorganisms by activating the compliment system and facilitating the binding of phagocytic cells. &lt;br /&gt;
|-&lt;br /&gt;
!  [[IgA]]&lt;br /&gt;
|  Dimeric - Is the major Ig in seromucous secretions, where it serves to defend the external body surfaces.&lt;br /&gt;
|-&lt;br /&gt;
!  IgM&lt;br /&gt;
|  Pentameric – It is an intravascular antibody and is produced very early in the immune response. Due to it high oligomeric state, it is extremely effective as a bacterial agglutinator and mediator of complement-dependent cytolysis, making it a powerful first-line defense against bacterial pathogens.&lt;br /&gt;
|-&lt;br /&gt;
!  IgD&lt;br /&gt;
|  Dimeric - It is present on the lymphocyte and functions together with IgM as the antigen receptor on naïve B-cells. &lt;br /&gt;
|-&lt;br /&gt;
!  IgE&lt;br /&gt;
|  It binds to mast cells and upon contact with antigen, leads to local recruitment of antimicrobial agents via degranulation of the mast cell and release of inflammatory mediators. IgE is important for certain kinds of parasitic infections and is responsible for the symptoms of [http://en.wikipedia.org/wiki/Atopy atopic allergies] like eczema and asthma. &lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
A model of the IgG molecule is present in the figure which indicates the spatial disposition and interaction of the domains in IgG. As Dr. Ivan Roitt writes in Essential Immunolgy, “To enable the Fab arms to have the freedom to move and twist so that they can align their hypervariable regions with the antigenic sites on large immobile carriers, and to permit the Fc structures to adjust spatially in order to trigger their effector functions, it is desirable for IgG to have a high degree of flexibility. And it has just that. Structural analysis shows that the Fab can ‘elbow-bend’ at its V-C junction and twist about the hinge, which itself can more properly be described as a loose thether, allowing the Fab and the Fc to drift relative to each other with remarkable suppleness. It could be said that movements like that make it a very sexy molecule!” &amp;lt;ref name=&amp;quot;Roit&amp;quot; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:VDJ recombination.png|400px|left|thumb| Image of V(D)J Recombination]]&lt;br /&gt;
{{Clear}}&lt;br /&gt;
&amp;lt;scene name=&#039;Antibody/Rituxan_starting_scene/1&#039;&amp;gt;Crystal structure of Rituximab Fab in complex with an epitope peptide&amp;lt;/scene&amp;gt; ([[2osl]]).&lt;br /&gt;
&lt;br /&gt;
== Antibody Diversity ==&lt;br /&gt;
Considering the nearly infinite number of possible antigens that can invade the body, the immune system had to develop a method for accurately targeting each one of these compounds, ranging from small molecules, to stray proteins, to viruses capable of infecting cells. The antibody was the immune systems response to this problem. It has been estimated that humans generate about 10^10 different antigens, each capable of binding a unique epitope of an antigen. Since antibodies are proteins, and proteins are controlled by the genes from which they are transcribed, a clever system of gene shuffling and manipulations developed to enable the immune system to create a huge repertoire of antibodies from a limited number of genes. &amp;lt;ref&amp;gt;PMID:8612345&amp;lt;/ref&amp;gt; The variable region of each immunoglobulin chain is encoded in several pieces known as gene segments. For heavy chains, these segments are called the variable (V), diversity (D), and joining (J) segments. (Only V and J exist for light chains)  50 V segments, 25 D segments, and 6 J segments exist and are randomly arranged and rearranged in the genome in a process called [http://en.wikipedia.org/wiki/VDJ_recombination V(D)J recombination]. Each B-cell is programmed to produce antibodies of a single V(D)J recombination order. &lt;br /&gt;
&lt;br /&gt;
Additional diversity is created by the proteins RAG-1 and RAG-2 which introduce the double stranded breaks between V, D, and J segments to allow recombination. At this stage, nucleotides can either be deleted or inserted between adjoining segments before being ligated together. &amp;lt;ref name=&amp;quot;Roit&amp;quot; /&amp;gt; This dramatically increases antibody diversity. Further diversity is created during B-cell proliferation when the variable chains undergo a high rate of point mutations in a process called [http://en.wikipedia.org/wiki/Somatic_hypermutation somatic hypermutation], creating daughter cells of the original B-cell that are slightly different. The antibodies which bind the antigen with the highest affinity are selected for in a process called [http://en.wikipedia.org/wiki/Affinity_maturation affinity maturation]. &amp;lt;ref&amp;gt;PMID:11869898&amp;lt;/ref&amp;gt;&amp;lt;ref&amp;gt;PMID:17337763&amp;lt;/ref&amp;gt; Isotype switching is also possible after activation of the B-cell by a mechanism called “class switch recombination” allowing different immunological responses to the same antigen bound by the same variable regions.&amp;lt;ref&amp;gt;PMID:12884279&amp;lt;/ref&amp;gt; Through this clever system, tens of billions of different glycoprotein antibodies can be created from less than 100 genes, allowing antibodies to bind &amp;lt;scene name=&#039;Antibody/Rituxan_binding_site/1&#039;&amp;gt;structurally complimentary antigens&amp;lt;/scene&amp;gt; with exquisite precision. The discovery of antobdy diversity generation won Susumu Tonegawa the [http://nobelprize.org/nobel_prizes/medicine/laureates/1987/press.html Nobel Prize in Medicine in 1987]. &lt;br /&gt;
&lt;br /&gt;
[[Image:FluorescentCells.jpg|300px|right|thumb| Direct Immuno fluorescence Antibody labeling]]&lt;br /&gt;
{{Clear}}&lt;br /&gt;
==Antibody Applications==&lt;br /&gt;
Detection of particular antibodies is very common in medical diagnostic testing. Numerous biochemical assays exist to detect whether antibodies for specific antigens are present in the blood or other bodily fluids such as antibodies against [http://en.wikipedia.org/wiki/Lyme_disease Lyme disease] or [http://en.wikipedia.org/wiki/HIV HIV], etc. Another common medical test involving antibodies is blood type detection in which an individual’s blood is screened against anti-A and anti-B antibodies to determine the identity of that individual’s [http://en.wikipedia.org/wiki/Blood_type blood antigen type]. &amp;lt;ref&amp;gt;PMID:13477267&amp;lt;/ref&amp;gt; &lt;br /&gt;
&lt;br /&gt;
Antibodies are also extremely powerful tools in the laboratory setting where they are commonly used in [http://en.wikipedia.org/wiki/Western_blot Western Blot] to detect specific proteins in a sample &amp;lt;ref&amp;gt;PMID:6266278&amp;lt;/ref&amp;gt;; [http://en.wikipedia.org/wiki/Flow_cytometry flow cytometry], to differentiate cell types by their protein expression profiles; [http://en.wikipedia.org/wiki/Immunoprecipitation immunoprecipitation], to separate proteins from other compounds in a [http://en.wikipedia.org/wiki/Lysate lysate] and for cellular labeling. Numerous other examples exist. &amp;lt;ref&amp;gt;PMID:15353569&amp;lt;/ref&amp;gt; &lt;br /&gt;
&lt;br /&gt;
The last two decades have seen a dramatic increase in antibody based technologies both for the lab and medicine thanks to the invention of the monoclonal antiboy, a discovery that won Niels K. Jerne, Georges J.F. Köhler, César Milstein the [http://nobelprize.org/nobel_prizes/medicine/laureates/1984/press.html Nobel Prize in Medicine in 1984]. See: [[Monoclonal Antibody]] for additional information. &lt;br /&gt;
&lt;br /&gt;
==3D structures of antibody==&lt;br /&gt;
[[3D structures of antibody]]&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&lt;br /&gt;
==3D Printed Physical Model of an Anitbody==&lt;br /&gt;
&lt;br /&gt;
Shown below is a 3D printed physical model of an Antibody. The protein is displayed as an alpha carbon backbone, with the heavy chains colored white, the light chains colored red, and the glycan colored blue.&lt;br /&gt;
[[Image:antibody1_centerForBioMolecularModeling.jpg|550px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
====The MSOE Center for BioMolecular Modeling====&lt;br /&gt;
&lt;br /&gt;
[[Image:CbmUniversityLogo.jpg | left | 150px]]&lt;br /&gt;
&lt;br /&gt;
The [http://cbm.msoe.edu MSOE Center for BioMolecular Modeling] uses 3D printing technology to create physical models of protein and molecular structures, making the invisible molecular world more tangible and comprehensible. To view more protein structure models, visit our [http://cbm.msoe.edu/educationalmedia/modelgallery/ Model Gallery].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Additional Pages==&lt;br /&gt;
* [[IgA]]&lt;br /&gt;
* [[Epitopes]]&lt;br /&gt;
* [[Major Histocompatibility Complex Class I]]&lt;br /&gt;
* [[Monoclonal Antibody]]&lt;br /&gt;
&lt;br /&gt;
==See Also==&lt;br /&gt;
* [[Variable Lymphocyte Receptors]]&lt;br /&gt;
*Antibody at [[High school teachers&#039; resources]], where you will find tutorials on antibody structure.&lt;br /&gt;
*[http://en.wikipedia.org/wiki/Antibodies Antibodies] at Wikipedia.&lt;br /&gt;
&lt;br /&gt;
[[Category:Topic Page]]&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386117</id>
		<title>Print3D help</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386117"/>
		<updated>2025-10-27T15:17:08Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== Proteopedia and 3D Printing ==&lt;br /&gt;
&lt;br /&gt;
Physical molecular models, by engaging both visual and tactile senses, provide an effective means of deepening the understanding of complex concepts in molecular biology and biochemistry. They allow students to perceive the three-dimensional organization of macromolecules, thereby enhancing comprehension of the relationship between structure and function &amp;lt;ref&amp;gt;PMID: 32590880&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 40214166&amp;lt;/ref&amp;gt;. Numerous studies have demonstrated that the use of tangible models in science education improves learning outcomes, fosters conceptual reasoning, and increases student engagement &amp;lt;ref&amp;gt;PMID: 27366318&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 26712513&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;Larsson, C., Tibell, L.A.E. Challenging Students’ Intuitions—the Influence of a Tangible Model of Virus Assembly on Students’ Conceptual Reasoning About the Process of Self-Assembly. Res Sci Educ 45, 663–690 (2015). [http://dx.doi.org/10.1007/s11165-014-9446-6 DOI: 110.1007/s11165-014-9446-6]&amp;lt;/ref&amp;gt;. The rapid development of 3D-printing technologies has made it possible to create customized and affordable molecular models  &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot;&amp;gt;PMID: 28362403&amp;lt;/ref&amp;gt; &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot;&amp;gt;PMID: 33755300&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 33384761&amp;lt;/ref&amp;gt;. &lt;br /&gt;
&lt;br /&gt;
Affordable desktop 3D printers can now be used to fabricate physical models from virtually any structure or scene on [[Proteopedia]]. This page provides an introduction to 3D printing, a step-by-step guide to generating printable files directly from [[Proteopedia]], and several tested printing profiles for common printers (e.g., Prusa Research, Bambu Lab, Creality, or Elegoo).&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== «3D Printing 101»: an introduction to 3D printing ==&lt;br /&gt;
3D printing, also known as &#039;&#039;additive manufacturing&#039;&#039;, builds physical objects layer by layer from digital designs. For more technical details please head for the excellent introductory article on [https://all3dp.com/2/what-is-3d-printing/ All3DP].  In structural biology education, 3D printing provides an affordable and accessible way to transform atomic coordinate data (e.g., from PDB, MOL or SDF files) into tangible molecular models that can be observed, handled, and discussed in class or laboratory settings.&lt;br /&gt;
&lt;br /&gt;
=== Printer Types: FDM vs. SLA/DLP ===&lt;br /&gt;
The two most accessible 3D-printing technologies that can be used to create molecular models are:&lt;br /&gt;
* &#039;&#039;&#039;FDM (Fused Deposition Modeling)&#039;&#039;&#039;&lt;br /&gt;
This method extrudes a heated thermoplastic filament (such as PLA, PETG or TPU) through a fine nozzle, depositing successive layers that form the model. FDM printers have the advantages of low cost, easy maintenance, wide availability, and being capable of printing large and colorful molecular models. This technology has a few limitations, such as: visible layer lines, lower surface resolution, and less suited for very small or intricate molecular details.&lt;br /&gt;
* &#039;&#039;&#039;SLA/DLP (Resin Printing)&#039;&#039;&#039;&lt;br /&gt;
This technique uses liquid photopolymer resin, cured layer by layer with ultraviolet light. SLA/DLP printers have the advantages of a very high resolution, smooth surfaces and are ideal for compact and detailed models (e.g., small proteins rendered as surface, ligands, or symmetric assemblies). This technology has its own limitations, such as higher material cost, post-processing requirements (washing and UV-curing), and the need for careful handling of resin.&lt;br /&gt;
&lt;br /&gt;
When choosing between FDM and SLA printers, model size and resolution are the key criteria: &#039;&#039;&#039;FDM&#039;&#039;&#039; is preferred for &#039;&#039;large, educational display models&#039;&#039;; &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; is optimal for &#039;&#039;small, precise structures&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
While FDM and SLA/DLP are the most widely used technologies in educational and research contexts due to their accessibility, other additive manufacturing methods also exist —such as &#039;&#039;Selective Laser Sintering&#039;&#039; (SLS), &#039;&#039;PolyJet&#039;&#039;, and &#039;&#039;Binder Jetting&#039;&#039;— each employing different materials and curing mechanisms. These industrial-grade techniques can produce highly detailed or multi-material parts but are generally more expensive and less accessible for classroom use. For an overview of major 3D-printing technologies, see [https://all3dp.com/1/types-of-3d-printers-3d-printing-technology/ All3DP: Complete Overview of the Types of 3D Printers]&lt;br /&gt;
&lt;br /&gt;
=== Single- vs. Multi-Material Printers ===&lt;br /&gt;
Most entry-level desktop 3D printers use a single filament or resin, producing models in one color or material. However, multi-material systems (such as [https://eu.store.bambulab.com/products/ams-multicolor-printing?from=home_web_top_navigation Bambu Lab AMS] and its variants or [https://www.prusa3d.com/category/original-prusa-mmu3/ Prusa MMU3]) can simultaneously print multiple filaments, enabling color-coded domains, subunits, or ligands directly in one print. For complex color information, users can also apply post-print color coding (painting or labeling) or print separate parts and assemble them manually.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A large FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A multi-material FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Small resin-printed models&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:GABAA_receptor.png|320px|center|thumb| GABAA receptor, [[6x3x]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Bacterial_Ribosome_multimaterial_FDM.png|348px|center|thumb| Bacterial 70S ribosome, [[4v5d]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Dna_insuline_sla.png|252px|center|thumb|DNA (left) and insulin (right) models, [[4bna]] and [[4ins]], scale at the bottom in cm]]&lt;br /&gt;
|-&lt;br /&gt;
|Trace Model of the GABAA receptor printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com] &lt;br /&gt;
|Surface model of the Bacterial 70S ribosome printed on a multi-material capable printer (BambuLab X1C AMS). Blue and violet are ribosomal proteins, orange and yellow are rRNAs, and black is tRNA. Printable files available on [https://www.printables.com/model/1430877-bacterial-70s-ribosome Printables.com]&lt;br /&gt;
|Balls and sticks and cartoon models of DNA (right) and insulin (left)&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== File Formats Used in 3D Printing ===&lt;br /&gt;
Proteopedia supports two export formats for generating printable molecular models:&lt;br /&gt;
*&#039;&#039;&#039;.STL&#039;&#039;&#039; (Stereolithography): the most common and universally compatible format; encodes only surface geometry, without color or texture information.&lt;br /&gt;
*&#039;&#039;&#039;.OBJ&#039;&#039;&#039; (Wavefront Object) with an associated &#039;&#039;&#039;.MTL&#039;&#039;&#039; (Material Template Library) files: includes both geometry and optional color/texture data; useful for color prints.&lt;br /&gt;
&lt;br /&gt;
Another widely adopted file format used in 3D printing is the &#039;&#039;&#039;.3MF&#039;&#039;&#039; (3D Manufacturing Format): a modern open standard that stores geometry, color, and multi-material metadata in a single file—recommended for advanced printers. For a more extensive pros and cons of different 3D printing file formats please see [https://all3dp.com/2/3d-file-format-3d-model-types/ The Main 3D Printing File Formats on all3dp]. &lt;br /&gt;
&lt;br /&gt;
STL is ideal for single-color models and maximum compatibility, while OBJ/MTL is recommended for multi-material workflows. 3MF files will be used in this tutorial to save the model and printing settings. &lt;br /&gt;
&lt;br /&gt;
Support in Proteopedia for these formats is based on the export capabilities of Jmol/JSmol; for details, see [http://wiki.jmol.org/index.php/File_formats/3D_Objects#STL STL] and [http://wiki.jmol.org/index.php/File_formats/3D_Objects#OBJ OBJ]&lt;br /&gt;
&lt;br /&gt;
== Overview of the 3D printing process ==&lt;br /&gt;
3D printing enables the transformation of atomic-level structural data into tangible macromolecular models that can be explored through both sight and touch.  &lt;br /&gt;
The process generally follows several main steps, each requiring specific types of software and hardware.&lt;br /&gt;
[[Image:3D_printing_workflow_v2.png|thumb|left|400px|Overview of the 3D printing workflow for generating physical molecular models.]]&lt;br /&gt;
	&lt;br /&gt;
=== Preparing the structure and generating a printable File ===&lt;br /&gt;
:The first stage involves creating a printable three-dimensional representation of the molecule. Some molecular-graphics programs such as [https://www.pymol.org/ PyMOL], [https://www.rbvi.ucsf.edu/chimerax/ UCSF ChimeraX], [https://molstar.org/Mol*], or [https://jmol.sourceforge.net/ Jmol] can be used not only to visualize a structure (from the Protein Data Bank or other sources), but also to export the resulting geometry in a .STL or .OBJ format. However, the default visualization styles of these programs are &#039;&#039;&#039;&#039;&#039;not directly suitable for 3D printing&#039;&#039;&#039;&#039;&#039;. Therefore, when preparing a model for fabrication, it is important to:&lt;br /&gt;
:* &#039;&#039;&#039;Select an appropriate molecular representation&#039;&#039;&#039; (e.g., surface, cartoon, sticks, spheres) depending on the pedagogical or structural feature you wish to highlight.  &lt;br /&gt;
:* &#039;&#039;&#039;Add struts or connectors&#039;&#039;&#039; to increase the mechanical stability of the model, especially for large complexes or long helices.  &lt;br /&gt;
:* &#039;&#039;&#039;Remove specific struts or pseudobonds&#039;&#039;&#039; when individual components — ligands, subunits, or cofactors — need to remain detachable.  &lt;br /&gt;
:* &#039;&#039;&#039;Adjust thickness&#039;&#039;&#039; of atoms, bonds, helices, and sheets to ensure adequate rigidity and printability (features thinner than the printer’s nozzle diameter or resin resolution may break).  &lt;br /&gt;
:* &#039;&#039;&#039;Apply meaningful coloring&#039;&#039;&#039; when preparing multi-material prints, for instance, to distinguish domains, chains, ligands or atoms.&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene that automates the process and enables users to effortlessly generate 3D-printable molecular models - more on that in the corresponding section [[#Generating printable files on Proteopedia|Generating printable files on Proteopedia]] within this page. For advanced users wanting to do this manually, we highly recommend two guides: &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot; /&amp;gt; and &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
=== Slicing the Model ===&lt;br /&gt;
Before printing, the STL file must be processed by a &#039;&#039;&#039;slicer&#039;&#039;&#039; — specialized software that converts 3D geometry into a series of horizontal layers. The slicer also generates &#039;&#039;&#039;G-code&#039;&#039;&#039;, the set of instructions that control the printer. These commands are printer-specific and include parameters such as extrusion speed, layer thickness, temperature, and movement. Together, they are usually stored as a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;.  &lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an FDM printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;number of perimeters&#039;&#039;&#039;, which affects mechanical strength and print time;&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines resolution and print duration;&lt;br /&gt;
:* &#039;&#039;&#039;infill density&#039;&#039;&#039;, which determines internal strength and affects print time;&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, temporary structures that hold overhanging regions;&lt;br /&gt;
:* &#039;&#039;&#039;print orientation&#039;&#039;&#039;, which influences surface quality, mechanical strength, and the amount of supports required.&lt;br /&gt;
:All these parameters make up a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. In this step, users must also select the material-specific parameters, or apply a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. More details on these profiles are provided later on this page.&lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines vertical resolution and print time; thinner layers produce smoother surfaces but significantly increase printing duration.&lt;br /&gt;
:* &#039;&#039;&#039;exposure time&#039;&#039;&#039;, which controls how long each layer is cured by UV light; optimal exposure ensures proper adhesion between layers without over-curing fine details.&lt;br /&gt;
:* &#039;&#039;&#039;bottom-layer exposure and count&#039;&#039;&#039;, which influence model adhesion to the build platform — longer exposures and additional base layers improve stability during printing.&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, which anchor the model to the build plate and prevent deformation during peeling; proper placement reduces surface marks and print failures.&lt;br /&gt;
:* &#039;&#039;&#039;model orientation&#039;&#039;&#039;, which affects surface quality, support contact area, and resin drainage; angling the model (typically 30–45°) minimizes suction forces and improves print reliability.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for FDM printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for resin printing&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:Insuline_sliced_prusa.gif|386px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|[[Image:Insuline_Sliced_SLA.gif|372px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|-&lt;br /&gt;
|Cartoon model of insulin sliced in PrusaSlicer and ready to be printed on FDM printers. The arrow shows the trajectory of the print head on a single slice or layer. Orange is the model, green are the supports. &lt;br /&gt;
|Cartoon model of insulin sliced in Elegoo SatelLite and ready to be printed on FDM printer.On the left, with blue is the model, with gray are the supports. On the right is the image on the UV screen. &lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== 3D Printing the Model ===&lt;br /&gt;
:The prepared G-code is then transferred to the 3D printer, either via an SD card, USB flash drive, or Wi-Fi connection. During printing, close observation of the first few layers is essential to ensure good adhesion to the build plate and a successful print. Total printing time depends on model size, selected layer height, and printer speed. &#039;&#039;Small peptide&#039;&#039; models may print in &#039;&#039;&#039;less than an hour&#039;&#039;&#039;, whereas l&#039;&#039;arge multimeric assemblies&#039;&#039; can require &#039;&#039;&#039;several hours or days&#039;&#039;&#039;. &#039;&#039;Multi-color&#039;&#039; or &#039;&#039;multi-material&#039;&#039; prints generally take &#039;&#039;&#039;longer&#039;&#039;&#039;, while &#039;&#039;SLA/DLP&#039;&#039; printers are generally &#039;&#039;&#039;faster&#039;&#039;&#039; due to their simultaneous layer exposure.&lt;br /&gt;
=== Post-Processing ===&lt;br /&gt;
:After printing, the model undergoes post-processing, which varies depending on the printing technology used:&lt;br /&gt;
:* For &#039;&#039;&#039;FDM prints&#039;&#039;&#039;, supports are removed mechanically, and surfaces can be smoothed by light sanding or polishing.&lt;br /&gt;
:* For &#039;&#039;&#039;resin prints&#039;&#039;&#039;, supports are removed mechanically, parts are washed in isopropanol to remove uncured resin and then exposed to UV light for final curing.&lt;br /&gt;
:Models printed in multiple parts can be assembled using cyanoacrylate or epoxy adhesive. Optional finishing steps (painting, labeling) can improve contrast between subunits or highlight functional regions.&lt;br /&gt;
&lt;br /&gt;
==Generating printable files on Proteopedia==&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene, enabling logged-in users to effortlessly generate 3D-printable molecular models directly from its pages. The tool is powered by [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;], a script that analyzes the structural data and automatically scales the model’s geometry to match the printable volume of a medium-size desktop 3D printer (e.g., Ender-3, 210×210×210 mm). During this process, the tool evaluates the molecular bounding box, atom radii, and bond lengths, then proportionally adjusts all dimensions to achieve a realistic and mechanically robust print scale — preserving scientific accuracy while ensuring manufacturability. For advanced users, [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;] may also be used in conjunction with the [https://jmol.sourceforge.net/ &#039;&#039;&#039;Jmol&#039;&#039;&#039;] program, providing full access to its scripting capabilities and advanced export features.&lt;br /&gt;
==Step-by-step guide for automatic generation of printable files on Proteopedia==&lt;br /&gt;
=== Open a structure and access the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool ===&lt;br /&gt;
Log in with your Proteopedia Username and password. Navigate to any Proteopedia page (for example, [[Introduction_to_protein_structure]]). The corresponding 3D structure will load in the viewer on the right.  &lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_button_in_Proteopedia.png|thumb|left|400px|The &#039;&#039;&#039;Print3D&#039;&#039;&#039; button on a Proteopedia page]]&lt;br /&gt;
&lt;br /&gt;
At the bottom of the structure display window, locate and click the &#039;&#039;&#039;Print3D&#039;&#039;&#039; button. The tool will launch and begin analyzing the current molecular structure.  &lt;br /&gt;
This process may take some time to complete, depending on the size of the structure.  &lt;br /&gt;
Please wait until the message &#039;&#039;&#039;Analyzing structure...&#039;&#039;&#039; disappears and the next page is displayed — this marks the start of the two-step printing workflow.&lt;br /&gt;
=== Select a molecular representation and a printing scale ===&lt;br /&gt;
In this new page, some user input is required. Each option includes a short explanation; the key steps are outlined below, but feel free to explore and adopt the settings that best fit your use case.&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step1.png|thumb|left|400px|Selecting molecular representation and printing scale]]&lt;br /&gt;
&lt;br /&gt;
(1) &#039;&#039;&#039;Choose a molecular representation&#039;&#039;&#039; from the &#039;&#039;&#039;Scheme&#039;&#039;&#039; list, based on your goal:&lt;br /&gt;
* &#039;&#039;&#039;Backbone&#039;&#039;&#039;, &#039;&#039;&#039;Trace&#039;&#039;&#039;, or &#039;&#039;&#039;Ribbon&#039;&#039;&#039; — to emphasize secondary structure (effective for teaching protein folds).&lt;br /&gt;
* &#039;&#039;&#039;Surface&#039;&#039;&#039; — to highlight molecular topology and binding sites.&lt;br /&gt;
* &#039;&#039;&#039;Ball &amp;amp; Stick&#039;&#039;&#039; — atom-level detail for ligands or small molecules; usually impractical for large proteins or complexes.&lt;br /&gt;
* &#039;&#039;&#039;Proteopedia Scene&#039;&#039;&#039; — attempts to render the current page’s scene directly; may not work for all scenes. This is not fully implemented and only available for a few users.&lt;br /&gt;
&#039;&#039;Note:&#039;&#039; Some representations may be unavailable for a given structure because they are not printable in a reliable way.&lt;br /&gt;
&lt;br /&gt;
(2) In the &#039;&#039;&#039;Printer&#039;&#039;&#039; section, select whether you want a &#039;&#039;&#039;single-color&#039;&#039;&#039; or a &#039;&#039;&#039;multi-color&#039;&#039;&#039; print.&lt;br /&gt;
&lt;br /&gt;
(3) In the &#039;&#039;&#039;Printer scale&#039;&#039;&#039; section, set the desired size of the printed model. The tool constrains safe sizes based on the chosen representation and displays the physical dimensions (mm). &#039;&#039;&#039;Important! Please note the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;printer scale value in %&amp;lt;/span&amp;gt; as it is going to be required downstream in the next section of this workflow, [[#Printing files from Proteopedia|Printing files from Proteopedia]]&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
(4) When ready, click the green &#039;&#039;&#039;Make printer files&#039;&#039;&#039; button. Please wait patiently until the  &#039;&#039;Generating files for 3D printing of...&#039;&#039; message disappears and the final step is displayed.&lt;br /&gt;
&lt;br /&gt;
===Download the .STL or .OBJ files===&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step2.png|thumb|left|400px|Final step in generating printable files]]&lt;br /&gt;
&lt;br /&gt;
In this final page, a 3D preview of the generated model is displayed.&lt;br /&gt;
You can use the mouse to rotate, zoom, and inspect the model from different angles. If the result meets your needs, click the green (A) &#039;&#039;&#039;Download files&#039;&#039;&#039; button and save the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive containing the &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; files on your computer. If your model needs further improvements, hit the green (B) &#039;&#039;&#039;Same structure&#039;&#039;&#039; button to return to the previous screen and adjust your settings.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
{{clear}}&lt;br /&gt;
== Printing files from Proteopedia ==&lt;br /&gt;
Unzipping the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive will produce the exported &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file, along with an optional &#039;&#039;&#039;.MTL&#039;&#039;&#039; material file. &lt;br /&gt;
=== Using 3D printing services ===&lt;br /&gt;
If you do not have a 3D printer, you can still obtain physical models by using locally available 3D-printing services. Just search on [https://www.google.com/maps Google Maps] with the term  &#039;&#039;&#039;3D printing&#039;&#039;&#039; in your area. Here is short list of well-known 3D Printing service providers that may also ship worldwide: &lt;br /&gt;
&lt;br /&gt;
* [https://www.shapeways.com/ &#039;&#039;&#039;Shapeways&#039;&#039;&#039;] — global service offering a wide range of materials and colors. Educational discounts are available through their academic program.&lt;br /&gt;
* [https://www.sculpteo.com/en/ &#039;&#039;&#039;Sculpteo&#039;&#039;&#039;] — Europe-based provider offering fast turnaround and many printing technologies, including resin and polymer options.&lt;br /&gt;
* [https://www.xometry.com/capabilities/3d-printing-service &#039;&#039;&#039;Xometry&#039;&#039;&#039;] — large international network providing access to industrial-grade printing methods such as FDM, SLA, SLS, and DMLS.&lt;br /&gt;
* [https://craftcloud3d.com/ &#039;&#039;&#039;Craftcloud&#039;&#039;&#039;] — an aggregator that compares multiple providers and finds the best price and lead time for your uploaded model.&lt;br /&gt;
&lt;br /&gt;
When contacting a printing service, provide the exported files together with the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value in %&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ([[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). It is also advisable to share the link to this Proteopedia page so that the operator understands the peculiarities of printing molecular models. &lt;br /&gt;
&lt;br /&gt;
=== Using a desktop 3D printer ===&lt;br /&gt;
&lt;br /&gt;
Before importing the .STL or .OBJ file into your slicer software, it is recommended to inspect and, if necessary, repair the model to ensure printability. Common issues include non-manifold geometry, intersecting faces, and missing surfaces.  The example below demonstrates how to use [https://www.blender.org/ &#039;&#039;&#039;Blender&#039;&#039;&#039;] together with its [https://extensions.blender.org/add-ons/print3d-toolbox/ &#039;&#039;&#039;3D Print Toolbox extension&#039;&#039;&#039;] to improve the printability of the .STL and .OBJ files generated with the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in [[Proteopedia]]. &#039;&#039;&#039;Important note&#039;&#039;&#039;: The repair process is largely automated but may introduce artifacts. Carefully inspect the corrected model for any missing or distorted sections, atoms, or bonds, and determine whether these omissions affect the intended purpose of the printed model.  &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for single color or resin printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for multi-color FDM printing&lt;br /&gt;
|-&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=k6u-5JnoP-c&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=OCisrIZMIDM&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|}  &lt;br /&gt;
&lt;br /&gt;
Once the repaired &#039;&#039;&#039;.STL or .OBJ&#039;&#039;&#039; file is ready, it can be imported into your slicer software. In this step, you will prepare the file for printing by applying appropriate printer, filament, and print-settings profiles.&lt;br /&gt;
&lt;br /&gt;
*Apply the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value (%)&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ( [[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). This step ensures that the model fits your print bed and maintains structural integrity during printing. The location of the scale (%) input field varies depending on the slicer software you are using.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Orient the model on the print bed&#039;&#039;&#039; so that its largest, flattest surface rests on the bed. This minimizes the need for supports and improves adhesion. If your slicer includes an Auto Orient or Auto Arrange function, use it to optimize placement. (&#039;&#039;Hint&#039;&#039;: Bambu Studio and Orca Slicer include this feature, Ultimaker Cura has a [https://marketplace.ultimaker.com/app/cura/plugins/nallath/OrientationPlugin Auto-Orientation plugin] available, while PrusaSlicer currently does not.)&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Select the printer&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that matches your device.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Choose the material&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; corresponding to the filament type (e.g., PLA, PETG, TPU) and manufacturer you intend to use.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Adjust the printing parameters&#039;&#039;&#039; by selecting a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that defines layer height, infill, speed, and support options.&lt;br /&gt;
&lt;br /&gt;
In most cases, the default &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; and &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; provided by the slicer are sufficient. However, molecular models often include overhangs, thin connections, and complex internal geometries, which require additional supports and reinforced perimeters to ensure structural stability. For this reason, the default &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; may not yield optimal results.&lt;br /&gt;
&lt;br /&gt;
Validated printing profiles for the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool are available for several printer models. These profiles provide optimized settings that produce sturdy models, reduce material consumption, and shorten print time, ensuring consistent and reliable results. Three distinct profiles are supplied, corresponding to major molecular representations: &#039;&#039;&#039;balls and sticks&#039;&#039;&#039;, &#039;&#039;&#039;surface&#039;&#039;&#039;, and &#039;&#039;&#039;cartoon&#039;&#039;&#039;. The &#039;&#039;&#039;cartoon&#039;&#039;&#039; profile is also suitable for &#039;&#039;&#039;backbone&#039;&#039;&#039;, &#039;&#039;&#039;trace&#039;&#039;&#039;, and &#039;&#039;&#039;ribbon&#039;&#039;&#039; representations. For some printers, each profile is supplied in two variants, one using standard supports and one using tree or organic supports. In the case of multi-material printers, profiles for printing with soluble support and soluble interface are also provided.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer brand and model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Profiles provided as / Slicer&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer Type, nozle size and multi-material support&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |GitHub with profiles&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to import profiles into Slicer&lt;br /&gt;
|-&lt;br /&gt;
|Original Prusa Core One&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer ]&lt;br /&gt;
|FDM / 0.4 mm / yes, 5 colors, if MMU3 installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/Prusa%20CoreOne CoreOne]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab A1Mini&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, 4 colors if AMS Lite is installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/BambuLab%20A1Mini AiMini]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab X1 Carbon&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, up to 16 colors if multiple AMS are installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ca92e7de9c72505c1b9b09e912ad177341cabc9a/BambuLab%20X1C X1Carbon]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|- &lt;br /&gt;
|Original Prusa MK3S+&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/7a7ee68d1e19f063600f53def49a99dfefbc595d/Prusa%20MK3S%2B MK3S+]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 5 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/a653c7cc6b3dec86b90117cc450d1883cc4a80bd/Ender-5-Pro Ender5Pro]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 3 v2 with a ENDERIDEX kit&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / yes, IDEX, two filaments&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/c2c74f1261a42c160e7e3898a407f21465de2ca7/Ender3-IDEX Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Kingroon KPS3 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ea733b2d05020b99f91c92f71a039c5ba8e54108/Kingroon-KPS3-Pro Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Elegoo Mars 5 Ultra&lt;br /&gt;
|no profile needed, just be sure to add supports / [https://www.elegoo.com/pages/satellite-3d-slicer?srsltid=AfmBOopMQGHgHycHMFOZALzOIC8z7bVlSHjL_jj2ShYR4QkowYKmKzUx ELEGOO SatelLite]&lt;br /&gt;
|resin / - / no&lt;br /&gt;
|&lt;br /&gt;
|no profile needed, default settings worked, just be sure to add supports. EVO supports worked well enough.  Post-processing steps: 1)washing: at least 10 min. 2) support removal 3)curring: at least 10 min on a Elegoo Mercury Plus V3.0&lt;br /&gt;
|- &lt;br /&gt;
|} &lt;br /&gt;
&#039;&#039;&#039;Notes&#039;&#039;&#039;: &lt;br /&gt;
* These profiles were developed and validated with the support of EDUMOL3D, Project [http://cercetare.bio.uaic.ro/grupuri/bioactive/content/grants/PED2024_mm.html PN-IV-P7-7.1-PED-2024-0343] financed by the Ministry of Research, Innovation and Digitization, [https://uefiscdi.gov.ro/ UEFISCDI], Romania.&lt;br /&gt;
* The profiles are a work in progress. Please check GitHub for updates. If you have suggestions for improvements, please drop a message at marius.mihasan(@)uaic.ro&lt;br /&gt;
&lt;br /&gt;
==== &#039;&#039;&#039;Note on multi-color printing &#039;&#039;&#039; ====&lt;br /&gt;
To our knowledge, only &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039; and &#039;&#039;&#039;Orca Slicer&#039;&#039;&#039; can automatically import color information from the &#039;&#039;&#039;.MTL&#039;&#039;&#039; file associated with the printable &#039;&#039;&#039;.OBJ&#039;&#039;&#039; generated by the Proteopedia &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool.  &lt;br /&gt;
At present, &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; does not support importing &#039;&#039;&#039;.MTL&#039;&#039;&#039; files directly.&lt;br /&gt;
&lt;br /&gt;
A practical workaround for &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; users is as follows:  &lt;br /&gt;
# Open the &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file in &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039;.  &lt;br /&gt;
#Verify or adjust the color mapping as needed.  &lt;br /&gt;
#Export the model as a generic &#039;&#039;&#039;.3MF&#039;&#039;&#039; file using the menu command:  &#039;&#039;File&#039;&#039; → &#039;&#039;Export&#039;&#039; → &#039;&#039;Export Generic 3MF...&#039;&#039;  &lt;br /&gt;
#Open the exported &#039;&#039;&#039;.3MF&#039;&#039;&#039; file in &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;. The color data will now be available under the &#039;&#039;&#039;Multimaterial Painting&#039;&#039;&#039; tool.&lt;br /&gt;
&lt;br /&gt;
This workflow preserves the original coloring assigned in Proteopedia and allows successful multi-color or multi-material printing on any capable 3D printer compatible with &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Other relevant resources ==&lt;br /&gt;
[[User:Marius_Mihasan/Print3D_models_gallery]] - examples of 3D printed molecular models from Proteopedia users.&lt;br /&gt;
&lt;br /&gt;
[https://3d.nih.gov/ NIH 3D Print Exchange] - an open, community-driven portal to download, share, and create bioscientific and medical 3D models, including for 3D printing.&lt;br /&gt;
  &lt;br /&gt;
[https://github.com/mariusmihasan/3DP-Jmol 3DP-Jmol] - the Jmol/JSmol behind the Print3D tool. Automatically generates 3D printable molecular models from structural data and can be easily integrated into web pages.&lt;br /&gt;
&lt;br /&gt;
[https://pdb101.rcsb.org/learn/3d-printing/pdb-structures-and-3d-printing 3D Printing on PDB101] - a quick guide on 3D printing molecular models and a small curated 3D models for education&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;If you print a model from Proteopedia, please share photos and feedback — let’s 3D print the whole Proteopedia!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386108</id>
		<title>Print3D help</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386108"/>
		<updated>2025-10-27T10:14:24Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== Proteopedia and 3D Printing ==&lt;br /&gt;
&lt;br /&gt;
Physical molecular models, by engaging both visual and tactile senses, provide an effective means of deepening the understanding of complex concepts in molecular biology and biochemistry. They allow students to perceive the three-dimensional organization of macromolecules, thereby enhancing comprehension of the relationship between structure and function &amp;lt;ref&amp;gt;PMID: 32590880&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 40214166&amp;lt;/ref&amp;gt;. Numerous studies have demonstrated that the use of tangible models in science education improves learning outcomes, fosters conceptual reasoning, and increases student engagement &amp;lt;ref&amp;gt;PMID: 27366318&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 26712513&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;Larsson, C., Tibell, L.A.E. Challenging Students’ Intuitions—the Influence of a Tangible Model of Virus Assembly on Students’ Conceptual Reasoning About the Process of Self-Assembly. Res Sci Educ 45, 663–690 (2015). [http://dx.doi.org/10.1007/s11165-014-9446-6 DOI: 110.1007/s11165-014-9446-6]&amp;lt;/ref&amp;gt;. The rapid development of 3D-printing technologies has made it possible to create customized and affordable molecular models  &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot;&amp;gt;PMID: 28362403&amp;lt;/ref&amp;gt; &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot;&amp;gt;PMID: 33755300&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 33384761&amp;lt;/ref&amp;gt;. &lt;br /&gt;
&lt;br /&gt;
Affordable desktop 3D printers can now be used to fabricate physical models from virtually any structure or scene on [[Proteopedia]]. This page provides an introduction to 3D printing, a step-by-step guide to generating printable files directly from [[Proteopedia]], and several tested printing profiles for common printers (e.g., Prusa Research, Bambu Lab, Creality, or Elegoo).&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== «3D Printing 101»: an introduction to 3D printing ==&lt;br /&gt;
3D printing, also known as &#039;&#039;additive manufacturing&#039;&#039;, builds physical objects layer by layer from digital designs. For more technical details please head for the excellent introductory article on [https://all3dp.com/2/what-is-3d-printing/ All3DP].  In structural biology education, 3D printing provides an affordable and accessible way to transform atomic coordinate data (e.g., from PDB, MOL or SDF files) into tangible molecular models that can be observed, handled, and discussed in class or laboratory settings.&lt;br /&gt;
&lt;br /&gt;
=== Printer Types: FDM vs. SLA/DLP ===&lt;br /&gt;
The two most accessible 3D-printing technologies that can be used to create molecular models are:&lt;br /&gt;
* &#039;&#039;&#039;FDM (Fused Deposition Modeling)&#039;&#039;&#039;&lt;br /&gt;
This method extrudes a heated thermoplastic filament (such as PLA, PETG or TPU) through a fine nozzle, depositing successive layers that form the model. FDM printers have the advantages of low cost, easy maintenance, wide availability, and being capable of printing large and colorful molecular models. This technology has a few limitations, such as: visible layer lines, lower surface resolution, and less suited for very small or intricate molecular details.&lt;br /&gt;
* &#039;&#039;&#039;SLA/DLP (Resin Printing)&#039;&#039;&#039;&lt;br /&gt;
This technique uses liquid photopolymer resin, cured layer by layer with ultraviolet light. SLA/DLP printers have the advantages of a very high resolution, smooth surfaces and are ideal for compact and detailed models (e.g., small proteins rendered as surface, ligands, or symmetric assemblies). This technology has its own limitations, such as higher material cost, post-processing requirements (washing and UV-curing), and the need for careful handling of resin.&lt;br /&gt;
&lt;br /&gt;
When choosing between FDM and SLA printers, model size and resolution are the key criteria: &#039;&#039;&#039;FDM&#039;&#039;&#039; is preferred for &#039;&#039;large, educational display models&#039;&#039;; &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; is optimal for &#039;&#039;small, precise structures&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
While FDM and SLA/DLP are the most widely used technologies in educational and research contexts due to their accessibility, other additive manufacturing methods also exist —such as &#039;&#039;Selective Laser Sintering&#039;&#039; (SLS), &#039;&#039;PolyJet&#039;&#039;, and &#039;&#039;Binder Jetting&#039;&#039;— each employing different materials and curing mechanisms. These industrial-grade techniques can produce highly detailed or multi-material parts but are generally more expensive and less accessible for classroom use. For an overview of major 3D-printing technologies, see [https://all3dp.com/1/types-of-3d-printers-3d-printing-technology/ All3DP: Complete Overview of the Types of 3D Printers]&lt;br /&gt;
&lt;br /&gt;
=== Single- vs. Multi-Material Printers ===&lt;br /&gt;
Most entry-level desktop 3D printers use a single filament or resin, producing models in one color or material. However, multi-material systems (such as [https://eu.store.bambulab.com/products/ams-multicolor-printing?from=home_web_top_navigation Bambu Lab AMS] and its variants or [https://www.prusa3d.com/category/original-prusa-mmu3/ Prusa MMU3]) can simultaneously print multiple filaments, enabling color-coded domains, subunits, or ligands directly in one print. For complex color information, users can also apply post-print color coding (painting or labeling) or print separate parts and assemble them manually.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A large FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A multi-material FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Small resin-printed models&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:GABAA_receptor.png|320px|center|thumb| GABAA receptor, [[6x3x]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Bacterial_Ribosome_multimaterial_FDM.png|348px|center|thumb| Bacterial 70S ribosome, [[4v5d]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Dna_insuline_sla.png|252px|center|thumb|DNA (left) and insulin (right) models, [[4bna]] and [[4ins]], scale at the bottom in cm]]&lt;br /&gt;
|-&lt;br /&gt;
|Trace Model of the GABAA receptor printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com] &lt;br /&gt;
|Surface model of the Bacterial 70S ribosome printed on a multi-material capable printer (BambuLab X1C AMS). Blue and violet are ribosomal proteins, orange and yellow are rRNAs, and black is tRNA. Printable files available on [https://www.printables.com/model/1430877-bacterial-70s-ribosome Printables.com]&lt;br /&gt;
|Balls and sticks and cartoon models of DNA (right) and insulin (left)&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== File Formats Used in 3D Printing ===&lt;br /&gt;
Proteopedia supports two export formats for generating printable molecular models:&lt;br /&gt;
*&#039;&#039;&#039;.STL&#039;&#039;&#039; (Stereolithography): the most common and universally compatible format; encodes only surface geometry, without color or texture information.&lt;br /&gt;
*&#039;&#039;&#039;.OBJ&#039;&#039;&#039; (Wavefront Object) with an associated &#039;&#039;&#039;.MTL&#039;&#039;&#039; (Material Template Library) files: includes both geometry and optional color/texture data; useful for color prints.&lt;br /&gt;
&lt;br /&gt;
Another widely adopted file format used in 3D printing is the &#039;&#039;&#039;.3MF&#039;&#039;&#039; (3D Manufacturing Format): a modern open standard that stores geometry, color, and multi-material metadata in a single file—recommended for advanced printers. For a more extensive pros and cons of different 3D printing file formats please see [https://all3dp.com/2/3d-file-format-3d-model-types/ The Main 3D Printing File Formats on all3dp]. &lt;br /&gt;
&lt;br /&gt;
STL is ideal for single-color models and maximum compatibility, while OBJ/MTL is recommended for multi-material workflows. 3MF files will be used in this tutorial to save the model and printing settings. &lt;br /&gt;
&lt;br /&gt;
Support in Proteopedia for these formats is based on the export capabilities of Jmol/JSmol; for details, see [http://wiki.jmol.org/index.php/File_formats/3D_Objects#STL STL] and [http://wiki.jmol.org/index.php/File_formats/3D_Objects#OBJ OBJ]&lt;br /&gt;
&lt;br /&gt;
== Overview of the 3D printing process ==&lt;br /&gt;
3D printing enables the transformation of atomic-level structural data into tangible macromolecular models that can be explored through both sight and touch.  &lt;br /&gt;
The process generally follows several main steps, each requiring specific types of software and hardware.&lt;br /&gt;
[[Image:3D_printing_workflow_v2.png|thumb|left|400px|Overview of the 3D printing workflow for generating physical molecular models.]]&lt;br /&gt;
	&lt;br /&gt;
=== Preparing the structure and generating a printable File ===&lt;br /&gt;
:The first stage involves creating a printable three-dimensional representation of the molecule. Some molecular-graphics programs such as [https://www.pymol.org/ PyMOL], [https://www.rbvi.ucsf.edu/chimerax/ UCSF ChimeraX], [https://molstar.org/Mol*], or [https://jmol.sourceforge.net/ Jmol] can be used not only to visualize a structure (from the Protein Data Bank or other sources), but also to export the resulting geometry in a .STL or .OBJ format. However, the default visualization styles of these programs are &#039;&#039;&#039;&#039;&#039;not directly suitable for 3D printing&#039;&#039;&#039;&#039;&#039;. Therefore, when preparing a model for fabrication, it is important to:&lt;br /&gt;
:* &#039;&#039;&#039;Select an appropriate molecular representation&#039;&#039;&#039; (e.g., surface, cartoon, sticks, spheres) depending on the pedagogical or structural feature you wish to highlight.  &lt;br /&gt;
:* &#039;&#039;&#039;Add struts or connectors&#039;&#039;&#039; to increase the mechanical stability of the model, especially for large complexes or long helices.  &lt;br /&gt;
:* &#039;&#039;&#039;Remove specific struts or pseudobonds&#039;&#039;&#039; when individual components — ligands, subunits, or cofactors — need to remain detachable.  &lt;br /&gt;
:* &#039;&#039;&#039;Adjust thickness&#039;&#039;&#039; of atoms, bonds, helices, and sheets to ensure adequate rigidity and printability (features thinner than the printer’s nozzle diameter or resin resolution may break).  &lt;br /&gt;
:* &#039;&#039;&#039;Apply meaningful coloring&#039;&#039;&#039; when preparing multi-material prints, for instance, to distinguish domains, chains, ligands or atoms.&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene that automates the process and enables users to effortlessly generate 3D-printable molecular models - more on that in the corresponding section [[#Generating printable files on Proteopedia|Generating printable files on Proteopedia]] within this page. For advanced users wanting to do this manually, we highly recommend two guides: &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot; /&amp;gt; and &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
=== Slicing the Model ===&lt;br /&gt;
Before printing, the STL file must be processed by a &#039;&#039;&#039;slicer&#039;&#039;&#039; — specialized software that converts 3D geometry into a series of horizontal layers. The slicer also generates &#039;&#039;&#039;G-code&#039;&#039;&#039;, the set of instructions that control the printer. These commands are printer-specific and include parameters such as extrusion speed, layer thickness, temperature, and movement. Together, they are usually stored as a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;.  &lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an FDM printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;number of perimeters&#039;&#039;&#039;, which affects mechanical strength and print time;&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines resolution and print duration;&lt;br /&gt;
:* &#039;&#039;&#039;infill density&#039;&#039;&#039;, which determines internal strength and affects print time;&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, temporary structures that hold overhanging regions;&lt;br /&gt;
:* &#039;&#039;&#039;print orientation&#039;&#039;&#039;, which influences surface quality, mechanical strength, and the amount of supports required.&lt;br /&gt;
:All these parameters make up a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. In this step, users must also select the material-specific parameters, or apply a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. More details on these profiles are provided later on this page.&lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines vertical resolution and print time; thinner layers produce smoother surfaces but significantly increase printing duration.&lt;br /&gt;
:* &#039;&#039;&#039;exposure time&#039;&#039;&#039;, which controls how long each layer is cured by UV light; optimal exposure ensures proper adhesion between layers without over-curing fine details.&lt;br /&gt;
:* &#039;&#039;&#039;bottom-layer exposure and count&#039;&#039;&#039;, which influence model adhesion to the build platform — longer exposures and additional base layers improve stability during printing.&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, which anchor the model to the build plate and prevent deformation during peeling; proper placement reduces surface marks and print failures.&lt;br /&gt;
:* &#039;&#039;&#039;model orientation&#039;&#039;&#039;, which affects surface quality, support contact area, and resin drainage; angling the model (typically 30–45°) minimizes suction forces and improves print reliability.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for FDM printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for resin printing&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:Insuline_sliced_prusa.gif|386px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|[[Image:Insuline_Sliced_SLA.gif|372px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|-&lt;br /&gt;
|Cartoon model of insulin sliced in PrusaSlicer and ready to be printed on FDM printers. The arrow shows the trajectory of the print head on a single slice or layer. Orange is the model, green are the supports. &lt;br /&gt;
|Cartoon model of insulin sliced in Elegoo SatelLite and ready to be printed on FDM printer.On the left, with blue is the model, with gray are the supports. On the right is the image on the UV screen. &lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== 3D Printing the Model ===&lt;br /&gt;
:The prepared G-code is then transferred to the 3D printer, either via an SD card, USB flash drive, or Wi-Fi connection. During printing, close observation of the first few layers is essential to ensure good adhesion to the build plate and a successful print. Total printing time depends on model size, selected layer height, and printer speed. &#039;&#039;Small peptide&#039;&#039; models may print in &#039;&#039;&#039;less than an hour&#039;&#039;&#039;, whereas l&#039;&#039;arge multimeric assemblies&#039;&#039; can require &#039;&#039;&#039;several hours or days&#039;&#039;&#039;. &#039;&#039;Multi-color&#039;&#039; or &#039;&#039;multi-material&#039;&#039; prints generally take &#039;&#039;&#039;longer&#039;&#039;&#039;, while &#039;&#039;SLA/DLP&#039;&#039; printers are generally &#039;&#039;&#039;faster&#039;&#039;&#039; due to their simultaneous layer exposure.&lt;br /&gt;
=== Post-Processing ===&lt;br /&gt;
:After printing, the model undergoes post-processing, which varies depending on the printing technology used:&lt;br /&gt;
:* For &#039;&#039;&#039;FDM prints&#039;&#039;&#039;, supports are removed mechanically, and surfaces can be smoothed by light sanding or polishing.&lt;br /&gt;
:* For &#039;&#039;&#039;resin prints&#039;&#039;&#039;, supports are removed mechanically, parts are washed in isopropanol to remove uncured resin and then exposed to UV light for final curing.&lt;br /&gt;
:Models printed in multiple parts can be assembled using cyanoacrylate or epoxy adhesive. Optional finishing steps (painting, labeling) can improve contrast between subunits or highlight functional regions.&lt;br /&gt;
&lt;br /&gt;
==Generating printable files on Proteopedia==&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene, enabling logged-in users to effortlessly generate 3D-printable molecular models directly from its pages. The tool is powered by [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;], a script that analyzes the structural data and automatically scales the model’s geometry to match the printable volume of a medium-size desktop 3D printer (e.g., Ender-3, 210×210×210 mm). During this process, the tool evaluates the molecular bounding box, atom radii, and bond lengths, then proportionally adjusts all dimensions to achieve a realistic and mechanically robust print scale — preserving scientific accuracy while ensuring manufacturability. For advanced users, [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;] may also be used in conjunction with the [https://jmol.sourceforge.net/ &#039;&#039;&#039;Jmol&#039;&#039;&#039;] program, providing full access to its scripting capabilities and advanced export features.&lt;br /&gt;
==Step-by-step guide for automatic generation of printable files on Proteopedia==&lt;br /&gt;
=== Open a structure and access the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool ===&lt;br /&gt;
Log in with your Proteopedia Username and password. Navigate to any Proteopedia page (for example, [[Introduction_to_protein_structure]]). The corresponding 3D structure will load in the viewer on the right.  &lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_button_in_Proteopedia.png|thumb|left|400px|The &#039;&#039;&#039;Print3D&#039;&#039;&#039; button on a Proteopedia page]]&lt;br /&gt;
&lt;br /&gt;
At the bottom of the structure display window, locate and click the &#039;&#039;&#039;Print3D&#039;&#039;&#039; button. The tool will launch and begin analyzing the current molecular structure.  &lt;br /&gt;
This process may take some time to complete, depending on the size of the structure.  &lt;br /&gt;
Please wait until the message &#039;&#039;&#039;Analyzing structure...&#039;&#039;&#039; disappears and the next page is displayed — this marks the start of the two-step printing workflow.&lt;br /&gt;
=== Select a molecular representation and a printing scale ===&lt;br /&gt;
In this new page, some user input is required. Each option includes a short explanation; the key steps are outlined below, but feel free to explore and adopt the settings that best fit your use case.&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step1.png|thumb|left|400px|Selecting molecular representation and printing scale]]&lt;br /&gt;
&lt;br /&gt;
(1) &#039;&#039;&#039;Choose a molecular representation&#039;&#039;&#039; from the &#039;&#039;&#039;Scheme&#039;&#039;&#039; list, based on your goal:&lt;br /&gt;
* &#039;&#039;&#039;Backbone&#039;&#039;&#039;, &#039;&#039;&#039;Trace&#039;&#039;&#039;, or &#039;&#039;&#039;Ribbon&#039;&#039;&#039; — to emphasize secondary structure (effective for teaching protein folds).&lt;br /&gt;
* &#039;&#039;&#039;Surface&#039;&#039;&#039; — to highlight molecular topology and binding sites.&lt;br /&gt;
* &#039;&#039;&#039;Ball &amp;amp; Stick&#039;&#039;&#039; — atom-level detail for ligands or small molecules; usually impractical for large proteins or complexes.&lt;br /&gt;
* &#039;&#039;&#039;Proteopedia Scene&#039;&#039;&#039; — attempts to render the current page’s scene directly; may not work for all scenes. This is not fully implemented and only available for a few users.&lt;br /&gt;
&#039;&#039;Note:&#039;&#039; Some representations may be unavailable for a given structure because they are not printable in a reliable way.&lt;br /&gt;
&lt;br /&gt;
(2) In the &#039;&#039;&#039;Printer&#039;&#039;&#039; section, select whether you want a &#039;&#039;&#039;single-color&#039;&#039;&#039; or a &#039;&#039;&#039;multi-color&#039;&#039;&#039; print.&lt;br /&gt;
&lt;br /&gt;
(3) In the &#039;&#039;&#039;Printer scale&#039;&#039;&#039; section, set the desired size of the printed model. The tool constrains safe sizes based on the chosen representation and displays the physical dimensions (mm). &#039;&#039;&#039;Important! Please note the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;printer scale value in %&amp;lt;/span&amp;gt; as it is going to be required downstream in the next section of this workflow, [[#Printing files from Proteopedia|Printing files from Proteopedia]]&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
(4) When ready, click the green &#039;&#039;&#039;Make printer files&#039;&#039;&#039; button. Please wait patiently until the  &#039;&#039;Generating files for 3D printing of...&#039;&#039; message disappears and the final step is displayed.&lt;br /&gt;
&lt;br /&gt;
===Download the .STL or .OBJ files===&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step2.png|thumb|left|400px|Final step in generating printable files]]&lt;br /&gt;
&lt;br /&gt;
In this final page, a 3D preview of the generated model is displayed.&lt;br /&gt;
You can use the mouse to rotate, zoom, and inspect the model from different angles. If the result meets your needs, click the green (A) &#039;&#039;&#039;Download files&#039;&#039;&#039; button and save the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive containing the &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; files on your computer. If your model needs further improvements, hit the green (B) &#039;&#039;&#039;Same structure&#039;&#039;&#039; button to return to the previous screen and adjust your settings.&lt;br /&gt;
&lt;br /&gt;
 maybe a movie is better- need to decide ?&lt;br /&gt;
&lt;br /&gt;
{{clear}}&lt;br /&gt;
== Printing files from Proteopedia ==&lt;br /&gt;
Unzipping the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive will produce the exported &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file, along with an optional &#039;&#039;&#039;.MTL&#039;&#039;&#039; material file. &lt;br /&gt;
=== Using 3D printing services ===&lt;br /&gt;
If you do not have a 3D printer, you can still obtain physical models by using locally available 3D-printing services. Just search on [https://www.google.com/maps Google Maps] with the term  &#039;&#039;&#039;3D printing&#039;&#039;&#039; in your area. Here is short list of well-known 3D Printing service providers that may also ship worldwide: &lt;br /&gt;
&lt;br /&gt;
* [https://www.shapeways.com/ &#039;&#039;&#039;Shapeways&#039;&#039;&#039;] — global service offering a wide range of materials and colors. Educational discounts are available through their academic program.&lt;br /&gt;
* [https://www.sculpteo.com/en/ &#039;&#039;&#039;Sculpteo&#039;&#039;&#039;] — Europe-based provider offering fast turnaround and many printing technologies, including resin and polymer options.&lt;br /&gt;
* [https://www.xometry.com/capabilities/3d-printing-service &#039;&#039;&#039;Xometry&#039;&#039;&#039;] — large international network providing access to industrial-grade printing methods such as FDM, SLA, SLS, and DMLS.&lt;br /&gt;
* [https://craftcloud3d.com/ &#039;&#039;&#039;Craftcloud&#039;&#039;&#039;] — an aggregator that compares multiple providers and finds the best price and lead time for your uploaded model.&lt;br /&gt;
&lt;br /&gt;
When contacting a printing service, provide the exported files together with the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value in %&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ([[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). It is also advisable to share the link to this Proteopedia page so that the operator understands the peculiarities of printing molecular models. &lt;br /&gt;
&lt;br /&gt;
=== Using a desktop 3D printer ===&lt;br /&gt;
&lt;br /&gt;
Before importing the .STL or .OBJ file into your slicer software, it is recommended to inspect and, if necessary, repair the model to ensure printability. Common issues include non-manifold geometry, intersecting faces, and missing surfaces.  The example below demonstrates how to use [https://www.blender.org/ &#039;&#039;&#039;Blender&#039;&#039;&#039;] together with its [https://extensions.blender.org/add-ons/print3d-toolbox/ &#039;&#039;&#039;3D Print Toolbox extension&#039;&#039;&#039;] to improve the printability of the .STL and .OBJ files generated with the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in [[Proteopedia]]. &#039;&#039;&#039;Important note&#039;&#039;&#039;: The repair process is largely automated but may introduce artifacts. Carefully inspect the corrected model for any missing or distorted sections, atoms, or bonds, and determine whether these omissions affect the intended purpose of the printed model.  &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for single color or resin printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for multi-color FDM printing&lt;br /&gt;
|-&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=k6u-5JnoP-c&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=OCisrIZMIDM&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|}  &lt;br /&gt;
&lt;br /&gt;
Once the repaired &#039;&#039;&#039;.STL or .OBJ&#039;&#039;&#039; file is ready, it can be imported into your slicer software. In this step, you will prepare the file for printing by applying appropriate printer, filament, and print-settings profiles.&lt;br /&gt;
&lt;br /&gt;
*Apply the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value (%)&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ( [[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). This step ensures that the model fits your print bed and maintains structural integrity during printing. The location of the scale (%) input field varies depending on the slicer software you are using.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Orient the model on the print bed&#039;&#039;&#039; so that its largest, flattest surface rests on the bed. This minimizes the need for supports and improves adhesion. If your slicer includes an Auto Orient or Auto Arrange function, use it to optimize placement. (&#039;&#039;Hint&#039;&#039;: Bambu Studio and Orca Slicer include this feature, Ultimaker Cura has a [https://marketplace.ultimaker.com/app/cura/plugins/nallath/OrientationPlugin Auto-Orientation plugin] available, while PrusaSlicer currently does not.)&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Select the printer&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that matches your device.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Choose the material&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; corresponding to the filament type (e.g., PLA, PETG, TPU) and manufacturer you intend to use.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Adjust the printing parameters&#039;&#039;&#039; by selecting a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that defines layer height, infill, speed, and support options.&lt;br /&gt;
&lt;br /&gt;
In most cases, the default &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; and &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; provided by the slicer are sufficient. However, molecular models often include overhangs, thin connections, and complex internal geometries, which require additional supports and reinforced perimeters to ensure structural stability. For this reason, the default &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; may not yield optimal results.&lt;br /&gt;
&lt;br /&gt;
Validated printing profiles for the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool are available for several printer models. These profiles provide optimized settings that produce sturdy models, reduce material consumption, and shorten print time, ensuring consistent and reliable results. Three distinct profiles are supplied, corresponding to major molecular representations: &#039;&#039;&#039;balls and sticks&#039;&#039;&#039;, &#039;&#039;&#039;surface&#039;&#039;&#039;, and &#039;&#039;&#039;cartoon&#039;&#039;&#039;. The &#039;&#039;&#039;cartoon&#039;&#039;&#039; profile is also suitable for &#039;&#039;&#039;backbone&#039;&#039;&#039;, &#039;&#039;&#039;trace&#039;&#039;&#039;, and &#039;&#039;&#039;ribbon&#039;&#039;&#039; representations. For some printers, each profile is supplied in two variants, one using standard supports and one using tree or organic supports. In the case of multi-material printers, profiles for printing with soluble support and soluble interface are also provided.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer brand and model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Profiles provided as / Slicer&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer Type, nozle size and multi-material support&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |GitHub with profiles&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to import profiles into Slicer&lt;br /&gt;
|-&lt;br /&gt;
|Original Prusa Core One&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer ]&lt;br /&gt;
|FDM / 0.4 mm / yes, 5 colors, if MMU3 installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/Prusa%20CoreOne CoreOne]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab A1Mini&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, 4 colors if AMS Lite is installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/BambuLab%20A1Mini AiMini]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab X1 Carbon&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, up to 16 colors if multiple AMS are installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ca92e7de9c72505c1b9b09e912ad177341cabc9a/BambuLab%20X1C X1Carbon]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|- &lt;br /&gt;
|Original Prusa MK3S+&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/7a7ee68d1e19f063600f53def49a99dfefbc595d/Prusa%20MK3S%2B MK3S+]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 5 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/a653c7cc6b3dec86b90117cc450d1883cc4a80bd/Ender-5-Pro Ender5Pro]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 3 v2 with a ENDERIDEX kit&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / yes, IDEX, two filaments&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/c2c74f1261a42c160e7e3898a407f21465de2ca7/Ender3-IDEX Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Kingroon KPS3 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ea733b2d05020b99f91c92f71a039c5ba8e54108/Kingroon-KPS3-Pro Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Elegoo Mars 5 Ultra&lt;br /&gt;
|no profile needed, just be sure to add supports / [https://www.elegoo.com/pages/satellite-3d-slicer?srsltid=AfmBOopMQGHgHycHMFOZALzOIC8z7bVlSHjL_jj2ShYR4QkowYKmKzUx ELEGOO SatelLite]&lt;br /&gt;
|resin / - / no&lt;br /&gt;
|&lt;br /&gt;
|no profile needed, default settings worked, just be sure to add supports. EVO supports worked well enough.  Post-processing steps: 1)washing: at least 10 min. 2) support removal 3)curring: at least 10 min on a Elegoo Mercury Plus V3.0&lt;br /&gt;
|- &lt;br /&gt;
|} &lt;br /&gt;
&#039;&#039;&#039;Notes&#039;&#039;&#039;: &lt;br /&gt;
* These profiles were developed and validated with the support of EDUMOL3D, Project [http://cercetare.bio.uaic.ro/grupuri/bioactive/content/grants/PED2024_mm.html PN-IV-P7-7.1-PED-2024-0343] financed by the Ministry of Research, Innovation and Digitization, [https://uefiscdi.gov.ro/ UEFISCDI], Romania.&lt;br /&gt;
* The profiles are a work in progress. Please check GitHub for updates. If you have suggestions for improvements, please drop a message at marius.mihasan(@)uaic.ro&lt;br /&gt;
&lt;br /&gt;
==== &#039;&#039;&#039;Note on multi-color printing &#039;&#039;&#039; ====&lt;br /&gt;
To our knowledge, only &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039; and &#039;&#039;&#039;Orca Slicer&#039;&#039;&#039; can automatically import color information from the &#039;&#039;&#039;.MTL&#039;&#039;&#039; file associated with the printable &#039;&#039;&#039;.OBJ&#039;&#039;&#039; generated by the Proteopedia &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool.  &lt;br /&gt;
At present, &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; does not support importing &#039;&#039;&#039;.MTL&#039;&#039;&#039; files directly.&lt;br /&gt;
&lt;br /&gt;
A practical workaround for &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; users is as follows:  &lt;br /&gt;
# Open the &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file in &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039;.  &lt;br /&gt;
#Verify or adjust the color mapping as needed.  &lt;br /&gt;
#Export the model as a generic &#039;&#039;&#039;.3MF&#039;&#039;&#039; file using the menu command:  &#039;&#039;File&#039;&#039; → &#039;&#039;Export&#039;&#039; → &#039;&#039;Export Generic 3MF...&#039;&#039;  &lt;br /&gt;
#Open the exported &#039;&#039;&#039;.3MF&#039;&#039;&#039; file in &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;. The color data will now be available under the &#039;&#039;&#039;Multimaterial Painting&#039;&#039;&#039; tool.&lt;br /&gt;
&lt;br /&gt;
This workflow preserves the original coloring assigned in Proteopedia and allows successful multi-color or multi-material printing on any capable 3D printer compatible with &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Other relevant resources ==&lt;br /&gt;
[[User:Marius_Mihasan/Print3D_models_gallery]] - examples of 3D printed molecular models from Proteopedia users.&lt;br /&gt;
&lt;br /&gt;
[https://3d.nih.gov/ NIH 3D Print Exchange] - an open, community-driven portal to download, share, and create bioscientific and medical 3D models, including for 3D printing.&lt;br /&gt;
  &lt;br /&gt;
[https://github.com/mariusmihasan/3DP-Jmol 3DP-Jmol] - the Jmol/JSmol behind the Print3D tool. Automatically generates 3D printable molecular models from structural data and can be easily integrated into web pages.&lt;br /&gt;
&lt;br /&gt;
[https://pdb101.rcsb.org/learn/3d-printing/pdb-structures-and-3d-printing 3D Printing on PDB101] - a quick guide on 3D printing molecular models and a small curated 3D models for education&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;If you print a model from Proteopedia, please share photos and feedback — let’s 3D print the whole Proteopedia!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386107</id>
		<title>Print3D help</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386107"/>
		<updated>2025-10-27T10:05:21Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== Proteopedia and 3D Printing ==&lt;br /&gt;
&lt;br /&gt;
Physical molecular models, by engaging both visual and tactile senses, provide an effective means of deepening the understanding of complex concepts in molecular biology and biochemistry. They allow students to perceive the three-dimensional organization of macromolecules, thereby enhancing comprehension of the relationship between structure and function &amp;lt;ref&amp;gt;PMID: 32590880&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 40214166&amp;lt;/ref&amp;gt;. Numerous studies have demonstrated that the use of tangible models in science education improves learning outcomes, fosters conceptual reasoning, and increases student engagement &amp;lt;ref&amp;gt;PMID: 27366318&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 26712513&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;Larsson, C., Tibell, L.A.E. Challenging Students’ Intuitions—the Influence of a Tangible Model of Virus Assembly on Students’ Conceptual Reasoning About the Process of Self-Assembly. Res Sci Educ 45, 663–690 (2015). [http://dx.doi.org/10.1007/s11165-014-9446-6 DOI: 110.1007/s11165-014-9446-6]&amp;lt;/ref&amp;gt;. The rapid development of 3D-printing technologies has made it possible to create customized and affordable molecular models  &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot;&amp;gt;PMID: 28362403&amp;lt;/ref&amp;gt; &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot;&amp;gt;PMID: 33755300&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 33384761&amp;lt;/ref&amp;gt;. &lt;br /&gt;
&lt;br /&gt;
Affordable desktop 3D printers can now be used to fabricate physical models from virtually any structure or scene on [[Proteopedia]]. This page provides an introduction to 3D printing, a step-by-step guide to generating printable files directly from [[Proteopedia]], and several tested printing profiles for common printers (e.g., Prusa Research, Bambu Lab, Creality, or Elegoo).&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== «3D Printing 101»: an introduction to 3D printing ==&lt;br /&gt;
3D printing, also known as &#039;&#039;additive manufacturing&#039;&#039;, builds physical objects layer by layer from digital designs. For more technical details please head for the excellent introductory article on [https://all3dp.com/2/what-is-3d-printing/ All3DP].  In structural biology education, 3D printing provides an affordable and accessible way to transform atomic coordinate data (e.g., from PDB, MOL or SDF files) into tangible molecular models that can be observed, handled, and discussed in class or laboratory settings.&lt;br /&gt;
&lt;br /&gt;
=== Printer Types: FDM vs. SLA/DLP ===&lt;br /&gt;
The two most accessible 3D-printing technologies that can be used to create molecular models are:&lt;br /&gt;
* &#039;&#039;&#039;FDM (Fused Deposition Modeling)&#039;&#039;&#039;&lt;br /&gt;
This method extrudes a heated thermoplastic filament (such as PLA, PETG or TPU) through a fine nozzle, depositing successive layers that form the model. FDM printers have the advantages of low cost, easy maintenance, wide availability, and being capable of printing large and colorful molecular models. This technology has a few limitations, such as: visible layer lines, lower surface resolution, and less suited for very small or intricate molecular details.&lt;br /&gt;
* &#039;&#039;&#039;SLA/DLP (Resin Printing)&#039;&#039;&#039;&lt;br /&gt;
This technique uses liquid photopolymer resin, cured layer by layer with ultraviolet light. SLA/DLP printers have the advantages of a very high resolution, smooth surfaces and are ideal for compact and detailed models (e.g., small proteins rendered as surface, ligands, or symmetric assemblies). This technology has its own limitations, such as higher material cost, post-processing requirements (washing and UV-curing), and the need for careful handling of resin.&lt;br /&gt;
&lt;br /&gt;
When choosing between FDM and SLA printers, model size and resolution are the key criteria: &#039;&#039;&#039;FDM&#039;&#039;&#039; is preferred for &#039;&#039;large, educational display models&#039;&#039;; &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; is optimal for &#039;&#039;small, precise structures&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
While FDM and SLA/DLP are the most widely used technologies in educational and research contexts due to their accessibility, other additive manufacturing methods also exist —such as &#039;&#039;Selective Laser Sintering&#039;&#039; (SLS), &#039;&#039;PolyJet&#039;&#039;, and &#039;&#039;Binder Jetting&#039;&#039;— each employing different materials and curing mechanisms. These industrial-grade techniques can produce highly detailed or multi-material parts but are generally more expensive and less accessible for classroom use. For an overview of major 3D-printing technologies, see [https://all3dp.com/1/types-of-3d-printers-3d-printing-technology/ All3DP: Complete Overview of the Types of 3D Printers]&lt;br /&gt;
&lt;br /&gt;
=== Single- vs. Multi-Material Printers ===&lt;br /&gt;
Most entry-level desktop 3D printers use a single filament or resin, producing models in one color or material. However, multi-material systems (such as [https://eu.store.bambulab.com/products/ams-multicolor-printing?from=home_web_top_navigation Bambu Lab AMS] and its variants or [https://www.prusa3d.com/category/original-prusa-mmu3/ Prusa MMU3]) can simultaneously print multiple filaments, enabling color-coded domains, subunits, or ligands directly in one print. For complex color information, users can also apply post-print color coding (painting or labeling) or print separate parts and assemble them manually.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A large FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A multi-material FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Small resin-printed models&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:GABAA_receptor.png|320px|center|thumb| GABAA receptor, [[6x3x]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Bacterial_Ribosome_multimaterial_FDM.png|348px|center|thumb| Bacterial 70S ribosome, [[4v5d]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Dna_insuline_sla.png|252px|center|thumb|DNA (left) and insulin (right) models, [[4bna]] and [[4ins]], scale at the bottom in cm]]&lt;br /&gt;
|-&lt;br /&gt;
|Trace Model of the GABAA receptor printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com] &lt;br /&gt;
|Surface model of the Bacterial 70S ribosome printed on a multi-material capable printer (BambuLab X1C AMS). Blue and violet are ribosomal proteins, orange and yellow are rRNAs, and black is tRNA. Printable files available on [https://www.printables.com/model/1430877-bacterial-70s-ribosome Printables.com]&lt;br /&gt;
|Balls and sticks and cartoon models of DNA (right) and insulin (left)&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== File Formats Used in 3D Printing ===&lt;br /&gt;
Proteopedia supports two export formats for generating printable molecular models:&lt;br /&gt;
*&#039;&#039;&#039;.STL&#039;&#039;&#039; (Stereolithography): the most common and universally compatible format; encodes only surface geometry, without color or texture information.&lt;br /&gt;
*&#039;&#039;&#039;.OBJ&#039;&#039;&#039; (Wavefront Object) with an associated &#039;&#039;&#039;.MTL&#039;&#039;&#039; (Material Template Library) files: includes both geometry and optional color/texture data; useful for color prints.&lt;br /&gt;
&lt;br /&gt;
Another widely adopted file format used in 3D printing is the &#039;&#039;&#039;.3MF&#039;&#039;&#039; (3D Manufacturing Format): a modern open standard that stores geometry, color, and multi-material metadata in a single file—recommended for advanced printers. For a more extensive pros and cons of different 3D printing file formats please see [https://all3dp.com/2/3d-file-format-3d-model-types/ The Main 3D Printing File Formats on all3dp]. &lt;br /&gt;
&lt;br /&gt;
STL is ideal for single-color models and maximum compatibility, while OBJ/MTL is recommended for multi-material workflows. 3MF files will be used in this tutorial to save the model and printing settings. &lt;br /&gt;
&lt;br /&gt;
Support in Proteopedia for these formats is based on the export capabilities of Jmol/JSmol; for details, see [http://wiki.jmol.org/index.php/File_formats/3D_Objects#STL STL] and [http://wiki.jmol.org/index.php/File_formats/3D_Objects#OBJ OBJ]&lt;br /&gt;
&lt;br /&gt;
== Overview of the 3D printing process ==&lt;br /&gt;
3D printing enables the transformation of atomic-level structural data into tangible macromolecular models that can be explored through both sight and touch.  &lt;br /&gt;
The process generally follows several main steps, each requiring specific types of software and hardware.&lt;br /&gt;
[[Image:3D_printing_workflow_v2.png|thumb|left|400px|Overview of the 3D printing workflow for generating physical molecular models.]]&lt;br /&gt;
	&lt;br /&gt;
=== Preparing the structure and generating a printable File ===&lt;br /&gt;
:The first stage involves creating a printable three-dimensional representation of the molecule. Some molecular-graphics programs such as [https://www.pymol.org/ PyMOL], [https://www.rbvi.ucsf.edu/chimerax/ UCSF ChimeraX], [https://molstar.org/Mol*], or [https://jmol.sourceforge.net/ Jmol] can be used not only to visualize a structure (from the Protein Data Bank or other sources), but also to export the resulting geometry in a .STL or .OBJ format. However, the default visualization styles of these programs are &#039;&#039;&#039;&#039;&#039;not directly suitable for 3D printing&#039;&#039;&#039;&#039;&#039;. Therefore, when preparing a model for fabrication, it is important to:&lt;br /&gt;
:* &#039;&#039;&#039;Select an appropriate molecular representation&#039;&#039;&#039; (e.g., surface, cartoon, sticks, spheres) depending on the pedagogical or structural feature you wish to highlight.  &lt;br /&gt;
:* &#039;&#039;&#039;Add struts or connectors&#039;&#039;&#039; to increase the mechanical stability of the model, especially for large complexes or long helices.  &lt;br /&gt;
:* &#039;&#039;&#039;Remove specific struts or pseudobonds&#039;&#039;&#039; when individual components — ligands, subunits, or cofactors — need to remain detachable.  &lt;br /&gt;
:* &#039;&#039;&#039;Adjust thickness&#039;&#039;&#039; of atoms, bonds, helices, and sheets to ensure adequate rigidity and printability (features thinner than the printer’s nozzle diameter or resin resolution may break).  &lt;br /&gt;
:* &#039;&#039;&#039;Apply meaningful coloring&#039;&#039;&#039; when preparing multi-material prints, for instance, to distinguish domains, chains, ligands or atoms.&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene that automates the process and enables users to effortlessly generate 3D-printable molecular models - more on that in the corresponding section [[#Generating printable files on Proteopedia|Generating printable files on Proteopedia]] within this page. For advanced users wanting to do this manually, we highly recommend two guides: &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot; /&amp;gt; and &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
=== Slicing the Model ===&lt;br /&gt;
Before printing, the STL file must be processed by a &#039;&#039;&#039;slicer&#039;&#039;&#039; — specialized software that converts 3D geometry into a series of horizontal layers. The slicer also generates &#039;&#039;&#039;G-code&#039;&#039;&#039;, the set of instructions that control the printer. These commands are printer-specific and include parameters such as extrusion speed, layer thickness, temperature, and movement. Together, they are usually stored as a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;.  &lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an FDM printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;number of perimeters&#039;&#039;&#039;, which affects mechanical strength and print time;&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines resolution and print duration;&lt;br /&gt;
:* &#039;&#039;&#039;infill density&#039;&#039;&#039;, which determines internal strength and affects print time;&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, temporary structures that hold overhanging regions;&lt;br /&gt;
:* &#039;&#039;&#039;print orientation&#039;&#039;&#039;, which influences surface quality, mechanical strength, and the amount of supports required.&lt;br /&gt;
:All these parameters make up a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. In this step, users must also select the material-specific parameters, or apply a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. More details on these profiles are provided later on this page.&lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines vertical resolution and print time; thinner layers produce smoother surfaces but significantly increase printing duration.&lt;br /&gt;
:* &#039;&#039;&#039;exposure time&#039;&#039;&#039;, which controls how long each layer is cured by UV light; optimal exposure ensures proper adhesion between layers without over-curing fine details.&lt;br /&gt;
:* &#039;&#039;&#039;bottom-layer exposure and count&#039;&#039;&#039;, which influence model adhesion to the build platform — longer exposures and additional base layers improve stability during printing.&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, which anchor the model to the build plate and prevent deformation during peeling; proper placement reduces surface marks and print failures.&lt;br /&gt;
:* &#039;&#039;&#039;model orientation&#039;&#039;&#039;, which affects surface quality, support contact area, and resin drainage; angling the model (typically 30–45°) minimizes suction forces and improves print reliability.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for FDM printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for resin printing&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:Insuline_sliced_prusa.gif|386px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|[[Image:Insuline_Sliced_SLA.gif|372px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|-&lt;br /&gt;
|Cartoon model of insulin sliced in PrusaSlicer and ready to be printed on FDM printers. The arrow shows the trajectory of the print head on a single slice or layer. Orange is the model, green are the supports. &lt;br /&gt;
|Cartoon model of insulin sliced in Elegoo SatelLite and ready to be printed on FDM printer.On the left, with blue is the model, with gray are the supports. On the right is the image on the UV screen. &lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== 3D Printing the Model ===&lt;br /&gt;
:The prepared G-code is then transferred to the 3D printer, either via an SD card, USB flash drive, or Wi-Fi connection. During printing, close observation of the first few layers is essential to ensure good adhesion to the build plate and a successful print. Total printing time depends on model size, selected layer height, and printer speed. &#039;&#039;Small peptide&#039;&#039; models may print in &#039;&#039;&#039;less than an hour&#039;&#039;&#039;, whereas l&#039;&#039;arge multimeric assemblies&#039;&#039; can require &#039;&#039;&#039;several hours or days&#039;&#039;&#039;. &#039;&#039;Multi-color&#039;&#039; or &#039;&#039;multi-material&#039;&#039; prints generally take &#039;&#039;&#039;longer&#039;&#039;&#039;, while &#039;&#039;SLA/DLP&#039;&#039; printers are generally &#039;&#039;&#039;faster&#039;&#039;&#039; due to their simultaneous layer exposure.&lt;br /&gt;
=== Post-Processing ===&lt;br /&gt;
:After printing, the model undergoes post-processing, which varies depending on the printing technology used:&lt;br /&gt;
:* For &#039;&#039;&#039;FDM prints&#039;&#039;&#039;, supports are removed mechanically, and surfaces can be smoothed by light sanding or polishing.&lt;br /&gt;
:* For &#039;&#039;&#039;resin prints&#039;&#039;&#039;, supports are removed mechanically, parts are washed in isopropanol to remove uncured resin and then exposed to UV light for final curing.&lt;br /&gt;
:Models printed in multiple parts can be assembled using cyanoacrylate or epoxy adhesive. Optional finishing steps (painting, labeling) can improve contrast between subunits or highlight functional regions.&lt;br /&gt;
&lt;br /&gt;
==Generating printable files on Proteopedia==&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene, enabling logged users to effortlessly generate 3D-printable molecular models directly from its pages. The tool is powered by [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;], a script that analyzes the structural data and automatically scales the model’s geometry to match the printable volume of a medium-size desktop 3D printer (e.g., Ender-3, 210×210×210 mm). During this process, the tool evaluates the molecular bounding box, atom radii, and bond lengths, then proportionally adjusts all dimensions to achieve a realistic and mechanically robust print scale — preserving scientific accuracy while ensuring manufacturability. For advanced users, [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;] may also be used in conjunction with the [https://jmol.sourceforge.net/ &#039;&#039;&#039;Jmol&#039;&#039;&#039;] program, providing full access to its scripting capabilities and advanced export features.&lt;br /&gt;
==Step-by-step guide for automatic generation of printable files on Proteopedia==&lt;br /&gt;
=== Open a structure and access the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool ===&lt;br /&gt;
Log in with your Proteopedia Username and password. Navigate to any Proteopedia page (for example, [[Introduction_to_protein_structure]]). The corresponding 3D structure will load in the viewer on the right.  &lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_button_in_Proteopedia.png|thumb|left|400px|The &#039;&#039;&#039;Print3D&#039;&#039;&#039; button on a Proteopedia page]]&lt;br /&gt;
&lt;br /&gt;
At the bottom of the structure display window, locate and click the &#039;&#039;&#039;Print3D&#039;&#039;&#039; button. The tool will launch and begin analyzing the current molecular structure.  &lt;br /&gt;
This process may take some time to complete, depending on the size of the structure.  &lt;br /&gt;
Please wait until the message &#039;&#039;&#039;Analyzing structure...&#039;&#039;&#039; disappears and the next page is displayed — this marks the start of the two-step printing workflow.&lt;br /&gt;
=== Select a molecular representation and a printing scale ===&lt;br /&gt;
In this new page, some user input is required. Each option includes a short explanation; the key steps are outlined below, but feel free to explore and adopt the settings that best fit your use case.&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step1.png|thumb|left|400px|Selecting molecular representation and printing scale]]&lt;br /&gt;
&lt;br /&gt;
(1) &#039;&#039;&#039;Choose a molecular representation&#039;&#039;&#039; from the &#039;&#039;&#039;Scheme&#039;&#039;&#039; list, based on your goal:&lt;br /&gt;
* &#039;&#039;&#039;Backbone&#039;&#039;&#039;, &#039;&#039;&#039;Trace&#039;&#039;&#039;, or &#039;&#039;&#039;Ribbon&#039;&#039;&#039; — to emphasize secondary structure (effective for teaching protein folds).&lt;br /&gt;
* &#039;&#039;&#039;Surface&#039;&#039;&#039; — to highlight molecular topology and binding sites.&lt;br /&gt;
* &#039;&#039;&#039;Ball &amp;amp; Stick&#039;&#039;&#039; — atom-level detail for ligands or small molecules; usually impractical for large proteins or complexes.&lt;br /&gt;
* &#039;&#039;&#039;Proteopedia Scene&#039;&#039;&#039; — attempts to render the current page’s scene directly; may not work for all scenes. This is not fully implemented and only available for a few users.&lt;br /&gt;
&#039;&#039;Note:&#039;&#039; Some representations may be unavailable for a given structure because they are not printable in a reliable way.&lt;br /&gt;
&lt;br /&gt;
(2) In the &#039;&#039;&#039;Printer&#039;&#039;&#039; section, select whether you want a &#039;&#039;&#039;single-color&#039;&#039;&#039; or a &#039;&#039;&#039;multi-color&#039;&#039;&#039; print.&lt;br /&gt;
&lt;br /&gt;
(3) In the &#039;&#039;&#039;Printer scale&#039;&#039;&#039; section, set the desired size of the printed model. The tool constrains safe sizes based on the chosen representation and displays the physical dimensions (mm). &#039;&#039;&#039;Important! Please note the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;printer scale value in %&amp;lt;/span&amp;gt; as it is going to be required downstream in the next section of this workflow, [[#Printing files from Proteopedia|Printing files from Proteopedia]]&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
(4) When ready, click the green &#039;&#039;&#039;Make printer files&#039;&#039;&#039; button. Please wait patiently until the  &#039;&#039;Generating files for 3D printing of...&#039;&#039; message disappears and the final step is displayed.&lt;br /&gt;
&lt;br /&gt;
===Download the .STL or .OBJ files===&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step2.png|thumb|left|400px|Final step in generating printable files]]&lt;br /&gt;
&lt;br /&gt;
In this final page, a 3D preview of the generated model is displayed.&lt;br /&gt;
You can use the mouse to rotate, zoom, and inspect the model from different angles. If the result meets your needs, click the green (A) &#039;&#039;&#039;Download files&#039;&#039;&#039; button and save the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive containing the &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; files on your computer. If your model needs further improvements, hit the green (B) &#039;&#039;&#039;Same structure&#039;&#039;&#039; button to return to the previous screen and adjust your settings.&lt;br /&gt;
&lt;br /&gt;
 maybe a movie is better- need to decide ?&lt;br /&gt;
&lt;br /&gt;
{{clear}}&lt;br /&gt;
== Printing files from Proteopedia ==&lt;br /&gt;
Unzipping the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive will produce the exported &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file, along with an optional &#039;&#039;&#039;.MTL&#039;&#039;&#039; material file. &lt;br /&gt;
=== Using 3D printing services ===&lt;br /&gt;
If you do not have a 3D printer, you can still obtain physical models by using locally available 3D-printing services. Just search on [https://www.google.com/maps Google Maps] with the term  &#039;&#039;&#039;3D printing&#039;&#039;&#039; in your area. Here is short list of well-known 3D Printing service providers that may also ship worldwide: &lt;br /&gt;
&lt;br /&gt;
* [https://www.shapeways.com/ &#039;&#039;&#039;Shapeways&#039;&#039;&#039;] — global service offering a wide range of materials and colors. Educational discounts are available through their academic program.&lt;br /&gt;
* [https://www.sculpteo.com/en/ &#039;&#039;&#039;Sculpteo&#039;&#039;&#039;] — Europe-based provider offering fast turnaround and many printing technologies, including resin and polymer options.&lt;br /&gt;
* [https://www.xometry.com/capabilities/3d-printing-service &#039;&#039;&#039;Xometry&#039;&#039;&#039;] — large international network providing access to industrial-grade printing methods such as FDM, SLA, SLS, and DMLS.&lt;br /&gt;
* [https://craftcloud3d.com/ &#039;&#039;&#039;Craftcloud&#039;&#039;&#039;] — an aggregator that compares multiple providers and finds the best price and lead time for your uploaded model.&lt;br /&gt;
&lt;br /&gt;
When contacting a printing service, provide the exported files together with the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value in %&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ([[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). It is also advisable to share the link to this Proteopedia page so that the operator understands the peculiarities of printing molecular models. &lt;br /&gt;
&lt;br /&gt;
=== Using a desktop 3D printer ===&lt;br /&gt;
&lt;br /&gt;
Before importing the .STL or .OBJ file into your slicer software, it is recommended to inspect and, if necessary, repair the model to ensure printability. Common issues include non-manifold geometry, intersecting faces, and missing surfaces.  The example below demonstrates how to use [https://www.blender.org/ &#039;&#039;&#039;Blender&#039;&#039;&#039;] together with its [https://extensions.blender.org/add-ons/print3d-toolbox/ &#039;&#039;&#039;3D Print Toolbox extension&#039;&#039;&#039;] to improve the printability of the .STL and .OBJ files generated with the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in [[Proteopedia]]. &#039;&#039;&#039;Important note&#039;&#039;&#039;: The repair process is largely automated but may introduce artifacts. Carefully inspect the corrected model for any missing or distorted sections, atoms, or bonds, and determine whether these omissions affect the intended purpose of the printed model.  &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for single color or resin printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for multi-color FDM printing&lt;br /&gt;
|-&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=k6u-5JnoP-c&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=OCisrIZMIDM&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|}  &lt;br /&gt;
&lt;br /&gt;
Once the repaired &#039;&#039;&#039;.STL or .OBJ&#039;&#039;&#039; file is ready, it can be imported into your slicer software. In this step, you will prepare the file for printing by applying appropriate printer, filament, and print-settings profiles.&lt;br /&gt;
&lt;br /&gt;
*Apply the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value (%)&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ( [[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). This step ensures that the model fits your print bed and maintains structural integrity during printing. The location of the scale (%) input field varies depending on the slicer software you are using.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Orient the model on the print bed&#039;&#039;&#039; so that its largest, flattest surface rests on the bed. This minimizes the need for supports and improves adhesion. If your slicer includes an Auto Orient or Auto Arrange function, use it to optimize placement. (&#039;&#039;Hint&#039;&#039;: Bambu Studio and Orca Slicer include this feature, Ultimaker Cura has a [https://marketplace.ultimaker.com/app/cura/plugins/nallath/OrientationPlugin Auto-Orientation plugin] available, while PrusaSlicer currently does not.)&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Select the printer&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that matches your device.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Choose the material&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; corresponding to the filament type (e.g., PLA, PETG, TPU) and manufacturer you intend to use.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Adjust the printing parameters&#039;&#039;&#039; by selecting a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that defines layer height, infill, speed, and support options.&lt;br /&gt;
&lt;br /&gt;
In most cases, the default &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; and &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; provided by the slicer are sufficient. However, molecular models often include overhangs, thin connections, and complex internal geometries, which require additional supports and reinforced perimeters to ensure structural stability. For this reason, the default &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; may not yield optimal results.&lt;br /&gt;
&lt;br /&gt;
Validated printing profiles for the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool are available for several printer models. These profiles provide optimized settings that produce sturdy models, reduce material consumption, and shorten print time, ensuring consistent and reliable results. Three distinct profiles are supplied, corresponding to major molecular representations: &#039;&#039;&#039;balls and sticks&#039;&#039;&#039;, &#039;&#039;&#039;surface&#039;&#039;&#039;, and &#039;&#039;&#039;cartoon&#039;&#039;&#039;. The &#039;&#039;&#039;cartoon&#039;&#039;&#039; profile is also suitable for &#039;&#039;&#039;backbone&#039;&#039;&#039;, &#039;&#039;&#039;trace&#039;&#039;&#039;, and &#039;&#039;&#039;ribbon&#039;&#039;&#039; representations. For some printers, each profile is supplied in two variants, one using standard supports and one using tree or organic supports. In the case of multi-material printers, profiles for printing with soluble support and soluble interface are also provided.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer brand and model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Profiles provided as / Slicer&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer Type, nozle size and multi-material support&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |GitHub with profiles&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to import profiles into Slicer&lt;br /&gt;
|-&lt;br /&gt;
|Original Prusa Core One&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer ]&lt;br /&gt;
|FDM / 0.4 mm / yes, 5 colors, if MMU3 installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/Prusa%20CoreOne CoreOne]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab A1Mini&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, 4 colors if AMS Lite is installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/BambuLab%20A1Mini AiMini]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab X1 Carbon&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, up to 16 colors if multiple AMS are installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ca92e7de9c72505c1b9b09e912ad177341cabc9a/BambuLab%20X1C X1Carbon]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|- &lt;br /&gt;
|Original Prusa MK3S+&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/7a7ee68d1e19f063600f53def49a99dfefbc595d/Prusa%20MK3S%2B MK3S+]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 5 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/a653c7cc6b3dec86b90117cc450d1883cc4a80bd/Ender-5-Pro Ender5Pro]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 3 v2 with a ENDERIDEX kit&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / yes, IDEX, two filaments&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/c2c74f1261a42c160e7e3898a407f21465de2ca7/Ender3-IDEX Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Kingroon KPS3 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ea733b2d05020b99f91c92f71a039c5ba8e54108/Kingroon-KPS3-Pro Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Elegoo Mars 5 Ultra&lt;br /&gt;
|no profile needed, just be sure to add supports / [https://www.elegoo.com/pages/satellite-3d-slicer?srsltid=AfmBOopMQGHgHycHMFOZALzOIC8z7bVlSHjL_jj2ShYR4QkowYKmKzUx ELEGOO SatelLite]&lt;br /&gt;
|resin / - / no&lt;br /&gt;
|&lt;br /&gt;
|no profile needed, default settings worked, just be sure to add supports. EVO supports worked well enough.  Post-processing steps: 1)washing: at least 10 min. 2) support removal 3)curring: at least 10 min on a Elegoo Mercury Plus V3.0&lt;br /&gt;
|- &lt;br /&gt;
|} &lt;br /&gt;
&#039;&#039;&#039;Notes&#039;&#039;&#039;: &lt;br /&gt;
* These profiles were developed and validated with the support of EDUMOL3D, Project [http://cercetare.bio.uaic.ro/grupuri/bioactive/content/grants/PED2024_mm.html PN-IV-P7-7.1-PED-2024-0343] financed by the Ministry of Research, Innovation and Digitization, [https://uefiscdi.gov.ro/ UEFISCDI], Romania.&lt;br /&gt;
* The profiles are a work in progress. Please check GitHub for updates. If you have suggestions for improvements, please drop a message at marius.mihasan(@)uaic.ro&lt;br /&gt;
&lt;br /&gt;
==== &#039;&#039;&#039;Note on multi-color printing &#039;&#039;&#039; ====&lt;br /&gt;
To our knowledge, only &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039; and &#039;&#039;&#039;Orca Slicer&#039;&#039;&#039; can automatically import color information from the &#039;&#039;&#039;.MTL&#039;&#039;&#039; file associated with the printable &#039;&#039;&#039;.OBJ&#039;&#039;&#039; generated by the Proteopedia &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool.  &lt;br /&gt;
At present, &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; does not support importing &#039;&#039;&#039;.MTL&#039;&#039;&#039; files directly.&lt;br /&gt;
&lt;br /&gt;
A practical workaround for &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; users is as follows:  &lt;br /&gt;
# Open the &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file in &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039;.  &lt;br /&gt;
#Verify or adjust the color mapping as needed.  &lt;br /&gt;
#Export the model as a generic &#039;&#039;&#039;.3MF&#039;&#039;&#039; file using the menu command:  &#039;&#039;File&#039;&#039; → &#039;&#039;Export&#039;&#039; → &#039;&#039;Export Generic 3MF...&#039;&#039;  &lt;br /&gt;
#Open the exported &#039;&#039;&#039;.3MF&#039;&#039;&#039; file in &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;. The color data will now be available under the &#039;&#039;&#039;Multimaterial Painting&#039;&#039;&#039; tool.&lt;br /&gt;
&lt;br /&gt;
This workflow preserves the original coloring assigned in Proteopedia and allows successful multi-color or multi-material printing on any capable 3D printer compatible with &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Other relevant resources ==&lt;br /&gt;
[[User:Marius_Mihasan/Print3D_models_gallery]] - examples of 3D printed molecular models from Proteopedia users.&lt;br /&gt;
&lt;br /&gt;
[https://3d.nih.gov/ NIH 3D Print Exchange] - an open, community-driven portal to download, share, and create bioscientific and medical 3D models, including for 3D printing.&lt;br /&gt;
  &lt;br /&gt;
[https://github.com/mariusmihasan/3DP-Jmol 3DP-Jmol] - the Jmol/JSmol behind the Print3D tool. Automatically generates 3D printable molecular models from structural data and can be easily integrated into web pages.&lt;br /&gt;
&lt;br /&gt;
[https://pdb101.rcsb.org/learn/3d-printing/pdb-structures-and-3d-printing 3D Printing on PDB101] - a quick guide on 3D printing molecular models and a small curated 3D models for education&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;If you print a model from Proteopedia, please share photos and feedback — let’s 3D print the whole Proteopedia!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386106</id>
		<title>Print3D help</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386106"/>
		<updated>2025-10-27T10:04:42Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== Proteopedia and 3D Printing ==&lt;br /&gt;
&lt;br /&gt;
Physical molecular models, by engaging both visual and tactile senses, provide an effective means of deepening the understanding of complex concepts in molecular biology and biochemistry. They allow students to perceive the three-dimensional organization of macromolecules, thereby enhancing comprehension of the relationship between structure and function &amp;lt;ref&amp;gt;PMID: 32590880&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 40214166&amp;lt;/ref&amp;gt;. Numerous studies have demonstrated that the use of tangible models in science education improves learning outcomes, fosters conceptual reasoning, and increases student engagement &amp;lt;ref&amp;gt;PMID: 27366318&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 26712513&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;Larsson, C., Tibell, L.A.E. Challenging Students’ Intuitions—the Influence of a Tangible Model of Virus Assembly on Students’ Conceptual Reasoning About the Process of Self-Assembly. Res Sci Educ 45, 663–690 (2015). [http://dx.doi.org/10.1007/s11165-014-9446-6 DOI: 110.1007/s11165-014-9446-6]&amp;lt;/ref&amp;gt;. The rapid development of 3D-printing technologies has made it possible to create customized and affordable molecular models  &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot;&amp;gt;PMID: 28362403&amp;lt;/ref&amp;gt; &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot;&amp;gt;PMID: 33755300&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 33384761&amp;lt;/ref&amp;gt;. &lt;br /&gt;
&lt;br /&gt;
Affordable desktop 3D printers can now be used to fabricate physical models from virtually any structure or scene on [[Proteopedia]]. This page provides an introduction to 3D printing, a step-by-step guide to generating printable files directly from [[Proteopedia]], and several tested printing profiles for common printers (e.g., Prusa Research, Bambu Lab, Creality, or Elegoo).&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== «3D Printing 101»: an introduction to 3D printing ==&lt;br /&gt;
3D printing, also known as &#039;&#039;additive manufacturing&#039;&#039;, builds physical objects layer by layer from digital designs. For more technical details please head for the excellent introductory article on [https://all3dp.com/2/what-is-3d-printing/ All3DP].  In structural biology education, 3D printing provides an affordable and accessible way to transform atomic coordinate data (e.g., from PDB, MOL or SDF files) into tangible molecular models that can be observed, handled, and discussed in class or laboratory settings.&lt;br /&gt;
&lt;br /&gt;
=== Printer Types: FDM vs. SLA/DLP ===&lt;br /&gt;
The two most accessible 3D-printing technologies that can be used to create molecular models are:&lt;br /&gt;
* &#039;&#039;&#039;FDM (Fused Deposition Modeling)&#039;&#039;&#039;&lt;br /&gt;
This method extrudes a heated thermoplastic filament (such as PLA, PETG or TPU) through a fine nozzle, depositing successive layers that form the model. FDM printers have the advantages of low cost, easy maintenance, wide availability, and being capable of printing large and colorful molecular models. This technology has a few limitations, such as: visible layer lines, lower surface resolution, and less suited for very small or intricate molecular details.&lt;br /&gt;
* &#039;&#039;&#039;SLA/DLP (Resin Printing)&#039;&#039;&#039;&lt;br /&gt;
This technique uses liquid photopolymer resin, cured layer by layer with ultraviolet light. SLA/DLP printers have the advantages of a very high resolution, smooth surfaces and are ideal for compact and detailed models (e.g., small proteins rendered as surface, ligands, or symmetric assemblies). This technology has its own limitations, such as higher material cost, post-processing requirements (washing and UV-curing), and the need for careful handling of resin.&lt;br /&gt;
&lt;br /&gt;
When choosing between FDM and SLA printers, model size and resolution are the key criteria: &#039;&#039;&#039;FDM&#039;&#039;&#039; is preferred for &#039;&#039;large, educational display models&#039;&#039;; &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; is optimal for &#039;&#039;small, precise structures&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
While FDM and SLA/DLP are the most widely used technologies in educational and research contexts due to their accessibility, other additive manufacturing methods also exist —such as &#039;&#039;Selective Laser Sintering&#039;&#039; (SLS), &#039;&#039;PolyJet&#039;&#039;, and &#039;&#039;Binder Jetting&#039;&#039;— each employing different materials and curing mechanisms. These industrial-grade techniques can produce highly detailed or multi-material parts but are generally more expensive and less accessible for classroom use. For an overview of major 3D-printing technologies, see [https://all3dp.com/1/types-of-3d-printers-3d-printing-technology/ All3DP: Complete Overview of the Types of 3D Printers]&lt;br /&gt;
&lt;br /&gt;
=== Single- vs. Multi-Material Printers ===&lt;br /&gt;
Most entry-level desktop 3D printers use a single filament or resin, producing models in one color or material. However, multi-material systems (such as [https://eu.store.bambulab.com/products/ams-multicolor-printing?from=home_web_top_navigation Bambu Lab AMS] and its variants or [https://www.prusa3d.com/category/original-prusa-mmu3/ Prusa MMU3]) can simultaneously print multiple filaments, enabling color-coded domains, subunits, or ligands directly in one print. For complex color information, users can also apply post-print color coding (painting or labeling) or print separate parts and assemble them manually.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A large FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A multi-material FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Small resin-printed models&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:GABAA_receptor.png|320px|center|thumb| GABAA receptor, [[6x3x]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Bacterial_Ribosome_multimaterial_FDM.png|348px|center|thumb| Bacterial 70S ribosome, [[4v5d]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Dna_insuline_sla.png|252px|center|thumb|DNA (left) and insulin (right) models, [[4bna]] and [[4ins]], scale at the bottom in cm]]&lt;br /&gt;
|-&lt;br /&gt;
|Trace Model of the GABAA receptor printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com] &lt;br /&gt;
|Surface model of the Bacterial 70S ribosome printed on a multi-material capable printer (BambuLab X1C AMS). Blue and violet are ribosomal proteins, orange and yellow are rRNAs, and black is tRNA. Printable files available on [https://www.printables.com/model/1430877-bacterial-70s-ribosome Printables.com]&lt;br /&gt;
|Balls and sticks and cartoon models of DNA (right) and insulin (left)&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== File Formats Used in 3D Printing ===&lt;br /&gt;
Proteopedia supports two export formats for generating printable molecular models:&lt;br /&gt;
*&#039;&#039;&#039;.STL&#039;&#039;&#039; (Stereolithography): the most common and universally compatible format; encodes only surface geometry, without color or texture information.&lt;br /&gt;
*&#039;&#039;&#039;.OBJ&#039;&#039;&#039; (Wavefront Object) with an associated &#039;&#039;&#039;.MTL&#039;&#039;&#039; (Material Template Library) files: includes both geometry and optional color/texture data; useful for color prints.&lt;br /&gt;
&lt;br /&gt;
Another widely adopted file format used in 3D printing is the &#039;&#039;&#039;.3MF&#039;&#039;&#039; (3D Manufacturing Format): a modern open standard that stores geometry, color, and multi-material metadata in a single file—recommended for advanced printers. For a more extensive pros and cons of different 3D printing file formats please see [https://all3dp.com/2/3d-file-format-3d-model-types/ The Main 3D Printing File Formats on all3dp]. &lt;br /&gt;
&lt;br /&gt;
STL is ideal for single-color models and maximum compatibility, while OBJ/MTL is recommended for multi-material workflows. 3MF files will be used in this tutorial to save the model and printing settings. &lt;br /&gt;
&lt;br /&gt;
Support in Proteopedia for these formats is based on the export capabilities of Jmol/JSmol; for details, see [http://wiki.jmol.org/index.php/File_formats/3D_Objects#STL STL] and [http://wiki.jmol.org/index.php/File_formats/3D_Objects#OBJ OBJ]&lt;br /&gt;
&lt;br /&gt;
== Overview of the 3D printing process ==&lt;br /&gt;
3D printing enables the transformation of atomic-level structural data into tangible macromolecular models that can be explored through both sight and touch.  &lt;br /&gt;
The process generally follows several main steps, each requiring specific types of software and hardware.&lt;br /&gt;
[[Image:3D_printing_workflow_v2.png|thumb|left|400px|Overview of the 3D printing workflow for generating physical molecular models.]]&lt;br /&gt;
	&lt;br /&gt;
=== Preparing the structure and generating a printable File ===&lt;br /&gt;
:The first stage involves creating a printable three-dimensional representation of the molecule. Some molecular-graphics programs such as [https://www.pymol.org/ PyMOL], [https://www.rbvi.ucsf.edu/chimerax/ UCSF ChimeraX], [https://molstar.org/Mol*], or [https://jmol.sourceforge.net/ Jmol] can be used not only to visualize a structure (from the Protein Data Bank or other sources), but also to export the resulting geometry in a .STL or .OBJ format. However, the default visualization styles of these programs are &#039;&#039;&#039;&#039;&#039;not directly suitable for 3D printing&#039;&#039;&#039;&#039;&#039;. Therefore, when preparing a model for fabrication, it is important to:&lt;br /&gt;
:* &#039;&#039;&#039;Select an appropriate molecular representation&#039;&#039;&#039; (e.g., surface, cartoon, sticks, spheres) depending on the pedagogical or structural feature you wish to highlight.  &lt;br /&gt;
:* &#039;&#039;&#039;Add struts or connectors&#039;&#039;&#039; to increase the mechanical stability of the model, especially for large complexes or long helices.  &lt;br /&gt;
:* &#039;&#039;&#039;Remove specific struts or pseudobonds&#039;&#039;&#039; when individual components — ligands, subunits, or cofactors — need to remain detachable.  &lt;br /&gt;
:* &#039;&#039;&#039;Adjust thickness&#039;&#039;&#039; of atoms, bonds, helices, and sheets to ensure adequate rigidity and printability (features thinner than the printer’s nozzle diameter or resin resolution may break).  &lt;br /&gt;
:* &#039;&#039;&#039;Apply meaningful coloring&#039;&#039;&#039; when preparing multi-material prints, for instance, to distinguish domains, chains, ligands or atoms.&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene that automates the process and enables users to effortlessly generate 3D-printable molecular models - more on that in the corresponding section [[#Generating printable files on Proteopedia|Generating printable files on Proteopedia]] within this page. For advanced users wanting to do this manually, we highly recommend two guides: &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot; /&amp;gt; and &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
=== Slicing the Model ===&lt;br /&gt;
Before printing, the STL file must be processed by a &#039;&#039;&#039;slicer&#039;&#039;&#039; — specialized software that converts 3D geometry into a series of horizontal layers. The slicer also generates &#039;&#039;&#039;G-code&#039;&#039;&#039;, the set of instructions that control the printer. These commands are printer-specific and include parameters such as extrusion speed, layer thickness, temperature, and movement. Together, they are usually stored as a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;.  &lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an FDM printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;number of perimeters&#039;&#039;&#039;, which affects mechanical strength and print time;&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines resolution and print duration;&lt;br /&gt;
:* &#039;&#039;&#039;infill density&#039;&#039;&#039;, which determines internal strength and affects print time;&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, temporary structures that hold overhanging regions;&lt;br /&gt;
:* &#039;&#039;&#039;print orientation&#039;&#039;&#039;, which influences surface quality, mechanical strength, and the amount of supports required.&lt;br /&gt;
:All these parameters make up a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. In this step, users must also select the material-specific parameters, or apply a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. More details on these profiles are provided later on this page.&lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines vertical resolution and print time; thinner layers produce smoother surfaces but significantly increase printing duration.&lt;br /&gt;
:* &#039;&#039;&#039;exposure time&#039;&#039;&#039;, which controls how long each layer is cured by UV light; optimal exposure ensures proper adhesion between layers without over-curing fine details.&lt;br /&gt;
:* &#039;&#039;&#039;bottom-layer exposure and count&#039;&#039;&#039;, which influence model adhesion to the build platform — longer exposures and additional base layers improve stability during printing.&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, which anchor the model to the build plate and prevent deformation during peeling; proper placement reduces surface marks and print failures.&lt;br /&gt;
:* &#039;&#039;&#039;model orientation&#039;&#039;&#039;, which affects surface quality, support contact area, and resin drainage; angling the model (typically 30–45°) minimizes suction forces and improves print reliability.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for FDM printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for resin printing&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:Insuline_sliced_prusa.gif|386px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|[[Image:Insuline_Sliced_SLA.gif|372px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|-&lt;br /&gt;
|Cartoon model of insulin sliced in PrusaSlicer and ready to be printed on FDM printers. The arrow shows the trajectory of the print head on a single slice or layer. Orange is the model, green are the supports. &lt;br /&gt;
|Cartoon model of insulin sliced in Elegoo SatelLite and ready to be printed on FDM printer.On the left, with blue is the model, with gray are the supports. On the right is the image on the UV screen. &lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== 3D Printing the Model ===&lt;br /&gt;
:The prepared G-code is then transferred to the 3D printer, either via an SD card, USB flash drive, or Wi-Fi connection. During printing, close observation of the first few layers is essential to ensure good adhesion to the build plate and a successful print. Total printing time depends on model size, selected layer height, and printer speed. &#039;&#039;Small peptide&#039;&#039; models may print in &#039;&#039;&#039;less than an hour&#039;&#039;&#039;, whereas l&#039;&#039;arge multimeric assemblies&#039;&#039; can require &#039;&#039;&#039;several hours or days&#039;&#039;&#039;. &#039;&#039;Multi-color&#039;&#039; or &#039;&#039;multi-material&#039;&#039; prints generally take &#039;&#039;&#039;longer&#039;&#039;&#039;, while &#039;&#039;SLA/DLP&#039;&#039; printers are generally &#039;&#039;&#039;faster&#039;&#039;&#039; due to their simultaneous layer exposure.&lt;br /&gt;
=== Post-Processing ===&lt;br /&gt;
:After printing, the model undergoes post-processing, which varies depending on the printing technology used:&lt;br /&gt;
:* For &#039;&#039;&#039;FDM prints&#039;&#039;&#039;, supports are removed mechanically, and surfaces can be smoothed by light sanding or polishing.&lt;br /&gt;
:* For &#039;&#039;&#039;resin prints&#039;&#039;&#039;, supports are removed mechanically, parts are washed in isopropanol to remove uncured resin and then exposed to UV light for final curing.&lt;br /&gt;
:Models printed in multiple parts can be assembled using cyanoacrylate or epoxy adhesive. Optional finishing steps (painting, labeling) can improve contrast between subunits or highlight functional regions.&lt;br /&gt;
&lt;br /&gt;
==Generating printable files on Proteopedia==&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene, enabling logged users to effortlessly generate 3D-printable molecular models directly from its pages. The tool is powered by [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;], a script that analyzes the structural data and automatically scales the model’s geometry to match the printable volume of a medium-size desktop 3D printer (e.g., Ender-3, 210×210×210 mm). During this process, the tool evaluates the molecular bounding box, atom radii, and bond lengths, then proportionally adjusts all dimensions to achieve a realistic and mechanically robust print scale — preserving scientific accuracy while ensuring manufacturability. For advanced users, [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;] may also be used in conjunction with the [https://jmol.sourceforge.net/ &#039;&#039;&#039;Jmol&#039;&#039;&#039;] program, providing full access to its scripting capabilities and advanced export features.&lt;br /&gt;
==Step-by-step guide for automatic generation of printable files on Proteopedia==&lt;br /&gt;
=== Open a structure and access the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool ===&lt;br /&gt;
Log in with your Proteopedia Username and password. Navigate to any Proteopedia page (for example, [[Introduction_to_protein_structure]]). The corresponding 3D structure will load in the viewer on the right.  &lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_button_in_Proteopedia.png|thumb|left|400px|The &#039;&#039;&#039;Print3D&#039;&#039;&#039; button on a Proteopedia page]]&lt;br /&gt;
&lt;br /&gt;
At the bottom of the structure display window, locate and click the &#039;&#039;&#039;Print3D&#039;&#039;&#039; button. The tool will launch and begin analyzing the current molecular structure.  &lt;br /&gt;
This process may take some time to complete, depending on the size of the structure.  &lt;br /&gt;
Please wait until the message &#039;&#039;&#039;Analyzing structure...&#039;&#039;&#039; disappears and the next page is displayed — this marks the start of the two-step printing workflow.&lt;br /&gt;
=== Select a molecular representation and a printing scale ===&lt;br /&gt;
In this new page, some user input is required. Each option includes a short explanation; the key steps are outlined below, but feel free to explore and adopt the settings that best fit your use case.&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step1.png|thumb|left|400px|Selecting molecular representation and printing scale]]&lt;br /&gt;
&lt;br /&gt;
(1) &#039;&#039;&#039;Choose a molecular representation&#039;&#039;&#039; from the &#039;&#039;&#039;Scheme&#039;&#039;&#039; list, based on your goal:&lt;br /&gt;
* &#039;&#039;&#039;Backbone&#039;&#039;&#039;, &#039;&#039;&#039;Trace&#039;&#039;&#039;, or &#039;&#039;&#039;Ribbon&#039;&#039;&#039; — to emphasize secondary structure (effective for teaching protein folds).&lt;br /&gt;
* &#039;&#039;&#039;Surface&#039;&#039;&#039; — to highlight molecular topology and binding sites.&lt;br /&gt;
* &#039;&#039;&#039;Ball &amp;amp; Stick&#039;&#039;&#039; — atom-level detail for ligands or small molecules; usually impractical for large proteins or complexes.&lt;br /&gt;
* &#039;&#039;&#039;Proteopedia Scene&#039;&#039;&#039; — attempts to render the current page’s scene directly; may not work for all scenes. This is not fully implemented and only available for a few users.&lt;br /&gt;
&#039;&#039;Note:&#039;&#039; Some representations may be unavailable for a given structure because they are not printable in a reliable way.&lt;br /&gt;
&lt;br /&gt;
(2) In the &#039;&#039;&#039;Printer&#039;&#039;&#039; section, select whether you want a &#039;&#039;&#039;single-color&#039;&#039;&#039; or a &#039;&#039;&#039;multi-color&#039;&#039;&#039; print.&lt;br /&gt;
&lt;br /&gt;
(3) In the &#039;&#039;&#039;Printer scale&#039;&#039;&#039; section, set the desired size of the printed model. The tool constrains safe sizes based on the chosen representation and displays the physical dimensions (mm). &#039;&#039;&#039;Important! Please note the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;printer scale value in %&amp;lt;/span&amp;gt; as it is going to be required downstream in the next section of this workflow, [[#Printing files from Proteopedia|Printing files from Proteopedia]]&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
(4) When ready, click the green &#039;&#039;&#039;Make printer files&#039;&#039;&#039; button. Please wait patiently until the  &#039;&#039;Generating files for 3D printing of...&#039;&#039; message disappears and the final step is displayed.&lt;br /&gt;
&lt;br /&gt;
===Download the .STL or .OBJ files===&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step2.png|thumb|left|400px|Final step in generating printable files]]&lt;br /&gt;
&lt;br /&gt;
In this final page, a 3D preview of the generated model is displayed.&lt;br /&gt;
You can use the mouse to rotate, zoom, and inspect the model from different angles. If the result meets your needs, click the green (A) &#039;&#039;&#039;Download files&#039;&#039;&#039; button and save the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive containing the &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; files on your computer. If your model needs further improvements, hit the green (B) &#039;&#039;&#039;Same structure&#039;&#039;&#039; button to return to the previous screen and adjust your settings.&lt;br /&gt;
&lt;br /&gt;
 maybe a movie is better- need to decide ?&lt;br /&gt;
&lt;br /&gt;
{{clear}}&lt;br /&gt;
== Printing files from Proteopedia ==&lt;br /&gt;
Unzipping the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive will produce the exported &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file, along with an optional &#039;&#039;&#039;.MTL&#039;&#039;&#039; material file. &lt;br /&gt;
=== Using 3D printing services ===&lt;br /&gt;
If you do not have a 3D printer, you can still obtain physical models by using locally available 3D-printing services. Just search on [https://www.google.com/maps Google Maps] with the term  &#039;&#039;&#039;3D printing&#039;&#039;&#039; in your area. Here is short list of well-known 3D Printing service providers that may also ship worldwide: &lt;br /&gt;
&lt;br /&gt;
* [https://www.shapeways.com/ &#039;&#039;&#039;Shapeways&#039;&#039;&#039;] — global service offering a wide range of materials and colors. Educational discounts are available through their academic program.&lt;br /&gt;
* [https://www.sculpteo.com/en/ &#039;&#039;&#039;Sculpteo&#039;&#039;&#039;] — Europe-based provider offering fast turnaround and many printing technologies, including resin and polymer options.&lt;br /&gt;
* [https://www.xometry.com/capabilities/3d-printing-service &#039;&#039;&#039;Xometry&#039;&#039;&#039;] — large international network providing access to industrial-grade printing methods such as FDM, SLA, SLS, and DMLS.&lt;br /&gt;
* [https://craftcloud3d.com/ &#039;&#039;&#039;Craftcloud&#039;&#039;&#039;] — an aggregator that compares multiple providers and finds the best price and lead time for your uploaded model.&lt;br /&gt;
&lt;br /&gt;
When contacting a printing service, provide the exported files together with the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value in %&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ([[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). It is also advisable to share the link to this Proteopedia page so that the operator understands the peculiarities of printing molecular models. &lt;br /&gt;
&lt;br /&gt;
=== Using a desktop 3D printer ===&lt;br /&gt;
&lt;br /&gt;
Before importing the .STL or .OBJ file into your slicer software, it is recommended to inspect and, if necessary, repair the model to ensure printability. Common issues include non-manifold geometry, intersecting faces, and missing surfaces.  The example below demonstrates how to use [https://www.blender.org/ &#039;&#039;&#039;Blender&#039;&#039;&#039;] together with its [https://extensions.blender.org/add-ons/print3d-toolbox/ &#039;&#039;&#039;3D Print Toolbox extension&#039;&#039;&#039;] to improve the printability of the .STL and .OBJ files generated with the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in [[Proteopedia]]. &#039;&#039;&#039;Important note&#039;&#039;&#039;: The repair process is largely automated but may introduce artifacts. Carefully inspect the corrected model for any missing or distorted sections, atoms, or bonds, and determine whether these omissions affect the intended purpose of the printed model.  &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for single color or resin printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for multi-color FDM printing&lt;br /&gt;
|-&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=k6u-5JnoP-c&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=OCisrIZMIDM&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|}  &lt;br /&gt;
&lt;br /&gt;
Once the repaired &#039;&#039;&#039;.STL or .OBJ&#039;&#039;&#039; file is ready, it can be imported into your slicer software. In this step, you will prepare the file for printing by applying appropriate printer, filament, and print-settings profiles.&lt;br /&gt;
&lt;br /&gt;
*Apply the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value (%)&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ( [[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). This step ensures that the model fits your print bed and maintains structural integrity during printing. The location of the scale (%) input field varies depending on the slicer software you are using.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Orient the model on the print bed&#039;&#039;&#039; so that its largest, flattest surface rests on the bed. This minimizes the need for supports and improves adhesion. If your slicer includes an Auto Orient or Auto Arrange function, use it to optimize placement. (&#039;&#039;Hint&#039;&#039;: Bambu Studio and Orca Slicer include this feature, Ultimaker Cura has a [https://marketplace.ultimaker.com/app/cura/plugins/nallath/OrientationPlugin Auto-Orientation plugin] available, while PrusaSlicer currently does not.)&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Select the printer&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that matches your device.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Choose the material&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; corresponding to the filament type (e.g., PLA, PETG, TPU) and manufacturer you intend to use.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Adjust the printing parameters&#039;&#039;&#039; by selecting a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that defines layer height, infill, speed, and support options.&lt;br /&gt;
&lt;br /&gt;
In most cases, the default &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; and &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; provided by the slicer are sufficient. However, molecular models often include overhangs, thin connections, and complex internal geometries, which require additional supports and reinforced perimeters to ensure structural stability. For this reason, the default &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; may not yield optimal results.&lt;br /&gt;
&lt;br /&gt;
Validated printing profiles for the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool are available for several printer models. These profiles provide optimized settings that produce sturdy models, reduce material consumption, and shorten print time, ensuring consistent and reliable results. Three distinct profiles are supplied, corresponding to major molecular representations: &#039;&#039;&#039;balls and sticks&#039;&#039;&#039;, &#039;&#039;&#039;surface&#039;&#039;&#039;, and &#039;&#039;&#039;cartoon&#039;&#039;&#039;. The &#039;&#039;&#039;cartoon&#039;&#039;&#039; profile is also suitable for &#039;&#039;&#039;backbone&#039;&#039;&#039;, &#039;&#039;&#039;trace&#039;&#039;&#039;, and &#039;&#039;&#039;ribbon&#039;&#039;&#039; representations. For some printers, each profile is supplied in two variants, one using standard supports and one using tree or organic supports. In the case of multi-material printers, profiles for printing with soluble support and soluble interface are also provided.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer brand and model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Profiles provided as / Slicer&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer Type, nozle size and multi-material support&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |GitHub with profiles&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to import profiles into Slicer&lt;br /&gt;
|-&lt;br /&gt;
|Original Prusa Core One&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer ]&lt;br /&gt;
|FDM / 0.4 mm / yes, 5 colors, if MMU3 installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/Prusa%20CoreOne CoreOne]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab A1Mini&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, 4 colors if AMS Lite is installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/BambuLab%20A1Mini AiMini]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab X1 Carbon&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, up to 16 colors if multiple AMS are installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ca92e7de9c72505c1b9b09e912ad177341cabc9a/BambuLab%20X1C X1Carbon]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|- &lt;br /&gt;
|Original Prusa MK3S+&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/7a7ee68d1e19f063600f53def49a99dfefbc595d/Prusa%20MK3S%2B MK3S+]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 5 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/a653c7cc6b3dec86b90117cc450d1883cc4a80bd/Ender-5-Pro Ender5Pro]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 3 v2 with a ENDERIDEX kit&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / yes, IDEX, two filaments&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/c2c74f1261a42c160e7e3898a407f21465de2ca7/Ender3-IDEX Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Kingroon KPS3 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ea733b2d05020b99f91c92f71a039c5ba8e54108/Kingroon-KPS3-Pro Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Elegoo Mars 5 Ultra&lt;br /&gt;
|no profile needed, just be sure to add supports / [https://www.elegoo.com/pages/satellite-3d-slicer?srsltid=AfmBOopMQGHgHycHMFOZALzOIC8z7bVlSHjL_jj2ShYR4QkowYKmKzUx ELEGOO SatelLite]&lt;br /&gt;
|resin / - / no&lt;br /&gt;
|&lt;br /&gt;
|no profile needed, default settings worked, just be sure to add supports. EVO supports worked well enough.  Post-processing steps: 1)washing: at least 10 min. 2) support removal 3)curring: at least 10 min on a Elegoo Mercury Plus V3.0&lt;br /&gt;
|- &lt;br /&gt;
|} &lt;br /&gt;
&#039;&#039;&#039;Notes&#039;&#039;&#039;: &lt;br /&gt;
* These profiles were developed and validated with the support of EDUMOL3D, Project [http://cercetare.bio.uaic.ro/grupuri/bioactive/content/grants/PED2024_mm.html PN-IV-P7-7.1-PED-2024-0343] financed by the Ministry of Research, Innovation and Digitization, [https://uefiscdi.gov.ro/ UEFISCDI], Romania.&lt;br /&gt;
* The profiles are a work in progress. Please check GitHub for updates. If you have suggestions for improvements, please drop a message at marius.mihasan(@)uaic.ro&lt;br /&gt;
&lt;br /&gt;
==== &#039;&#039;&#039;Note on multi-color printing &#039;&#039;&#039; ====&lt;br /&gt;
To our knowledge, only &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039; and &#039;&#039;&#039;Orca Slicer&#039;&#039;&#039; can automatically import color information from the &#039;&#039;&#039;.MTL&#039;&#039;&#039; file associated with the printable &#039;&#039;&#039;.OBJ&#039;&#039;&#039; generated by the Proteopedia &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool.  &lt;br /&gt;
At present, &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; does not support importing &#039;&#039;&#039;.MTL&#039;&#039;&#039; files directly.&lt;br /&gt;
&lt;br /&gt;
A practical workaround for &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; users is as follows:  &lt;br /&gt;
# Open the &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file in &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039;.  &lt;br /&gt;
#Verify or adjust the color mapping as needed.  &lt;br /&gt;
#Export the model as a generic &#039;&#039;&#039;.3MF&#039;&#039;&#039; file using the menu command:  &#039;&#039;File&#039;&#039; → &#039;&#039;Export&#039;&#039; → &#039;&#039;Export Generic 3MF...&#039;&#039;  &lt;br /&gt;
#Open the exported &#039;&#039;&#039;.3MF&#039;&#039;&#039; file in &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;. The color data will now be available under the &#039;&#039;&#039;Multimaterial Painting&#039;&#039;&#039; tool.&lt;br /&gt;
&lt;br /&gt;
This workflow preserves the original coloring assigned in Proteopedia and allows successful multi-color or multi-material printing on any capable 3D printer compatible with &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Other relevant resources ==&lt;br /&gt;
[[Print3D_models_gallery]] - examples of 3D printed molecular models from Proteopedia users.&lt;br /&gt;
&lt;br /&gt;
[https://3d.nih.gov/ NIH 3D Print Exchange] - an open, community-driven portal to download, share, and create bioscientific and medical 3D models, including for 3D printing.&lt;br /&gt;
  &lt;br /&gt;
[https://github.com/mariusmihasan/3DP-Jmol 3DP-Jmol] - the Jmol/JSmol behind the Print3D tool. Automatically generates 3D printable molecular models from structural data and can be easily integrated into web pages.&lt;br /&gt;
&lt;br /&gt;
[https://pdb101.rcsb.org/learn/3d-printing/pdb-structures-and-3d-printing 3D Printing on PDB101] - a quick guide on 3D printing molecular models and a small curated 3D models for education&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;If you print a model from Proteopedia, please share photos and feedback — let’s 3D print the whole Proteopedia!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386105</id>
		<title>Print3D help</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386105"/>
		<updated>2025-10-27T10:04:09Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== Proteopedia and 3D Printing ==&lt;br /&gt;
&lt;br /&gt;
Physical molecular models, by engaging both visual and tactile senses, provide an effective means of deepening the understanding of complex concepts in molecular biology and biochemistry. They allow students to perceive the three-dimensional organization of macromolecules, thereby enhancing comprehension of the relationship between structure and function &amp;lt;ref&amp;gt;PMID: 32590880&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 40214166&amp;lt;/ref&amp;gt;. Numerous studies have demonstrated that the use of tangible models in science education improves learning outcomes, fosters conceptual reasoning, and increases student engagement &amp;lt;ref&amp;gt;PMID: 27366318&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 26712513&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;Larsson, C., Tibell, L.A.E. Challenging Students’ Intuitions—the Influence of a Tangible Model of Virus Assembly on Students’ Conceptual Reasoning About the Process of Self-Assembly. Res Sci Educ 45, 663–690 (2015). [http://dx.doi.org/10.1007/s11165-014-9446-6 DOI: 110.1007/s11165-014-9446-6]&amp;lt;/ref&amp;gt;. The rapid development of 3D-printing technologies has made it possible to create customized and affordable molecular models  &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot;&amp;gt;PMID: 28362403&amp;lt;/ref&amp;gt; &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot;&amp;gt;PMID: 33755300&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 33384761&amp;lt;/ref&amp;gt;. &lt;br /&gt;
&lt;br /&gt;
Affordable desktop 3D printers can now be used to fabricate physical models from virtually any structure or scene on [[Proteopedia]]. This page provides an introduction to 3D printing, a step-by-step guide to generating printable files directly from [[Proteopedia]], and several tested printing profiles for common printers (e.g., Prusa Research, Bambu Lab, Creality, or Elegoo).&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== «3D Printing 101»: an introduction to 3D printing ==&lt;br /&gt;
3D printing, also known as &#039;&#039;additive manufacturing&#039;&#039;, builds physical objects layer by layer from digital designs. For more technical details please head for the excellent introductory article on [https://all3dp.com/2/what-is-3d-printing/ All3DP].  In structural biology education, 3D printing provides an affordable and accessible way to transform atomic coordinate data (e.g., from PDB, MOL or SDF files) into tangible molecular models that can be observed, handled, and discussed in class or laboratory settings.&lt;br /&gt;
&lt;br /&gt;
=== Printer Types: FDM vs. SLA/DLP ===&lt;br /&gt;
The two most accessible 3D-printing technologies that can be used to create molecular models are:&lt;br /&gt;
* &#039;&#039;&#039;FDM (Fused Deposition Modeling)&#039;&#039;&#039;&lt;br /&gt;
This method extrudes a heated thermoplastic filament (such as PLA, PETG or TPU) through a fine nozzle, depositing successive layers that form the model. FDM printers have the advantages of low cost, easy maintenance, wide availability, and being capable of printing large and colorful molecular models. This technology has a few limitations, such as: visible layer lines, lower surface resolution, and less suited for very small or intricate molecular details.&lt;br /&gt;
* &#039;&#039;&#039;SLA/DLP (Resin Printing)&#039;&#039;&#039;&lt;br /&gt;
This technique uses liquid photopolymer resin, cured layer by layer with ultraviolet light. SLA/DLP printers have the advantages of a very high resolution, smooth surfaces and are ideal for compact and detailed models (e.g., small proteins rendered as surface, ligands, or symmetric assemblies). This technology has its own limitations, such as higher material cost, post-processing requirements (washing and UV-curing), and the need for careful handling of resin.&lt;br /&gt;
&lt;br /&gt;
When choosing between FDM and SLA printers, model size and resolution are the key criteria: &#039;&#039;&#039;FDM&#039;&#039;&#039; is preferred for &#039;&#039;large, educational display models&#039;&#039;; &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; is optimal for &#039;&#039;small, precise structures&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
While FDM and SLA/DLP are the most widely used technologies in educational and research contexts due to their accessibility, other additive manufacturing methods also exist —such as &#039;&#039;Selective Laser Sintering&#039;&#039; (SLS), &#039;&#039;PolyJet&#039;&#039;, and &#039;&#039;Binder Jetting&#039;&#039;— each employing different materials and curing mechanisms. These industrial-grade techniques can produce highly detailed or multi-material parts but are generally more expensive and less accessible for classroom use. For an overview of major 3D-printing technologies, see [https://all3dp.com/1/types-of-3d-printers-3d-printing-technology/ All3DP: Complete Overview of the Types of 3D Printers]&lt;br /&gt;
&lt;br /&gt;
=== Single- vs. Multi-Material Printers ===&lt;br /&gt;
Most entry-level desktop 3D printers use a single filament or resin, producing models in one color or material. However, multi-material systems (such as [https://eu.store.bambulab.com/products/ams-multicolor-printing?from=home_web_top_navigation Bambu Lab AMS] and its variants or [https://www.prusa3d.com/category/original-prusa-mmu3/ Prusa MMU3]) can simultaneously print multiple filaments, enabling color-coded domains, subunits, or ligands directly in one print. For complex color information, users can also apply post-print color coding (painting or labeling) or print separate parts and assemble them manually.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A large FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A multi-material FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Small resin-printed models&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:GABAA_receptor.png|320px|center|thumb| GABAA receptor, [[6x3x]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Bacterial_Ribosome_multimaterial_FDM.png|348px|center|thumb| Bacterial 70S ribosome, [[4v5d]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Dna_insuline_sla.png|252px|center|thumb|DNA (left) and insulin (right) models, [[4bna]] and [[4ins]], scale at the bottom in cm]]&lt;br /&gt;
|-&lt;br /&gt;
|Trace Model of the GABAA receptor printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com] &lt;br /&gt;
|Surface model of the Bacterial 70S ribosome printed on a multi-material capable printer (BambuLab X1C AMS). Blue and violet are ribosomal proteins, orange and yellow are rRNAs, and black is tRNA. Printable files available on [https://www.printables.com/model/1430877-bacterial-70s-ribosome Printables.com]&lt;br /&gt;
|Balls and sticks and cartoon models of DNA (right) and insulin (left)&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== File Formats Used in 3D Printing ===&lt;br /&gt;
Proteopedia supports two export formats for generating printable molecular models:&lt;br /&gt;
*&#039;&#039;&#039;.STL&#039;&#039;&#039; (Stereolithography): the most common and universally compatible format; encodes only surface geometry, without color or texture information.&lt;br /&gt;
*&#039;&#039;&#039;.OBJ&#039;&#039;&#039; (Wavefront Object) with an associated &#039;&#039;&#039;.MTL&#039;&#039;&#039; (Material Template Library) files: includes both geometry and optional color/texture data; useful for color prints.&lt;br /&gt;
&lt;br /&gt;
Another widely adopted file format used in 3D printing is the &#039;&#039;&#039;.3MF&#039;&#039;&#039; (3D Manufacturing Format): a modern open standard that stores geometry, color, and multi-material metadata in a single file—recommended for advanced printers. For a more extensive pros and cons of different 3D printing file formats please see [https://all3dp.com/2/3d-file-format-3d-model-types/ The Main 3D Printing File Formats on all3dp]. &lt;br /&gt;
&lt;br /&gt;
STL is ideal for single-color models and maximum compatibility, while OBJ/MTL is recommended for multi-material workflows. 3MF files will be used in this tutorial to save the model and printing settings. &lt;br /&gt;
&lt;br /&gt;
Support in Proteopedia for these formats is based on the export capabilities of Jmol/JSmol; for details, see [http://wiki.jmol.org/index.php/File_formats/3D_Objects#STL STL] and [http://wiki.jmol.org/index.php/File_formats/3D_Objects#OBJ OBJ]&lt;br /&gt;
&lt;br /&gt;
== Overview of the 3D printing process ==&lt;br /&gt;
3D printing enables the transformation of atomic-level structural data into tangible macromolecular models that can be explored through both sight and touch.  &lt;br /&gt;
The process generally follows several main steps, each requiring specific types of software and hardware.&lt;br /&gt;
[[Image:3D_printing_workflow_v2.png|thumb|left|400px|Overview of the 3D printing workflow for generating physical molecular models.]]&lt;br /&gt;
	&lt;br /&gt;
=== Preparing the structure and generating a printable File ===&lt;br /&gt;
:The first stage involves creating a printable three-dimensional representation of the molecule. Some molecular-graphics programs such as [https://www.pymol.org/ PyMOL], [https://www.rbvi.ucsf.edu/chimerax/ UCSF ChimeraX], [https://molstar.org/Mol*], or [https://jmol.sourceforge.net/ Jmol] can be used not only to visualize a structure (from the Protein Data Bank or other sources), but also to export the resulting geometry in a .STL or .OBJ format. However, the default visualization styles of these programs are &#039;&#039;&#039;&#039;&#039;not directly suitable for 3D printing&#039;&#039;&#039;&#039;&#039;. Therefore, when preparing a model for fabrication, it is important to:&lt;br /&gt;
:* &#039;&#039;&#039;Select an appropriate molecular representation&#039;&#039;&#039; (e.g., surface, cartoon, sticks, spheres) depending on the pedagogical or structural feature you wish to highlight.  &lt;br /&gt;
:* &#039;&#039;&#039;Add struts or connectors&#039;&#039;&#039; to increase the mechanical stability of the model, especially for large complexes or long helices.  &lt;br /&gt;
:* &#039;&#039;&#039;Remove specific struts or pseudobonds&#039;&#039;&#039; when individual components — ligands, subunits, or cofactors — need to remain detachable.  &lt;br /&gt;
:* &#039;&#039;&#039;Adjust thickness&#039;&#039;&#039; of atoms, bonds, helices, and sheets to ensure adequate rigidity and printability (features thinner than the printer’s nozzle diameter or resin resolution may break).  &lt;br /&gt;
:* &#039;&#039;&#039;Apply meaningful coloring&#039;&#039;&#039; when preparing multi-material prints, for instance, to distinguish domains, chains, ligands or atoms.&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene that automates the process and enables users to effortlessly generate 3D-printable molecular models - more on that in the corresponding section [[#Generating printable files on Proteopedia|Generating printable files on Proteopedia]] within this page. For advanced users wanting to do this manually, we highly recommend two guides: &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot; /&amp;gt; and &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
=== Slicing the Model ===&lt;br /&gt;
Before printing, the STL file must be processed by a &#039;&#039;&#039;slicer&#039;&#039;&#039; — specialized software that converts 3D geometry into a series of horizontal layers. The slicer also generates &#039;&#039;&#039;G-code&#039;&#039;&#039;, the set of instructions that control the printer. These commands are printer-specific and include parameters such as extrusion speed, layer thickness, temperature, and movement. Together, they are usually stored as a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;.  &lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an FDM printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;number of perimeters&#039;&#039;&#039;, which affects mechanical strength and print time;&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines resolution and print duration;&lt;br /&gt;
:* &#039;&#039;&#039;infill density&#039;&#039;&#039;, which determines internal strength and affects print time;&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, temporary structures that hold overhanging regions;&lt;br /&gt;
:* &#039;&#039;&#039;print orientation&#039;&#039;&#039;, which influences surface quality, mechanical strength, and the amount of supports required.&lt;br /&gt;
:All these parameters make up a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. In this step, users must also select the material-specific parameters, or apply a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. More details on these profiles are provided later on this page.&lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines vertical resolution and print time; thinner layers produce smoother surfaces but significantly increase printing duration.&lt;br /&gt;
:* &#039;&#039;&#039;exposure time&#039;&#039;&#039;, which controls how long each layer is cured by UV light; optimal exposure ensures proper adhesion between layers without over-curing fine details.&lt;br /&gt;
:* &#039;&#039;&#039;bottom-layer exposure and count&#039;&#039;&#039;, which influence model adhesion to the build platform — longer exposures and additional base layers improve stability during printing.&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, which anchor the model to the build plate and prevent deformation during peeling; proper placement reduces surface marks and print failures.&lt;br /&gt;
:* &#039;&#039;&#039;model orientation&#039;&#039;&#039;, which affects surface quality, support contact area, and resin drainage; angling the model (typically 30–45°) minimizes suction forces and improves print reliability.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for FDM printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for resin printing&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:Insuline_sliced_prusa.gif|386px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|[[Image:Insuline_Sliced_SLA.gif|372px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|-&lt;br /&gt;
|Cartoon model of insulin sliced in PrusaSlicer and ready to be printed on FDM printers. The arrow shows the trajectory of the print head on a single slice or layer. Orange is the model, green are the supports. &lt;br /&gt;
|Cartoon model of insulin sliced in Elegoo SatelLite and ready to be printed on FDM printer.On the left, with blue is the model, with gray are the supports. On the right is the image on the UV screen. &lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== 3D Printing the Model ===&lt;br /&gt;
:The prepared G-code is then transferred to the 3D printer, either via an SD card, USB flash drive, or Wi-Fi connection. During printing, close observation of the first few layers is essential to ensure good adhesion to the build plate and a successful print. Total printing time depends on model size, selected layer height, and printer speed. &#039;&#039;Small peptide&#039;&#039; models may print in &#039;&#039;&#039;less than an hour&#039;&#039;&#039;, whereas l&#039;&#039;arge multimeric assemblies&#039;&#039; can require &#039;&#039;&#039;several hours or days&#039;&#039;&#039;. &#039;&#039;Multi-color&#039;&#039; or &#039;&#039;multi-material&#039;&#039; prints generally take &#039;&#039;&#039;longer&#039;&#039;&#039;, while &#039;&#039;SLA/DLP&#039;&#039; printers are generally &#039;&#039;&#039;faster&#039;&#039;&#039; due to their simultaneous layer exposure.&lt;br /&gt;
=== Post-Processing ===&lt;br /&gt;
:After printing, the model undergoes post-processing, which varies depending on the printing technology used:&lt;br /&gt;
:* For &#039;&#039;&#039;FDM prints&#039;&#039;&#039;, supports are removed mechanically, and surfaces can be smoothed by light sanding or polishing.&lt;br /&gt;
:* For &#039;&#039;&#039;resin prints&#039;&#039;&#039;, supports are removed mechanically, parts are washed in isopropanol to remove uncured resin and then exposed to UV light for final curing.&lt;br /&gt;
:Models printed in multiple parts can be assembled using cyanoacrylate or epoxy adhesive. Optional finishing steps (painting, labeling) can improve contrast between subunits or highlight functional regions.&lt;br /&gt;
&lt;br /&gt;
==Generating printable files on Proteopedia==&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene, enabling logged users to effortlessly generate 3D-printable molecular models directly from its pages. The tool is powered by [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;], a script that analyzes the structural data and automatically scales the model’s geometry to match the printable volume of a medium-size desktop 3D printer (e.g., Ender-3, 210×210×210 mm). During this process, the tool evaluates the molecular bounding box, atom radii, and bond lengths, then proportionally adjusts all dimensions to achieve a realistic and mechanically robust print scale — preserving scientific accuracy while ensuring manufacturability. For advanced users, [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;] may also be used in conjunction with the [https://jmol.sourceforge.net/ &#039;&#039;&#039;Jmol&#039;&#039;&#039;] program, providing full access to its scripting capabilities and advanced export features.&lt;br /&gt;
==Step-by-step guide for automatic generation of printable files on Proteopedia==&lt;br /&gt;
=== Open a structure and access the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool ===&lt;br /&gt;
Log in with your Proteopedia Username and password. Navigate to any Proteopedia page (for example, [[Introduction_to_protein_structure]]). The corresponding 3D structure will load in the viewer on the right.  &lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_button_in_Proteopedia.png|thumb|left|400px|The &#039;&#039;&#039;Print3D&#039;&#039;&#039; button on a Proteopedia page]]&lt;br /&gt;
&lt;br /&gt;
At the bottom of the structure display window, locate and click the &#039;&#039;&#039;Print3D&#039;&#039;&#039; button. The tool will launch and begin analyzing the current molecular structure.  &lt;br /&gt;
This process may take some time to complete, depending on the size of the structure.  &lt;br /&gt;
Please wait until the message &#039;&#039;&#039;Analyzing structure...&#039;&#039;&#039; disappears and the next page is displayed — this marks the start of the two-step printing workflow.&lt;br /&gt;
=== Select a molecular representation and a printing scale ===&lt;br /&gt;
In this new page, some user input is required. Each option includes a short explanation; the key steps are outlined below, but feel free to explore and adopt the settings that best fit your use case.&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step1.png|thumb|left|400px|Selecting molecular representation and printing scale]]&lt;br /&gt;
&lt;br /&gt;
(1) &#039;&#039;&#039;Choose a molecular representation&#039;&#039;&#039; from the &#039;&#039;&#039;Scheme&#039;&#039;&#039; list, based on your goal:&lt;br /&gt;
* &#039;&#039;&#039;Backbone&#039;&#039;&#039;, &#039;&#039;&#039;Trace&#039;&#039;&#039;, or &#039;&#039;&#039;Ribbon&#039;&#039;&#039; — to emphasize secondary structure (effective for teaching protein folds).&lt;br /&gt;
* &#039;&#039;&#039;Surface&#039;&#039;&#039; — to highlight molecular topology and binding sites.&lt;br /&gt;
* &#039;&#039;&#039;Ball &amp;amp; Stick&#039;&#039;&#039; — atom-level detail for ligands or small molecules; usually impractical for large proteins or complexes.&lt;br /&gt;
* &#039;&#039;&#039;Proteopedia Scene&#039;&#039;&#039; — attempts to render the current page’s scene directly; may not work for all scenes. This is not fully implemented and only available for a few users.&lt;br /&gt;
&#039;&#039;Note:&#039;&#039; Some representations may be unavailable for a given structure because they are not printable in a reliable way.&lt;br /&gt;
&lt;br /&gt;
(2) In the &#039;&#039;&#039;Printer&#039;&#039;&#039; section, select whether you want a &#039;&#039;&#039;single-color&#039;&#039;&#039; or a &#039;&#039;&#039;multi-color&#039;&#039;&#039; print.&lt;br /&gt;
&lt;br /&gt;
(3) In the &#039;&#039;&#039;Printer scale&#039;&#039;&#039; section, set the desired size of the printed model. The tool constrains safe sizes based on the chosen representation and displays the physical dimensions (mm). &#039;&#039;&#039;Important! Please note the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;printer scale value in %&amp;lt;/span&amp;gt; as it is going to be required downstream in the next section of this workflow, [[#Printing files from Proteopedia|Printing files from Proteopedia]]&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
(4) When ready, click the green &#039;&#039;&#039;Make printer files&#039;&#039;&#039; button. Please wait patiently until the  &#039;&#039;Generating files for 3D printing of...&#039;&#039; message disappears and the final step is displayed.&lt;br /&gt;
&lt;br /&gt;
===Download the .STL or .OBJ files===&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step2.png|thumb|left|400px|Final step in generating printable files]]&lt;br /&gt;
&lt;br /&gt;
In this final page, a 3D preview of the generated model is displayed.&lt;br /&gt;
You can use the mouse to rotate, zoom, and inspect the model from different angles. If the result meets your needs, click the green (A) &#039;&#039;&#039;Download files&#039;&#039;&#039; button and save the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive containing the &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; files on your computer. If your model needs further improvements, hit the green (B) &#039;&#039;&#039;Same structure&#039;&#039;&#039; button to return to the previous screen and adjust your settings.&lt;br /&gt;
&lt;br /&gt;
 maybe a movie is better- need to decide ?&lt;br /&gt;
&lt;br /&gt;
{{clear}}&lt;br /&gt;
== Printing files from Proteopedia ==&lt;br /&gt;
Unzipping the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive will produce the exported &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file, along with an optional &#039;&#039;&#039;.MTL&#039;&#039;&#039; material file. &lt;br /&gt;
=== Using 3D printing services ===&lt;br /&gt;
If you do not have a 3D printer, you can still obtain physical models by using locally available 3D-printing services. Just search on [https://www.google.com/maps Google Maps] with the term  &#039;&#039;&#039;3D printing&#039;&#039;&#039; in your area. Here is short list of well-known 3D Printing service providers that may also ship worldwide: &lt;br /&gt;
&lt;br /&gt;
* [https://www.shapeways.com/ &#039;&#039;&#039;Shapeways&#039;&#039;&#039;] — global service offering a wide range of materials and colors. Educational discounts are available through their academic program.&lt;br /&gt;
* [https://www.sculpteo.com/en/ &#039;&#039;&#039;Sculpteo&#039;&#039;&#039;] — Europe-based provider offering fast turnaround and many printing technologies, including resin and polymer options.&lt;br /&gt;
* [https://www.xometry.com/capabilities/3d-printing-service &#039;&#039;&#039;Xometry&#039;&#039;&#039;] — large international network providing access to industrial-grade printing methods such as FDM, SLA, SLS, and DMLS.&lt;br /&gt;
* [https://craftcloud3d.com/ &#039;&#039;&#039;Craftcloud&#039;&#039;&#039;] — an aggregator that compares multiple providers and finds the best price and lead time for your uploaded model.&lt;br /&gt;
&lt;br /&gt;
When contacting a printing service, provide the exported files together with the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value in %&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ([[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). It is also advisable to share the link to this Proteopedia page so that the operator understands the peculiarities of printing molecular models. &lt;br /&gt;
&lt;br /&gt;
=== Using a desktop 3D printer ===&lt;br /&gt;
&lt;br /&gt;
Before importing the .STL or .OBJ file into your slicer software, it is recommended to inspect and, if necessary, repair the model to ensure printability. Common issues include non-manifold geometry, intersecting faces, and missing surfaces.  The example below demonstrates how to use [https://www.blender.org/ &#039;&#039;&#039;Blender&#039;&#039;&#039;] together with its [https://extensions.blender.org/add-ons/print3d-toolbox/ &#039;&#039;&#039;3D Print Toolbox extension&#039;&#039;&#039;] to improve the printability of the .STL and .OBJ files generated with the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in [[Proteopedia]]. &#039;&#039;&#039;Important note&#039;&#039;&#039;: The repair process is largely automated but may introduce artifacts. Carefully inspect the corrected model for any missing or distorted sections, atoms, or bonds, and determine whether these omissions affect the intended purpose of the printed model.  &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for single color or resin printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for multi-color FDM printing&lt;br /&gt;
|-&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=k6u-5JnoP-c&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=OCisrIZMIDM&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|}  &lt;br /&gt;
&lt;br /&gt;
Once the repaired &#039;&#039;&#039;.STL or .OBJ&#039;&#039;&#039; file is ready, it can be imported into your slicer software. In this step, you will prepare the file for printing by applying appropriate printer, filament, and print-settings profiles.&lt;br /&gt;
&lt;br /&gt;
*Apply the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value (%)&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ( [[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). This step ensures that the model fits your print bed and maintains structural integrity during printing. The location of the scale (%) input field varies depending on the slicer software you are using.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Orient the model on the print bed&#039;&#039;&#039; so that its largest, flattest surface rests on the bed. This minimizes the need for supports and improves adhesion. If your slicer includes an Auto Orient or Auto Arrange function, use it to optimize placement. (&#039;&#039;Hint&#039;&#039;: Bambu Studio and Orca Slicer include this feature, Ultimaker Cura has a [https://marketplace.ultimaker.com/app/cura/plugins/nallath/OrientationPlugin Auto-Orientation plugin] available, while PrusaSlicer currently does not.)&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Select the printer&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that matches your device.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Choose the material&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; corresponding to the filament type (e.g., PLA, PETG, TPU) and manufacturer you intend to use.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Adjust the printing parameters&#039;&#039;&#039; by selecting a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that defines layer height, infill, speed, and support options.&lt;br /&gt;
&lt;br /&gt;
In most cases, the default &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; and &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; provided by the slicer are sufficient. However, molecular models often include overhangs, thin connections, and complex internal geometries, which require additional supports and reinforced perimeters to ensure structural stability. For this reason, the default &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; may not yield optimal results.&lt;br /&gt;
&lt;br /&gt;
Validated printing profiles for the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool are available for several printer models. These profiles provide optimized settings that produce sturdy models, reduce material consumption, and shorten print time, ensuring consistent and reliable results. Three distinct profiles are supplied, corresponding to major molecular representations: &#039;&#039;&#039;balls and sticks&#039;&#039;&#039;, &#039;&#039;&#039;surface&#039;&#039;&#039;, and &#039;&#039;&#039;cartoon&#039;&#039;&#039;. The &#039;&#039;&#039;cartoon&#039;&#039;&#039; profile is also suitable for &#039;&#039;&#039;backbone&#039;&#039;&#039;, &#039;&#039;&#039;trace&#039;&#039;&#039;, and &#039;&#039;&#039;ribbon&#039;&#039;&#039; representations. For some printers, each profile is supplied in two variants, one using standard supports and one using tree or organic supports. In the case of multi-material printers, profiles for printing with soluble support and soluble interface are also provided.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer brand and model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Profiles provided as / Slicer&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer Type, nozle size and multi-material support&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |GitHub with profiles&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to import profiles into Slicer&lt;br /&gt;
|-&lt;br /&gt;
|Original Prusa Core One&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer ]&lt;br /&gt;
|FDM / 0.4 mm / yes, 5 colors, if MMU3 installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/Prusa%20CoreOne CoreOne]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab A1Mini&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, 4 colors if AMS Lite is installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/BambuLab%20A1Mini AiMini]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab X1 Carbon&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, up to 16 colors if multiple AMS are installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ca92e7de9c72505c1b9b09e912ad177341cabc9a/BambuLab%20X1C X1Carbon]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|- &lt;br /&gt;
|Original Prusa MK3S+&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/7a7ee68d1e19f063600f53def49a99dfefbc595d/Prusa%20MK3S%2B MK3S+]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 5 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/a653c7cc6b3dec86b90117cc450d1883cc4a80bd/Ender-5-Pro Ender5Pro]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 3 v2 with a ENDERIDEX kit&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / yes, IDEX, two filaments&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/c2c74f1261a42c160e7e3898a407f21465de2ca7/Ender3-IDEX Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Kingroon KPS3 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ea733b2d05020b99f91c92f71a039c5ba8e54108/Kingroon-KPS3-Pro Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Elegoo Mars 5 Ultra&lt;br /&gt;
|no profile needed, just be sure to add supports / [https://www.elegoo.com/pages/satellite-3d-slicer?srsltid=AfmBOopMQGHgHycHMFOZALzOIC8z7bVlSHjL_jj2ShYR4QkowYKmKzUx ELEGOO SatelLite]&lt;br /&gt;
|resin / - / no&lt;br /&gt;
|&lt;br /&gt;
|no profile needed, default settings worked, just be sure to add supports. EVO supports worked well enough.  Post-processing steps: 1)washing: at least 10 min. 2) support removal 3)curring: at least 10 min on a Elegoo Mercury Plus V3.0&lt;br /&gt;
|- &lt;br /&gt;
|} &lt;br /&gt;
&#039;&#039;&#039;Notes&#039;&#039;&#039;: &lt;br /&gt;
* These profiles were developed and validated with the support of EDUMOL3D, Project [http://cercetare.bio.uaic.ro/grupuri/bioactive/content/grants/PED2024_mm.html PN-IV-P7-7.1-PED-2024-0343] financed by the Ministry of Research, Innovation and Digitization, [https://uefiscdi.gov.ro/ UEFISCDI], Romania.&lt;br /&gt;
* The profiles are a work in progress. Please check GitHub for updates. If you have suggestions for improvements, please drop a message at marius.mihasan(@)uaic.ro&lt;br /&gt;
&lt;br /&gt;
==== &#039;&#039;&#039;Note on multi-color printing &#039;&#039;&#039; ====&lt;br /&gt;
To our knowledge, only &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039; and &#039;&#039;&#039;Orca Slicer&#039;&#039;&#039; can automatically import color information from the &#039;&#039;&#039;.MTL&#039;&#039;&#039; file associated with the printable &#039;&#039;&#039;.OBJ&#039;&#039;&#039; generated by the Proteopedia &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool.  &lt;br /&gt;
At present, &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; does not support importing &#039;&#039;&#039;.MTL&#039;&#039;&#039; files directly.&lt;br /&gt;
&lt;br /&gt;
A practical workaround for &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; users is as follows:  &lt;br /&gt;
# Open the &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file in &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039;.  &lt;br /&gt;
#Verify or adjust the color mapping as needed.  &lt;br /&gt;
#Export the model as a generic &#039;&#039;&#039;.3MF&#039;&#039;&#039; file using the menu command:  &#039;&#039;File&#039;&#039; → &#039;&#039;Export&#039;&#039; → &#039;&#039;Export Generic 3MF...&#039;&#039;  &lt;br /&gt;
#Open the exported &#039;&#039;&#039;.3MF&#039;&#039;&#039; file in &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;. The color data will now be available under the &#039;&#039;&#039;Multimaterial Painting&#039;&#039;&#039; tool.&lt;br /&gt;
&lt;br /&gt;
This workflow preserves the original coloring assigned in Proteopedia and allows successful multi-color or multi-material printing on any capable 3D printer compatible with &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Other relevant resources ==&lt;br /&gt;
[[Print3D_models_gallery Proteopedia gallery of 3D printed models]] - examples of 3D printed molecular models from Proteopedia users.&lt;br /&gt;
&lt;br /&gt;
[https://3d.nih.gov/ NIH 3D Print Exchange] - an open, community-driven portal to download, share, and create bioscientific and medical 3D models, including for 3D printing.&lt;br /&gt;
  &lt;br /&gt;
[https://github.com/mariusmihasan/3DP-Jmol 3DP-Jmol] - the Jmol/JSmol behind the Print3D tool. Automatically generates 3D printable molecular models from structural data and can be easily integrated into web pages.&lt;br /&gt;
&lt;br /&gt;
[https://pdb101.rcsb.org/learn/3d-printing/pdb-structures-and-3d-printing 3D Printing on PDB101] - a quick guide on 3D printing molecular models and a small curated 3D models for education&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;If you print a model from Proteopedia, please share photos and feedback — let’s 3D print the whole Proteopedia!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386104</id>
		<title>Print3D help</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386104"/>
		<updated>2025-10-27T10:00:48Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== Proteopedia and 3D Printing ==&lt;br /&gt;
&lt;br /&gt;
Physical molecular models, by engaging both visual and tactile senses, provide an effective means of deepening the understanding of complex concepts in molecular biology and biochemistry. They allow students to perceive the three-dimensional organization of macromolecules, thereby enhancing comprehension of the relationship between structure and function &amp;lt;ref&amp;gt;PMID: 32590880&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 40214166&amp;lt;/ref&amp;gt;. Numerous studies have demonstrated that the use of tangible models in science education improves learning outcomes, fosters conceptual reasoning, and increases student engagement &amp;lt;ref&amp;gt;PMID: 27366318&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 26712513&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;Larsson, C., Tibell, L.A.E. Challenging Students’ Intuitions—the Influence of a Tangible Model of Virus Assembly on Students’ Conceptual Reasoning About the Process of Self-Assembly. Res Sci Educ 45, 663–690 (2015). [http://dx.doi.org/10.1007/s11165-014-9446-6 DOI: 110.1007/s11165-014-9446-6]&amp;lt;/ref&amp;gt;. The rapid development of 3D-printing technologies has made it possible to create customized and affordable molecular models  &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot;&amp;gt;PMID: 28362403&amp;lt;/ref&amp;gt; &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot;&amp;gt;PMID: 33755300&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 33384761&amp;lt;/ref&amp;gt;. &lt;br /&gt;
&lt;br /&gt;
Affordable desktop 3D printers can now be used to fabricate physical models from virtually any structure or scene on [[Proteopedia]]. This page provides an introduction to 3D printing, a step-by-step guide to generating printable files directly from [[Proteopedia]], and several tested printing profiles for common printers (e.g., Prusa Research, Bambu Lab, Creality, or Elegoo).&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== «3D Printing 101»: an introduction to 3D printing ==&lt;br /&gt;
3D printing, also known as &#039;&#039;additive manufacturing&#039;&#039;, builds physical objects layer by layer from digital designs. For more technical details please head for the excellent introductory article on [https://all3dp.com/2/what-is-3d-printing/ All3DP].  In structural biology education, 3D printing provides an affordable and accessible way to transform atomic coordinate data (e.g., from PDB, MOL or SDF files) into tangible molecular models that can be observed, handled, and discussed in class or laboratory settings.&lt;br /&gt;
&lt;br /&gt;
=== Printer Types: FDM vs. SLA/DLP ===&lt;br /&gt;
The two most accessible 3D-printing technologies that can be used to create molecular models are:&lt;br /&gt;
* &#039;&#039;&#039;FDM (Fused Deposition Modeling)&#039;&#039;&#039;&lt;br /&gt;
This method extrudes a heated thermoplastic filament (such as PLA, PETG or TPU) through a fine nozzle, depositing successive layers that form the model. FDM printers have the advantages of low cost, easy maintenance, wide availability, and being capable of printing large and colorful molecular models. This technology has a few limitations, such as: visible layer lines, lower surface resolution, and less suited for very small or intricate molecular details.&lt;br /&gt;
* &#039;&#039;&#039;SLA/DLP (Resin Printing)&#039;&#039;&#039;&lt;br /&gt;
This technique uses liquid photopolymer resin, cured layer by layer with ultraviolet light. SLA/DLP printers have the advantages of a very high resolution, smooth surfaces and are ideal for compact and detailed models (e.g., small proteins rendered as surface, ligands, or symmetric assemblies). This technology has its own limitations, such as higher material cost, post-processing requirements (washing and UV-curing), and the need for careful handling of resin.&lt;br /&gt;
&lt;br /&gt;
When choosing between FDM and SLA printers, model size and resolution are the key criteria: &#039;&#039;&#039;FDM&#039;&#039;&#039; is preferred for &#039;&#039;large, educational display models&#039;&#039;; &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; is optimal for &#039;&#039;small, precise structures&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
While FDM and SLA/DLP are the most widely used technologies in educational and research contexts due to their accessibility, other additive manufacturing methods also exist —such as &#039;&#039;Selective Laser Sintering&#039;&#039; (SLS), &#039;&#039;PolyJet&#039;&#039;, and &#039;&#039;Binder Jetting&#039;&#039;— each employing different materials and curing mechanisms. These industrial-grade techniques can produce highly detailed or multi-material parts but are generally more expensive and less accessible for classroom use. For an overview of major 3D-printing technologies, see [https://all3dp.com/1/types-of-3d-printers-3d-printing-technology/ All3DP: Complete Overview of the Types of 3D Printers]&lt;br /&gt;
&lt;br /&gt;
=== Single- vs. Multi-Material Printers ===&lt;br /&gt;
Most entry-level desktop 3D printers use a single filament or resin, producing models in one color or material. However, multi-material systems (such as [https://eu.store.bambulab.com/products/ams-multicolor-printing?from=home_web_top_navigation Bambu Lab AMS] and its variants or [https://www.prusa3d.com/category/original-prusa-mmu3/ Prusa MMU3]) can simultaneously print multiple filaments, enabling color-coded domains, subunits, or ligands directly in one print. For complex color information, users can also apply post-print color coding (painting or labeling) or print separate parts and assemble them manually.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A large FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A multi-material FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Small resin-printed models&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:GABAA_receptor.png|320px|center|thumb| GABAA receptor, [[6x3x]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Bacterial_Ribosome_multimaterial_FDM.png|348px|center|thumb| Bacterial 70S ribosome, [[4v5d]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Dna_insuline_sla.png|252px|center|thumb|DNA (left) and insulin (right) models, [[4bna]] and [[4ins]], scale at the bottom in cm]]&lt;br /&gt;
|-&lt;br /&gt;
|Trace Model of the GABAA receptor printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com] &lt;br /&gt;
|Surface model of the Bacterial 70S ribosome printed on a multi-material capable printer (BambuLab X1C AMS). Blue and violet are ribosomal proteins, orange and yellow are rRNAs, and black is tRNA. Printable files available on [https://www.printables.com/model/1430877-bacterial-70s-ribosome Printables.com]&lt;br /&gt;
|Balls and sticks and cartoon models of DNA (right) and insulin (left)&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== File Formats Used in 3D Printing ===&lt;br /&gt;
Proteopedia supports two export formats for generating printable molecular models:&lt;br /&gt;
*&#039;&#039;&#039;.STL&#039;&#039;&#039; (Stereolithography): the most common and universally compatible format; encodes only surface geometry, without color or texture information.&lt;br /&gt;
*&#039;&#039;&#039;.OBJ&#039;&#039;&#039; (Wavefront Object) with an associated &#039;&#039;&#039;.MTL&#039;&#039;&#039; (Material Template Library) files: includes both geometry and optional color/texture data; useful for color prints.&lt;br /&gt;
&lt;br /&gt;
Another widely adopted file format used in 3D printing is the &#039;&#039;&#039;.3MF&#039;&#039;&#039; (3D Manufacturing Format): a modern open standard that stores geometry, color, and multi-material metadata in a single file—recommended for advanced printers. For a more extensive pros and cons of different 3D printing file formats please see [https://all3dp.com/2/3d-file-format-3d-model-types/ The Main 3D Printing File Formats on all3dp]. &lt;br /&gt;
&lt;br /&gt;
STL is ideal for single-color models and maximum compatibility, while OBJ/MTL is recommended for multi-material workflows. 3MF files will be used in this tutorial to save the model and printing settings. &lt;br /&gt;
&lt;br /&gt;
Support in Proteopedia for these formats is based on the export capabilities of Jmol/JSmol; for details, see [http://wiki.jmol.org/index.php/File_formats/3D_Objects#STL STL] and [http://wiki.jmol.org/index.php/File_formats/3D_Objects#OBJ OBJ]&lt;br /&gt;
&lt;br /&gt;
== Overview of the 3D printing process ==&lt;br /&gt;
3D printing enables the transformation of atomic-level structural data into tangible macromolecular models that can be explored through both sight and touch.  &lt;br /&gt;
The process generally follows several main steps, each requiring specific types of software and hardware.&lt;br /&gt;
[[Image:3D_printing_workflow_v2.png|thumb|left|400px|Overview of the 3D printing workflow for generating physical molecular models.]]&lt;br /&gt;
	&lt;br /&gt;
=== Preparing the structure and generating a printable File ===&lt;br /&gt;
:The first stage involves creating a printable three-dimensional representation of the molecule. Some molecular-graphics programs such as [https://www.pymol.org/ PyMOL], [https://www.rbvi.ucsf.edu/chimerax/ UCSF ChimeraX], [https://molstar.org/Mol*], or [https://jmol.sourceforge.net/ Jmol] can be used not only to visualize a structure (from the Protein Data Bank or other sources), but also to export the resulting geometry in a .STL or .OBJ format. However, the default visualization styles of these programs are &#039;&#039;&#039;&#039;&#039;not directly suitable for 3D printing&#039;&#039;&#039;&#039;&#039;. Therefore, when preparing a model for fabrication, it is important to:&lt;br /&gt;
:* &#039;&#039;&#039;Select an appropriate molecular representation&#039;&#039;&#039; (e.g., surface, cartoon, sticks, spheres) depending on the pedagogical or structural feature you wish to highlight.  &lt;br /&gt;
:* &#039;&#039;&#039;Add struts or connectors&#039;&#039;&#039; to increase the mechanical stability of the model, especially for large complexes or long helices.  &lt;br /&gt;
:* &#039;&#039;&#039;Remove specific struts or pseudobonds&#039;&#039;&#039; when individual components — ligands, subunits, or cofactors — need to remain detachable.  &lt;br /&gt;
:* &#039;&#039;&#039;Adjust thickness&#039;&#039;&#039; of atoms, bonds, helices, and sheets to ensure adequate rigidity and printability (features thinner than the printer’s nozzle diameter or resin resolution may break).  &lt;br /&gt;
:* &#039;&#039;&#039;Apply meaningful coloring&#039;&#039;&#039; when preparing multi-material prints, for instance, to distinguish domains, chains, ligands or atoms.&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene that automates the process and enables users to effortlessly generate 3D-printable molecular models - more on that in the corresponding section [[#Generating printable files on Proteopedia|Generating printable files on Proteopedia]] within this page. For advanced users wanting to do this manually, we highly recommend two guides: &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot; /&amp;gt; and &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
=== Slicing the Model ===&lt;br /&gt;
Before printing, the STL file must be processed by a &#039;&#039;&#039;slicer&#039;&#039;&#039; — specialized software that converts 3D geometry into a series of horizontal layers. The slicer also generates &#039;&#039;&#039;G-code&#039;&#039;&#039;, the set of instructions that control the printer. These commands are printer-specific and include parameters such as extrusion speed, layer thickness, temperature, and movement. Together, they are usually stored as a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;.  &lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an FDM printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;number of perimeters&#039;&#039;&#039;, which affects mechanical strength and print time;&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines resolution and print duration;&lt;br /&gt;
:* &#039;&#039;&#039;infill density&#039;&#039;&#039;, which determines internal strength and affects print time;&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, temporary structures that hold overhanging regions;&lt;br /&gt;
:* &#039;&#039;&#039;print orientation&#039;&#039;&#039;, which influences surface quality, mechanical strength, and the amount of supports required.&lt;br /&gt;
:All these parameters make up a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. In this step, users must also select the material-specific parameters, or apply a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. More details on these profiles are provided later on this page.&lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines vertical resolution and print time; thinner layers produce smoother surfaces but significantly increase printing duration.&lt;br /&gt;
:* &#039;&#039;&#039;exposure time&#039;&#039;&#039;, which controls how long each layer is cured by UV light; optimal exposure ensures proper adhesion between layers without over-curing fine details.&lt;br /&gt;
:* &#039;&#039;&#039;bottom-layer exposure and count&#039;&#039;&#039;, which influence model adhesion to the build platform — longer exposures and additional base layers improve stability during printing.&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, which anchor the model to the build plate and prevent deformation during peeling; proper placement reduces surface marks and print failures.&lt;br /&gt;
:* &#039;&#039;&#039;model orientation&#039;&#039;&#039;, which affects surface quality, support contact area, and resin drainage; angling the model (typically 30–45°) minimizes suction forces and improves print reliability.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for FDM printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for resin printing&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:Insuline_sliced_prusa.gif|386px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|[[Image:Insuline_Sliced_SLA.gif|372px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|-&lt;br /&gt;
|Cartoon model of insulin sliced in PrusaSlicer and ready to be printed on FDM printers. The arrow shows the trajectory of the print head on a single slice or layer. Orange is the model, green are the supports. &lt;br /&gt;
|Cartoon model of insulin sliced in Elegoo SatelLite and ready to be printed on FDM printer.On the left, with blue is the model, with gray are the supports. On the right is the image on the UV screen. &lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== 3D Printing the Model ===&lt;br /&gt;
:The prepared G-code is then transferred to the 3D printer, either via an SD card, USB flash drive, or Wi-Fi connection. During printing, close observation of the first few layers is essential to ensure good adhesion to the build plate and a successful print. Total printing time depends on model size, selected layer height, and printer speed. &#039;&#039;Small peptide&#039;&#039; models may print in &#039;&#039;&#039;less than an hour&#039;&#039;&#039;, whereas l&#039;&#039;arge multimeric assemblies&#039;&#039; can require &#039;&#039;&#039;several hours or days&#039;&#039;&#039;. &#039;&#039;Multi-color&#039;&#039; or &#039;&#039;multi-material&#039;&#039; prints generally take &#039;&#039;&#039;longer&#039;&#039;&#039;, while &#039;&#039;SLA/DLP&#039;&#039; printers are generally &#039;&#039;&#039;faster&#039;&#039;&#039; due to their simultaneous layer exposure.&lt;br /&gt;
=== Post-Processing ===&lt;br /&gt;
:After printing, the model undergoes post-processing, which varies depending on the printing technology used:&lt;br /&gt;
:* For &#039;&#039;&#039;FDM prints&#039;&#039;&#039;, supports are removed mechanically, and surfaces can be smoothed by light sanding or polishing.&lt;br /&gt;
:* For &#039;&#039;&#039;resin prints&#039;&#039;&#039;, supports are removed mechanically, parts are washed in isopropanol to remove uncured resin and then exposed to UV light for final curing.&lt;br /&gt;
:Models printed in multiple parts can be assembled using cyanoacrylate or epoxy adhesive. Optional finishing steps (painting, labeling) can improve contrast between subunits or highlight functional regions.&lt;br /&gt;
&lt;br /&gt;
==Generating printable files on Proteopedia==&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene, enabling logged users to effortlessly generate 3D-printable molecular models directly from its pages. The tool is powered by [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;], a script that analyzes the structural data and automatically scales the model’s geometry to match the printable volume of a medium-size desktop 3D printer (e.g., Ender-3, 210×210×210 mm). During this process, the tool evaluates the molecular bounding box, atom radii, and bond lengths, then proportionally adjusts all dimensions to achieve a realistic and mechanically robust print scale — preserving scientific accuracy while ensuring manufacturability. For advanced users, [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;] may also be used in conjunction with the [https://jmol.sourceforge.net/ &#039;&#039;&#039;Jmol&#039;&#039;&#039;] program, providing full access to its scripting capabilities and advanced export features.&lt;br /&gt;
==Step-by-step guide for automatic generation of printable files on Proteopedia==&lt;br /&gt;
=== Open a structure and access the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool ===&lt;br /&gt;
Log in with your Proteopedia Username and password. Navigate to any Proteopedia page (for example, [[Introduction_to_protein_structure]]). The corresponding 3D structure will load in the viewer on the right.  &lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_button_in_Proteopedia.png|thumb|left|400px|The &#039;&#039;&#039;Print3D&#039;&#039;&#039; button on a Proteopedia page]]&lt;br /&gt;
&lt;br /&gt;
At the bottom of the structure display window, locate and click the &#039;&#039;&#039;Print3D&#039;&#039;&#039; button. The tool will launch and begin analyzing the current molecular structure.  &lt;br /&gt;
This process may take some time to complete, depending on the size of the structure.  &lt;br /&gt;
Please wait until the message &#039;&#039;&#039;Analyzing structure...&#039;&#039;&#039; disappears and the next page is displayed — this marks the start of the two-step printing workflow.&lt;br /&gt;
=== Select a molecular representation and a printing scale ===&lt;br /&gt;
In this new page, some user input is required. Each option includes a short explanation; the key steps are outlined below, but feel free to explore and adopt the settings that best fit your use case.&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step1.png|thumb|left|400px|Selecting molecular representation and printing scale]]&lt;br /&gt;
&lt;br /&gt;
(1) &#039;&#039;&#039;Choose a molecular representation&#039;&#039;&#039; from the &#039;&#039;&#039;Scheme&#039;&#039;&#039; list, based on your goal:&lt;br /&gt;
* &#039;&#039;&#039;Backbone&#039;&#039;&#039;, &#039;&#039;&#039;Trace&#039;&#039;&#039;, or &#039;&#039;&#039;Ribbon&#039;&#039;&#039; — to emphasize secondary structure (effective for teaching protein folds).&lt;br /&gt;
* &#039;&#039;&#039;Surface&#039;&#039;&#039; — to highlight molecular topology and binding sites.&lt;br /&gt;
* &#039;&#039;&#039;Ball &amp;amp; Stick&#039;&#039;&#039; — atom-level detail for ligands or small molecules; usually impractical for large proteins or complexes.&lt;br /&gt;
* &#039;&#039;&#039;Proteopedia Scene&#039;&#039;&#039; — attempts to render the current page’s scene directly; may not work for all scenes. This is not fully implemented and only available for a few users.&lt;br /&gt;
&#039;&#039;Note:&#039;&#039; Some representations may be unavailable for a given structure because they are not printable in a reliable way.&lt;br /&gt;
&lt;br /&gt;
(2) In the &#039;&#039;&#039;Printer&#039;&#039;&#039; section, select whether you want a &#039;&#039;&#039;single-color&#039;&#039;&#039; or a &#039;&#039;&#039;multi-color&#039;&#039;&#039; print.&lt;br /&gt;
&lt;br /&gt;
(3) In the &#039;&#039;&#039;Printer scale&#039;&#039;&#039; section, set the desired size of the printed model. The tool constrains safe sizes based on the chosen representation and displays the physical dimensions (mm). &#039;&#039;&#039;Important! Please note the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;printer scale value in %&amp;lt;/span&amp;gt; as it is going to be required downstream in the next section of this workflow, [[#Printing files from Proteopedia|Printing files from Proteopedia]]&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
(4) When ready, click the green &#039;&#039;&#039;Make printer files&#039;&#039;&#039; button. Please wait patiently until the  &#039;&#039;Generating files for 3D printing of...&#039;&#039; message disappears and the final step is displayed.&lt;br /&gt;
&lt;br /&gt;
===Download the .STL or .OBJ files===&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step2.png|thumb|left|400px|Final step in generating printable files]]&lt;br /&gt;
&lt;br /&gt;
In this final page, a 3D preview of the generated model is displayed.&lt;br /&gt;
You can use the mouse to rotate, zoom, and inspect the model from different angles. If the result meets your needs, click the green (A) &#039;&#039;&#039;Download files&#039;&#039;&#039; button and save the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive containing the &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; files on your computer. If your model needs further improvements, hit the green (B) &#039;&#039;&#039;Same structure&#039;&#039;&#039; button to return to the previous screen and adjust your settings.&lt;br /&gt;
&lt;br /&gt;
 maybe a movie is better- need to decide ?&lt;br /&gt;
&lt;br /&gt;
{{clear}}&lt;br /&gt;
== Printing files from Proteopedia ==&lt;br /&gt;
Unzipping the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive will produce the exported &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file, along with an optional &#039;&#039;&#039;.MTL&#039;&#039;&#039; material file. &lt;br /&gt;
=== Using 3D printing services ===&lt;br /&gt;
If you do not have a 3D printer, you can still obtain physical models by using locally available 3D-printing services. Just search on [https://www.google.com/maps Google Maps] with the term  &#039;&#039;&#039;3D printing&#039;&#039;&#039; in your area. Here is short list of well-known 3D Printing service providers that may also ship worldwide: &lt;br /&gt;
&lt;br /&gt;
* [https://www.shapeways.com/ &#039;&#039;&#039;Shapeways&#039;&#039;&#039;] — global service offering a wide range of materials and colors. Educational discounts are available through their academic program.&lt;br /&gt;
* [https://www.sculpteo.com/en/ &#039;&#039;&#039;Sculpteo&#039;&#039;&#039;] — Europe-based provider offering fast turnaround and many printing technologies, including resin and polymer options.&lt;br /&gt;
* [https://www.xometry.com/capabilities/3d-printing-service &#039;&#039;&#039;Xometry&#039;&#039;&#039;] — large international network providing access to industrial-grade printing methods such as FDM, SLA, SLS, and DMLS.&lt;br /&gt;
* [https://craftcloud3d.com/ &#039;&#039;&#039;Craftcloud&#039;&#039;&#039;] — an aggregator that compares multiple providers and finds the best price and lead time for your uploaded model.&lt;br /&gt;
&lt;br /&gt;
When contacting a printing service, provide the exported files together with the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value in %&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ([[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). It is also advisable to share the link to this Proteopedia page so that the operator understands the peculiarities of printing molecular models. &lt;br /&gt;
&lt;br /&gt;
=== Using a desktop 3D printer ===&lt;br /&gt;
&lt;br /&gt;
Before importing the .STL or .OBJ file into your slicer software, it is recommended to inspect and, if necessary, repair the model to ensure printability. Common issues include non-manifold geometry, intersecting faces, and missing surfaces.  The example below demonstrates how to use [https://www.blender.org/ &#039;&#039;&#039;Blender&#039;&#039;&#039;] together with its [https://extensions.blender.org/add-ons/print3d-toolbox/ &#039;&#039;&#039;3D Print Toolbox extension&#039;&#039;&#039;] to improve the printability of the .STL and .OBJ files generated with the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in [[Proteopedia]]. &#039;&#039;&#039;Important note&#039;&#039;&#039;: The repair process is largely automated but may introduce artifacts. Carefully inspect the corrected model for any missing or distorted sections, atoms, or bonds, and determine whether these omissions affect the intended purpose of the printed model.  &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for single color or resin printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for multi-color FDM printing&lt;br /&gt;
|-&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=k6u-5JnoP-c&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=OCisrIZMIDM&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|}  &lt;br /&gt;
&lt;br /&gt;
Once the repaired &#039;&#039;&#039;.STL or .OBJ&#039;&#039;&#039; file is ready, it can be imported into your slicer software. In this step, you will prepare the file for printing by applying appropriate printer, filament, and print-settings profiles.&lt;br /&gt;
&lt;br /&gt;
*Apply the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value (%)&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ( [[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). This step ensures that the model fits your print bed and maintains structural integrity during printing. The location of the scale (%) input field varies depending on the slicer software you are using.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Orient the model on the print bed&#039;&#039;&#039; so that its largest, flattest surface rests on the bed. This minimizes the need for supports and improves adhesion. If your slicer includes an Auto Orient or Auto Arrange function, use it to optimize placement. (&#039;&#039;Hint&#039;&#039;: Bambu Studio and Orca Slicer include this feature, Ultimaker Cura has a [https://marketplace.ultimaker.com/app/cura/plugins/nallath/OrientationPlugin Auto-Orientation plugin] available, while PrusaSlicer currently does not.)&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Select the printer&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that matches your device.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Choose the material&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; corresponding to the filament type (e.g., PLA, PETG, TPU) and manufacturer you intend to use.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Adjust the printing parameters&#039;&#039;&#039; by selecting a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that defines layer height, infill, speed, and support options.&lt;br /&gt;
&lt;br /&gt;
In most cases, the default &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; and &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; provided by the slicer are sufficient. However, molecular models often include overhangs, thin connections, and complex internal geometries, which require additional supports and reinforced perimeters to ensure structural stability. For this reason, the default &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; may not yield optimal results.&lt;br /&gt;
&lt;br /&gt;
Validated printing profiles for the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool are available for several printer models. These profiles provide optimized settings that produce sturdy models, reduce material consumption, and shorten print time, ensuring consistent and reliable results. Three distinct profiles are supplied, corresponding to major molecular representations: &#039;&#039;&#039;balls and sticks&#039;&#039;&#039;, &#039;&#039;&#039;surface&#039;&#039;&#039;, and &#039;&#039;&#039;cartoon&#039;&#039;&#039;. The &#039;&#039;&#039;cartoon&#039;&#039;&#039; profile is also suitable for &#039;&#039;&#039;backbone&#039;&#039;&#039;, &#039;&#039;&#039;trace&#039;&#039;&#039;, and &#039;&#039;&#039;ribbon&#039;&#039;&#039; representations. For some printers, each profile is supplied in two variants, one using standard supports and one using tree or organic supports. In the case of multi-material printers, profiles for printing with soluble support and soluble interface are also provided.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer brand and model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Profiles provided as / Slicer&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer Type, nozle size and multi-material support&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |GitHub with profiles&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to import profiles into Slicer&lt;br /&gt;
|-&lt;br /&gt;
|Original Prusa Core One&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer ]&lt;br /&gt;
|FDM / 0.4 mm / yes, 5 colors, if MMU3 installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/Prusa%20CoreOne CoreOne]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab A1Mini&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, 4 colors if AMS Lite is installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/BambuLab%20A1Mini AiMini]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab X1 Carbon&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, up to 16 colors if multiple AMS are installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ca92e7de9c72505c1b9b09e912ad177341cabc9a/BambuLab%20X1C X1Carbon]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|- &lt;br /&gt;
|Original Prusa MK3S+&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/7a7ee68d1e19f063600f53def49a99dfefbc595d/Prusa%20MK3S%2B MK3S+]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 5 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/a653c7cc6b3dec86b90117cc450d1883cc4a80bd/Ender-5-Pro Ender5Pro]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 3 v2 with a ENDERIDEX kit&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / yes, IDEX, two filaments&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/c2c74f1261a42c160e7e3898a407f21465de2ca7/Ender3-IDEX Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Kingroon KPS3 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ea733b2d05020b99f91c92f71a039c5ba8e54108/Kingroon-KPS3-Pro Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Elegoo Mars 5 Ultra&lt;br /&gt;
|no profile needed, just be sure to add supports / [https://www.elegoo.com/pages/satellite-3d-slicer?srsltid=AfmBOopMQGHgHycHMFOZALzOIC8z7bVlSHjL_jj2ShYR4QkowYKmKzUx ELEGOO SatelLite]&lt;br /&gt;
|resin / - / no&lt;br /&gt;
|&lt;br /&gt;
|no profile needed, default settings worked, just be sure to add supports. EVO supports worked well enough.  Post-processing steps: 1)washing: at least 10 min. 2) support removal 3)curring: at least 10 min on a Elegoo Mercury Plus V3.0&lt;br /&gt;
|- &lt;br /&gt;
|} &lt;br /&gt;
&#039;&#039;&#039;Notes&#039;&#039;&#039;: &lt;br /&gt;
* These profiles were developed and validated with the support of EDUMOL3D, Project [http://cercetare.bio.uaic.ro/grupuri/bioactive/content/grants/PED2024_mm.html PN-IV-P7-7.1-PED-2024-0343] financed by the Ministry of Research, Innovation and Digitization, [https://uefiscdi.gov.ro/ UEFISCDI], Romania.&lt;br /&gt;
* The profiles are a work in progress. Please check GitHub for updates. If you have suggestions for improvements, please drop a message at marius.mihasan(@)uaic.ro&lt;br /&gt;
&lt;br /&gt;
==== &#039;&#039;&#039;Note on multi-color printing &#039;&#039;&#039; ====&lt;br /&gt;
To our knowledge, only &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039; and &#039;&#039;&#039;Orca Slicer&#039;&#039;&#039; can automatically import color information from the &#039;&#039;&#039;.MTL&#039;&#039;&#039; file associated with the printable &#039;&#039;&#039;.OBJ&#039;&#039;&#039; generated by the Proteopedia &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool.  &lt;br /&gt;
At present, &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; does not support importing &#039;&#039;&#039;.MTL&#039;&#039;&#039; files directly.&lt;br /&gt;
&lt;br /&gt;
A practical workaround for &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; users is as follows:  &lt;br /&gt;
# Open the &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file in &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039;.  &lt;br /&gt;
#Verify or adjust the color mapping as needed.  &lt;br /&gt;
#Export the model as a generic &#039;&#039;&#039;.3MF&#039;&#039;&#039; file using the menu command:  &#039;&#039;File&#039;&#039; → &#039;&#039;Export&#039;&#039; → &#039;&#039;Export Generic 3MF...&#039;&#039;  &lt;br /&gt;
#Open the exported &#039;&#039;&#039;.3MF&#039;&#039;&#039; file in &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;. The color data will now be available under the &#039;&#039;&#039;Multimaterial Painting&#039;&#039;&#039; tool.&lt;br /&gt;
&lt;br /&gt;
This workflow preserves the original coloring assigned in Proteopedia and allows successful multi-color or multi-material printing on any capable 3D printer compatible with &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Other relevant resources ==&lt;br /&gt;
[https://proteopedia.org/wiki/index.php/User:Marius_Mihasan/Print3D_models_gallery Proteopedia gallery of 3D printed models] - examples of 3D printed molecular models from Proteopedia users.&lt;br /&gt;
&lt;br /&gt;
[https://3d.nih.gov/ NIH 3D Print Exchange] - an open, community-driven portal to download, share, and create bioscientific and medical 3D models, including for 3D printing.&lt;br /&gt;
  &lt;br /&gt;
[https://github.com/mariusmihasan/3DP-Jmol 3DP-Jmol] - the Jmol/JSmol behind the Print3D tool. Automatically generates 3D printable molecular models from structural data and can be easily integrated into web pages.&lt;br /&gt;
&lt;br /&gt;
[https://pdb101.rcsb.org/learn/3d-printing/pdb-structures-and-3d-printing 3D Printing on PDB101] - a quick guide on 3D printing molecular models and a small curated 3D models for education&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;If you print a model from Proteopedia, please share photos and feedback — let’s 3D print the whole Proteopedia!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386103</id>
		<title>Print3D help</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386103"/>
		<updated>2025-10-27T09:59:45Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== Proteopedia and 3D Printing ==&lt;br /&gt;
&lt;br /&gt;
Physical molecular models, by engaging both visual and tactile senses, provide an effective means of deepening the understanding of complex concepts in molecular biology and biochemistry. They allow students to perceive the three-dimensional organization of macromolecules, thereby enhancing comprehension of the relationship between structure and function &amp;lt;ref&amp;gt;PMID: 32590880&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 40214166&amp;lt;/ref&amp;gt;. Numerous studies have demonstrated that the use of tangible models in science education improves learning outcomes, fosters conceptual reasoning, and increases student engagement &amp;lt;ref&amp;gt;PMID: 27366318&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 26712513&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;Larsson, C., Tibell, L.A.E. Challenging Students’ Intuitions—the Influence of a Tangible Model of Virus Assembly on Students’ Conceptual Reasoning About the Process of Self-Assembly. Res Sci Educ 45, 663–690 (2015). [http://dx.doi.org/10.1007/s11165-014-9446-6 DOI: 110.1007/s11165-014-9446-6]&amp;lt;/ref&amp;gt;. The rapid development of 3D-printing technologies has made it possible to create customized and affordable molecular models  &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot;&amp;gt;PMID: 28362403&amp;lt;/ref&amp;gt; &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot;&amp;gt;PMID: 33755300&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 33384761&amp;lt;/ref&amp;gt;. &lt;br /&gt;
&lt;br /&gt;
Affordable desktop 3D printers can now be used to fabricate physical models from virtually any structure or scene on [[Proteopedia]]. This page provides an introduction to 3D printing, a step-by-step guide to generating printable files directly from [[Proteopedia]], and several tested printing profiles for common printers (e.g., Prusa Research, Bambu Lab, Creality, or Elegoo).&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== «3D Printing 101»: an introduction to 3D printing ==&lt;br /&gt;
3D printing, also known as &#039;&#039;additive manufacturing&#039;&#039;, builds physical objects layer by layer from digital designs. For more technical details please head for the excellent introductory article on [https://all3dp.com/2/what-is-3d-printing/ All3DP].  In structural biology education, 3D printing provides an affordable and accessible way to transform atomic coordinate data (e.g., from PDB, MOL or SDF files) into tangible molecular models that can be observed, handled, and discussed in class or laboratory settings.&lt;br /&gt;
&lt;br /&gt;
=== Printer Types: FDM vs. SLA/DLP ===&lt;br /&gt;
The two most accessible 3D-printing technologies that can be used to create molecular models are:&lt;br /&gt;
* &#039;&#039;&#039;FDM (Fused Deposition Modeling)&#039;&#039;&#039;&lt;br /&gt;
This method extrudes a heated thermoplastic filament (such as PLA, PETG or TPU) through a fine nozzle, depositing successive layers that form the model. FDM printers have the advantages of low cost, easy maintenance, wide availability, and being capable of printing large and colorful molecular models. This technology has a few limitations, such as: visible layer lines, lower surface resolution, and less suited for very small or intricate molecular details.&lt;br /&gt;
* &#039;&#039;&#039;SLA/DLP (Resin Printing)&#039;&#039;&#039;&lt;br /&gt;
This technique uses liquid photopolymer resin, cured layer by layer with ultraviolet light. SLA/DLP printers have the advantages of a very high resolution, smooth surfaces and are ideal for compact and detailed models (e.g., small proteins rendered as surface, ligands, or symmetric assemblies). This technology has its own limitations, such as higher material cost, post-processing requirements (washing and UV-curing), and the need for careful handling of resin.&lt;br /&gt;
&lt;br /&gt;
When choosing between FDM and SLA printers, model size and resolution are the key criteria: &#039;&#039;&#039;FDM&#039;&#039;&#039; is preferred for &#039;&#039;large, educational display models&#039;&#039;; &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; is optimal for &#039;&#039;small, precise structures&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
While FDM and SLA/DLP are the most widely used technologies in educational and research contexts due to their accessibility, other additive manufacturing methods also exist —such as &#039;&#039;Selective Laser Sintering&#039;&#039; (SLS), &#039;&#039;PolyJet&#039;&#039;, and &#039;&#039;Binder Jetting&#039;&#039;— each employing different materials and curing mechanisms. These industrial-grade techniques can produce highly detailed or multi-material parts but are generally more expensive and less accessible for classroom use. For an overview of major 3D-printing technologies, see [https://all3dp.com/1/types-of-3d-printers-3d-printing-technology/ All3DP: Complete Overview of the Types of 3D Printers]&lt;br /&gt;
&lt;br /&gt;
=== Single- vs. Multi-Material Printers ===&lt;br /&gt;
Most entry-level desktop 3D printers use a single filament or resin, producing models in one color or material. However, multi-material systems (such as [https://eu.store.bambulab.com/products/ams-multicolor-printing?from=home_web_top_navigation Bambu Lab AMS] and its variants or [https://www.prusa3d.com/category/original-prusa-mmu3/ Prusa MMU3]) can simultaneously print multiple filaments, enabling color-coded domains, subunits, or ligands directly in one print. For complex color information, users can also apply post-print color coding (painting or labeling) or print separate parts and assemble them manually.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A large FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A multi-material FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Small resin-printed models&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:GABAA_receptor.png|320px|center|thumb| GABAA receptor, [[6x3x]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Bacterial_Ribosome_multimaterial_FDM.png|348px|center|thumb| Bacterial 70S ribosome, [[4v5d]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Dna_insuline_sla.png|252px|center|thumb|DNA (left) and insulin (right) models, [[4bna]] and [[4ins]], scale at the bottom in cm]]&lt;br /&gt;
|-&lt;br /&gt;
|Trace Model of the GABAA receptor printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com] &lt;br /&gt;
|Surface model of the Bacterial 70S ribosome printed on a multi-material capable printer (BambuLab X1C AMS). Blue and violet are ribosomal proteins, orange and yellow are rRNAs, and black is tRNA. Printable files available on [https://www.printables.com/model/1430877-bacterial-70s-ribosome Printables.com]&lt;br /&gt;
|Balls and sticks and cartoon models of DNA (right) and insulin (left)&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== File Formats Used in 3D Printing ===&lt;br /&gt;
Proteopedia supports two export formats for generating printable molecular models:&lt;br /&gt;
*&#039;&#039;&#039;.STL&#039;&#039;&#039; (Stereolithography): the most common and universally compatible format; encodes only surface geometry, without color or texture information.&lt;br /&gt;
*&#039;&#039;&#039;.OBJ&#039;&#039;&#039; (Wavefront Object) with an associated &#039;&#039;&#039;.MTL&#039;&#039;&#039; (Material Template Library) files: includes both geometry and optional color/texture data; useful for color prints.&lt;br /&gt;
&lt;br /&gt;
Another widely adopted file format used in 3D printing is the &#039;&#039;&#039;.3MF&#039;&#039;&#039; (3D Manufacturing Format): a modern open standard that stores geometry, color, and multi-material metadata in a single file—recommended for advanced printers. For a more extensive pros and cons of different 3D printing file formats please see [https://all3dp.com/2/3d-file-format-3d-model-types/ The Main 3D Printing File Formats on all3dp]. &lt;br /&gt;
&lt;br /&gt;
STL is ideal for single-color models and maximum compatibility, while OBJ/MTL is recommended for multi-material workflows. 3MF files will be used in this tutorial to save the model and printing settings. &lt;br /&gt;
&lt;br /&gt;
Support in Proteopedia for these formats is based on the export capabilities of Jmol/JSmol; for details, see [http://wiki.jmol.org/index.php/File_formats/3D_Objects#STL STL] and [http://wiki.jmol.org/index.php/File_formats/3D_Objects#OBJ OBJ]&lt;br /&gt;
&lt;br /&gt;
== Overview of the 3D printing process ==&lt;br /&gt;
3D printing enables the transformation of atomic-level structural data into tangible macromolecular models that can be explored through both sight and touch.  &lt;br /&gt;
The process generally follows several main steps, each requiring specific types of software and hardware.&lt;br /&gt;
[[Image:3D_printing_workflow_v2.png|thumb|left|400px|Overview of the 3D printing workflow for generating physical molecular models.]]&lt;br /&gt;
	&lt;br /&gt;
=== Preparing the structure and generating a printable File ===&lt;br /&gt;
:The first stage involves creating a printable three-dimensional representation of the molecule. Some molecular-graphics programs such as [https://www.pymol.org/ PyMOL], [https://www.rbvi.ucsf.edu/chimerax/ UCSF ChimeraX], [https://molstar.org/Mol*], or [https://jmol.sourceforge.net/ Jmol] can be used not only to visualize a structure (from the Protein Data Bank or other sources), but also to export the resulting geometry in a .STL or .OBJ format. However, the default visualization styles of these programs are &#039;&#039;&#039;&#039;&#039;not directly suitable for 3D printing&#039;&#039;&#039;&#039;&#039;. Therefore, when preparing a model for fabrication, it is important to:&lt;br /&gt;
:* &#039;&#039;&#039;Select an appropriate molecular representation&#039;&#039;&#039; (e.g., surface, cartoon, sticks, spheres) depending on the pedagogical or structural feature you wish to highlight.  &lt;br /&gt;
:* &#039;&#039;&#039;Add struts or connectors&#039;&#039;&#039; to increase the mechanical stability of the model, especially for large complexes or long helices.  &lt;br /&gt;
:* &#039;&#039;&#039;Remove specific struts or pseudobonds&#039;&#039;&#039; when individual components — ligands, subunits, or cofactors — need to remain detachable.  &lt;br /&gt;
:* &#039;&#039;&#039;Adjust thickness&#039;&#039;&#039; of atoms, bonds, helices, and sheets to ensure adequate rigidity and printability (features thinner than the printer’s nozzle diameter or resin resolution may break).  &lt;br /&gt;
:* &#039;&#039;&#039;Apply meaningful coloring&#039;&#039;&#039; when preparing multi-material prints, for instance, to distinguish domains, chains, ligands or atoms.&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene that automates the process and enables users to effortlessly generate 3D-printable molecular models - more on that in the corresponding section [[#Generating printable files on Proteopedia|Generating printable files on Proteopedia]] within this page. For advanced users wanting to do this manually, we highly recommend two guides: &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot; /&amp;gt; and &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
=== Slicing the Model ===&lt;br /&gt;
Before printing, the STL file must be processed by a &#039;&#039;&#039;slicer&#039;&#039;&#039; — specialized software that converts 3D geometry into a series of horizontal layers. The slicer also generates &#039;&#039;&#039;G-code&#039;&#039;&#039;, the set of instructions that control the printer. These commands are printer-specific and include parameters such as extrusion speed, layer thickness, temperature, and movement. Together, they are usually stored as a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;.  &lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an FDM printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;number of perimeters&#039;&#039;&#039;, which affects mechanical strength and print time;&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines resolution and print duration;&lt;br /&gt;
:* &#039;&#039;&#039;infill density&#039;&#039;&#039;, which determines internal strength and affects print time;&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, temporary structures that hold overhanging regions;&lt;br /&gt;
:* &#039;&#039;&#039;print orientation&#039;&#039;&#039;, which influences surface quality, mechanical strength, and the amount of supports required.&lt;br /&gt;
:All these parameters make up a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. In this step, users must also select the material-specific parameters, or apply a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. More details on these profiles are provided later on this page.&lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines vertical resolution and print time; thinner layers produce smoother surfaces but significantly increase printing duration.&lt;br /&gt;
:* &#039;&#039;&#039;exposure time&#039;&#039;&#039;, which controls how long each layer is cured by UV light; optimal exposure ensures proper adhesion between layers without over-curing fine details.&lt;br /&gt;
:* &#039;&#039;&#039;bottom-layer exposure and count&#039;&#039;&#039;, which influence model adhesion to the build platform — longer exposures and additional base layers improve stability during printing.&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, which anchor the model to the build plate and prevent deformation during peeling; proper placement reduces surface marks and print failures.&lt;br /&gt;
:* &#039;&#039;&#039;model orientation&#039;&#039;&#039;, which affects surface quality, support contact area, and resin drainage; angling the model (typically 30–45°) minimizes suction forces and improves print reliability.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for FDM printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for resin printing&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:Insuline_sliced_prusa.gif|386px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|[[Image:Insuline_Sliced_SLA.gif|372px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|-&lt;br /&gt;
|Cartoon model of insulin sliced in PrusaSlicer and ready to be printed on FDM printers. The arrow shows the trajectory of the print head on a single slice or layer. Orange is the model, green are the supports. &lt;br /&gt;
|Cartoon model of insulin sliced in Elegoo SatelLite and ready to be printed on FDM printer.On the left, with blue is the model, with gray are the supports. On the right is the image on the UV screen. &lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== 3D Printing the Model ===&lt;br /&gt;
:The prepared G-code is then transferred to the 3D printer, either via an SD card, USB flash drive, or Wi-Fi connection. During printing, close observation of the first few layers is essential to ensure good adhesion to the build plate and a successful print. Total printing time depends on model size, selected layer height, and printer speed. &#039;&#039;Small peptide&#039;&#039; models may print in &#039;&#039;&#039;less than an hour&#039;&#039;&#039;, whereas l&#039;&#039;arge multimeric assemblies&#039;&#039; can require &#039;&#039;&#039;several hours or days&#039;&#039;&#039;. &#039;&#039;Multi-color&#039;&#039; or &#039;&#039;multi-material&#039;&#039; prints generally take &#039;&#039;&#039;longer&#039;&#039;&#039;, while &#039;&#039;SLA/DLP&#039;&#039; printers are generally &#039;&#039;&#039;faster&#039;&#039;&#039; due to their simultaneous layer exposure.&lt;br /&gt;
=== Post-Processing ===&lt;br /&gt;
:After printing, the model undergoes post-processing, which varies depending on the printing technology used:&lt;br /&gt;
:* For &#039;&#039;&#039;FDM prints&#039;&#039;&#039;, supports are removed mechanically, and surfaces can be smoothed by light sanding or polishing.&lt;br /&gt;
:* For &#039;&#039;&#039;resin prints&#039;&#039;&#039;, supports are removed mechanically, parts are washed in isopropanol to remove uncured resin and then exposed to UV light for final curing.&lt;br /&gt;
:Models printed in multiple parts can be assembled using cyanoacrylate or epoxy adhesive. Optional finishing steps (painting, labeling) can improve contrast between subunits or highlight functional regions.&lt;br /&gt;
&lt;br /&gt;
==Generating printable files on Proteopedia==&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene, enabling logged users to effortlessly generate 3D-printable molecular models directly from its pages. The tool is powered by [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;], a script that analyzes the structural data and automatically scales the model’s geometry to match the printable volume of a medium-size desktop 3D printer (e.g., Ender-3, 210×210×210 mm). During this process, the tool evaluates the molecular bounding box, atom radii, and bond lengths, then proportionally adjusts all dimensions to achieve a realistic and mechanically robust print scale — preserving scientific accuracy while ensuring manufacturability. For advanced users, [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;] may also be used in conjunction with the [https://jmol.sourceforge.net/ &#039;&#039;&#039;Jmol&#039;&#039;&#039;] program, providing full access to its scripting capabilities and advanced export features.&lt;br /&gt;
==Step-by-step guide for automatic generation of printable files on Proteopedia==&lt;br /&gt;
=== Open a structure and access the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool ===&lt;br /&gt;
Log in with your Proteopedia Username and password. Navigate to any Proteopedia page (for example, [[Introduction_to_protein_structure]]). The corresponding 3D structure will load in the viewer on the right.  &lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_button_in_Proteopedia.png|thumb|left|400px|The &#039;&#039;&#039;Print3D&#039;&#039;&#039; button on a Proteopedia page]]&lt;br /&gt;
&lt;br /&gt;
At the bottom of the structure display window, locate and click the &#039;&#039;&#039;Print3D&#039;&#039;&#039; button. The tool will launch and begin analyzing the current molecular structure.  &lt;br /&gt;
This process may take some time to complete, depending on the size of the structure.  &lt;br /&gt;
Please wait until the message &#039;&#039;&#039;Analyzing structure...&#039;&#039;&#039; disappears and the next page is displayed — this marks the start of the two-step printing workflow.&lt;br /&gt;
=== Select a molecular representation and a printing scale ===&lt;br /&gt;
In this new page, some user input is required. Each option includes a short explanation; the key steps are outlined below, but feel free to explore and adopt the settings that best fit your use case.&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step1.png|thumb|left|400px|Selecting molecular representation and printing scale]]&lt;br /&gt;
&lt;br /&gt;
(1) &#039;&#039;&#039;Choose a molecular representation&#039;&#039;&#039; from the &#039;&#039;&#039;Scheme&#039;&#039;&#039; list, based on your goal:&lt;br /&gt;
* &#039;&#039;&#039;Backbone&#039;&#039;&#039;, &#039;&#039;&#039;Trace&#039;&#039;&#039;, or &#039;&#039;&#039;Ribbon&#039;&#039;&#039; — to emphasize secondary structure (effective for teaching protein folds).&lt;br /&gt;
* &#039;&#039;&#039;Surface&#039;&#039;&#039; — to highlight molecular topology and binding sites.&lt;br /&gt;
* &#039;&#039;&#039;Ball &amp;amp; Stick&#039;&#039;&#039; — atom-level detail for ligands or small molecules; usually impractical for large proteins or complexes.&lt;br /&gt;
* &#039;&#039;&#039;Proteopedia Scene&#039;&#039;&#039; — attempts to render the current page’s scene directly; may not work for all scenes. This is not fully implemented and only available for a few users.&lt;br /&gt;
&#039;&#039;Note:&#039;&#039; Some representations may be unavailable for a given structure because they are not printable in a reliable way.&lt;br /&gt;
&lt;br /&gt;
(2) In the &#039;&#039;&#039;Printer&#039;&#039;&#039; section, select whether you want a &#039;&#039;&#039;single-color&#039;&#039;&#039; or a &#039;&#039;&#039;multi-color&#039;&#039;&#039; print.&lt;br /&gt;
&lt;br /&gt;
(3) In the &#039;&#039;&#039;Printer scale&#039;&#039;&#039; section, set the desired size of the printed model. The tool constrains safe sizes based on the chosen representation and displays the physical dimensions (mm). &#039;&#039;&#039;Important! Please note the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;printer scale value in %&amp;lt;/span&amp;gt; as it is going to be required downstream in the next section of this workflow, [[#Printing files from Proteopedia|Printing files from Proteopedia]]&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
(4) When ready, click the green &#039;&#039;&#039;Make printer files&#039;&#039;&#039; button. Please wait patiently until the  &#039;&#039;Generating files for 3D printing of...&#039;&#039; message disappears and the final step is displayed.&lt;br /&gt;
&lt;br /&gt;
===Download the .STL or .OBJ files===&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step2.png|thumb|left|400px|Final step in generating printable files]]&lt;br /&gt;
&lt;br /&gt;
In this final page, a 3D preview of the generated model is displayed.&lt;br /&gt;
You can use the mouse to rotate, zoom, and inspect the model from different angles. If the result meets your needs, click the green (A) &#039;&#039;&#039;Download files&#039;&#039;&#039; button and save the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive containing the &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; files on your computer. If your model needs further improvements, hit the green (B) &#039;&#039;&#039;Same structure&#039;&#039;&#039; button to return to the previous screen and adjust your settings.&lt;br /&gt;
&lt;br /&gt;
 maybe a movie is better- need to decide ?&lt;br /&gt;
&lt;br /&gt;
{{clear}}&lt;br /&gt;
== Printing files from Proteopedia ==&lt;br /&gt;
Unzipping the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive will produce the exported &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file, along with an optional &#039;&#039;&#039;.MTL&#039;&#039;&#039; material file. &lt;br /&gt;
=== Using 3D printing services ===&lt;br /&gt;
If you do not have a 3D printer, you can still obtain physical models by using locally available 3D-printing services. Just search on [https://www.google.com/maps Google Maps] with the term  &#039;&#039;&#039;3D printing&#039;&#039;&#039; in your area. Here is short list of well-known 3D Printing service providers that may also ship worldwide: &lt;br /&gt;
&lt;br /&gt;
* [https://www.shapeways.com/ &#039;&#039;&#039;Shapeways&#039;&#039;&#039;] — global service offering a wide range of materials and colors. Educational discounts are available through their academic program.&lt;br /&gt;
* [https://www.sculpteo.com/en/ &#039;&#039;&#039;Sculpteo&#039;&#039;&#039;] — Europe-based provider offering fast turnaround and many printing technologies, including resin and polymer options.&lt;br /&gt;
* [https://www.xometry.com/capabilities/3d-printing-service &#039;&#039;&#039;Xometry&#039;&#039;&#039;] — large international network providing access to industrial-grade printing methods such as FDM, SLA, SLS, and DMLS.&lt;br /&gt;
* [https://craftcloud3d.com/ &#039;&#039;&#039;Craftcloud&#039;&#039;&#039;] — an aggregator that compares multiple providers and finds the best price and lead time for your uploaded model.&lt;br /&gt;
&lt;br /&gt;
When contacting a printing service, provide the exported files together with the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value in %&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ([[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). It is also advisable to share the link to this Proteopedia page so that the operator understands the peculiarities of printing molecular models. &lt;br /&gt;
&lt;br /&gt;
=== Using a desktop 3D printer ===&lt;br /&gt;
&lt;br /&gt;
Before importing the .STL or .OBJ file into your slicer software, it is recommended to inspect and, if necessary, repair the model to ensure printability. Common issues include non-manifold geometry, intersecting faces, and missing surfaces.  The example below demonstrates how to use [https://www.blender.org/ &#039;&#039;&#039;Blender&#039;&#039;&#039;] together with its [https://extensions.blender.org/add-ons/print3d-toolbox/ &#039;&#039;&#039;3D Print Toolbox extension&#039;&#039;&#039;] to improve the printability of the .STL and .OBJ files generated with the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in [[Proteopedia]]. &#039;&#039;&#039;Important note&#039;&#039;&#039;: The repair process is largely automated but may introduce artifacts. Carefully inspect the corrected model for any missing or distorted sections, atoms, or bonds, and determine whether these omissions affect the intended purpose of the printed model.  &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for single color or resin printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for multi-color FDM printing&lt;br /&gt;
|-&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=k6u-5JnoP-c&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=OCisrIZMIDM&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|}  &lt;br /&gt;
&lt;br /&gt;
Once the repaired &#039;&#039;&#039;.STL or .OBJ&#039;&#039;&#039; file is ready, it can be imported into your slicer software. In this step, you will prepare the file for printing by applying appropriate printer, filament, and print-settings profiles.&lt;br /&gt;
&lt;br /&gt;
*Apply the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value (%)&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ( [[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). This step ensures that the model fits your print bed and maintains structural integrity during printing. The location of the scale (%) input field varies depending on the slicer software you are using.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Orient the model on the print bed&#039;&#039;&#039; so that its largest, flattest surface rests on the bed. This minimizes the need for supports and improves adhesion. If your slicer includes an Auto Orient or Auto Arrange function, use it to optimize placement. (&#039;&#039;Hint&#039;&#039;: Bambu Studio and Orca Slicer include this feature, Ultimaker Cura has a [https://marketplace.ultimaker.com/app/cura/plugins/nallath/OrientationPlugin Auto-Orientation plugin] available, while PrusaSlicer currently does not.)&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Select the printer&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that matches your device.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Choose the material&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; corresponding to the filament type (e.g., PLA, PETG, TPU) and manufacturer you intend to use.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Adjust the printing parameters&#039;&#039;&#039; by selecting a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that defines layer height, infill, speed, and support options.&lt;br /&gt;
&lt;br /&gt;
In most cases, the default &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; and &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; provided by the slicer are sufficient. However, molecular models often include overhangs, thin connections, and complex internal geometries, which require additional supports and reinforced perimeters to ensure structural stability. For this reason, the default &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; may not yield optimal results.&lt;br /&gt;
&lt;br /&gt;
Validated printing profiles for the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool are available for several printer models. These profiles provide optimized settings that produce sturdy models, reduce material consumption, and shorten print time, ensuring consistent and reliable results. Three distinct profiles are supplied, corresponding to major molecular representations: &#039;&#039;&#039;balls and sticks&#039;&#039;&#039;, &#039;&#039;&#039;surface&#039;&#039;&#039;, and &#039;&#039;&#039;cartoon&#039;&#039;&#039;. The &#039;&#039;&#039;cartoon&#039;&#039;&#039; profile is also suitable for &#039;&#039;&#039;backbone&#039;&#039;&#039;, &#039;&#039;&#039;trace&#039;&#039;&#039;, and &#039;&#039;&#039;ribbon&#039;&#039;&#039; representations. For some printers, each profile is supplied in two variants, one using standard supports and one using tree or organic supports. In the case of multi-material printers, profiles for printing with soluble support and soluble interface are also provided.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer brand and model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Profiles provided as / Slicer&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer Type, nozle size and multi-material support&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |GitHub with profiles&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to import profiles into Slicer&lt;br /&gt;
|-&lt;br /&gt;
|Original Prusa Core One&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer ]&lt;br /&gt;
|FDM / 0.4 mm / yes, 5 colors, if MMU3 installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/Prusa%20CoreOne CoreOne]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab A1Mini&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, 4 colors if AMS Lite is installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/BambuLab%20A1Mini AiMini]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab X1 Carbon&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, up to 16 colors if multiple AMS are installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ca92e7de9c72505c1b9b09e912ad177341cabc9a/BambuLab%20X1C X1Carbon]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|- &lt;br /&gt;
|Original Prusa MK3S+&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/7a7ee68d1e19f063600f53def49a99dfefbc595d/Prusa%20MK3S%2B MK3S+]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 5 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/a653c7cc6b3dec86b90117cc450d1883cc4a80bd/Ender-5-Pro Ender5Pro]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 3 v2 with a ENDERIDEX kit&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / yes, IDEX, two filaments&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/c2c74f1261a42c160e7e3898a407f21465de2ca7/Ender3-IDEX Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Kingroon KPS3 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ea733b2d05020b99f91c92f71a039c5ba8e54108/Kingroon-KPS3-Pro Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Elegoo Mars 5 Ultra&lt;br /&gt;
|no profile needed, just be sure to add supports / [https://www.elegoo.com/pages/satellite-3d-slicer?srsltid=AfmBOopMQGHgHycHMFOZALzOIC8z7bVlSHjL_jj2ShYR4QkowYKmKzUx ELEGOO SatelLite]&lt;br /&gt;
|resin / - / no&lt;br /&gt;
|&lt;br /&gt;
|no profile needed, default settings worked, just be sure to add supports. EVO supports worked well enough.  Post-processing steps: 1)washing: at least 10 min. 2) support removal 3)curring: at least 10 min on a Elegoo Mercury Plus V3.0&lt;br /&gt;
|- &lt;br /&gt;
|} &lt;br /&gt;
&#039;&#039;&#039;Notes&#039;&#039;&#039;: &lt;br /&gt;
* These profiles were developed and validated with the support of EDUMOL3D, Project [http://cercetare.bio.uaic.ro/grupuri/bioactive/content/grants/PED2024_mm.html PN-IV-P7-7.1-PED-2024-0343] financed by the Ministry of Research, Innovation and Digitization, [https://uefiscdi.gov.ro/ UEFISCDI], Romania.&lt;br /&gt;
* The profiles are a work in progress. Please check GitHub for updates. If you have suggestions for improvements, please drop a message at marius.mihasan(@)uaic.ro&lt;br /&gt;
&lt;br /&gt;
==== &#039;&#039;&#039;Note on multi-color printing &#039;&#039;&#039; ====&lt;br /&gt;
To our knowledge, only &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039; and &#039;&#039;&#039;Orca Slicer&#039;&#039;&#039; can automatically import color information from the &#039;&#039;&#039;.MTL&#039;&#039;&#039; file associated with the printable &#039;&#039;&#039;.OBJ&#039;&#039;&#039; generated by the Proteopedia &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool.  &lt;br /&gt;
At present, &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; does not support importing &#039;&#039;&#039;.MTL&#039;&#039;&#039; files directly.&lt;br /&gt;
&lt;br /&gt;
A practical workaround for &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; users is as follows:  &lt;br /&gt;
# Open the &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file in &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039;.  &lt;br /&gt;
#Verify or adjust the color mapping as needed.  &lt;br /&gt;
#Export the model as a generic &#039;&#039;&#039;.3MF&#039;&#039;&#039; file using the menu command:  &#039;&#039;File&#039;&#039; → &#039;&#039;Export&#039;&#039; → &#039;&#039;Export Generic 3MF...&#039;&#039;  &lt;br /&gt;
#Open the exported &#039;&#039;&#039;.3MF&#039;&#039;&#039; file in &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;. The color data will now be available under the &#039;&#039;&#039;Multimaterial Painting&#039;&#039;&#039; tool.&lt;br /&gt;
&lt;br /&gt;
This workflow preserves the original coloring assigned in Proteopedia and allows successful multi-color or multi-material printing on any capable 3D printer compatible with &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Other relevant resources ==&lt;br /&gt;
[Print3D_models_gallery] - examples of 3D printed molecular models from Proteopedia users.&lt;br /&gt;
&lt;br /&gt;
[https://3d.nih.gov/ NIH 3D Print Exchange] - an open, community-driven portal to download, share, and create bioscientific and medical 3D models, including for 3D printing.&lt;br /&gt;
  &lt;br /&gt;
[https://github.com/mariusmihasan/3DP-Jmol 3DP-Jmol] - the Jmol/JSmol behind the Print3D tool. Automatically generates 3D printable molecular models from structural data and can be easily integrated into web pages.&lt;br /&gt;
&lt;br /&gt;
[https://pdb101.rcsb.org/learn/3d-printing/pdb-structures-and-3d-printing 3D Printing on PDB101] - a quick guide on 3D printing molecular models and a small curated 3D models for education&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;If you print a model from Proteopedia, please share photos and feedback — let’s 3D print the whole Proteopedia!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386102</id>
		<title>Print3D help</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386102"/>
		<updated>2025-10-27T09:58:53Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== Proteopedia and 3D Printing ==&lt;br /&gt;
&lt;br /&gt;
Physical molecular models, by engaging both visual and tactile senses, provide an effective means of deepening the understanding of complex concepts in molecular biology and biochemistry. They allow students to perceive the three-dimensional organization of macromolecules, thereby enhancing comprehension of the relationship between structure and function &amp;lt;ref&amp;gt;PMID: 32590880&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 40214166&amp;lt;/ref&amp;gt;. Numerous studies have demonstrated that the use of tangible models in science education improves learning outcomes, fosters conceptual reasoning, and increases student engagement &amp;lt;ref&amp;gt;PMID: 27366318&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 26712513&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;Larsson, C., Tibell, L.A.E. Challenging Students’ Intuitions—the Influence of a Tangible Model of Virus Assembly on Students’ Conceptual Reasoning About the Process of Self-Assembly. Res Sci Educ 45, 663–690 (2015). [http://dx.doi.org/10.1007/s11165-014-9446-6 DOI: 110.1007/s11165-014-9446-6]&amp;lt;/ref&amp;gt;. The rapid development of 3D-printing technologies has made it possible to create customized and affordable molecular models  &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot;&amp;gt;PMID: 28362403&amp;lt;/ref&amp;gt; &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot;&amp;gt;PMID: 33755300&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 33384761&amp;lt;/ref&amp;gt;. &lt;br /&gt;
&lt;br /&gt;
Affordable desktop 3D printers can now be used to fabricate physical models from virtually any structure or scene on [[Proteopedia]]. This page provides an introduction to 3D printing, a step-by-step guide to generating printable files directly from [[Proteopedia]], and several tested printing profiles for common printers (e.g., Prusa Research, Bambu Lab, Creality, or Elegoo).&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== «3D Printing 101»: an introduction to 3D printing ==&lt;br /&gt;
3D printing, also known as &#039;&#039;additive manufacturing&#039;&#039;, builds physical objects layer by layer from digital designs. For more technical details please head for the excellent introductory article on [https://all3dp.com/2/what-is-3d-printing/ All3DP].  In structural biology education, 3D printing provides an affordable and accessible way to transform atomic coordinate data (e.g., from PDB, MOL or SDF files) into tangible molecular models that can be observed, handled, and discussed in class or laboratory settings.&lt;br /&gt;
&lt;br /&gt;
=== Printer Types: FDM vs. SLA/DLP ===&lt;br /&gt;
The two most accessible 3D-printing technologies that can be used to create molecular models are:&lt;br /&gt;
* &#039;&#039;&#039;FDM (Fused Deposition Modeling)&#039;&#039;&#039;&lt;br /&gt;
This method extrudes a heated thermoplastic filament (such as PLA, PETG or TPU) through a fine nozzle, depositing successive layers that form the model. FDM printers have the advantages of low cost, easy maintenance, wide availability, and being capable of printing large and colorful molecular models. This technology has a few limitations, such as: visible layer lines, lower surface resolution, and less suited for very small or intricate molecular details.&lt;br /&gt;
* &#039;&#039;&#039;SLA/DLP (Resin Printing)&#039;&#039;&#039;&lt;br /&gt;
This technique uses liquid photopolymer resin, cured layer by layer with ultraviolet light. SLA/DLP printers have the advantages of a very high resolution, smooth surfaces and are ideal for compact and detailed models (e.g., small proteins rendered as surface, ligands, or symmetric assemblies). This technology has its own limitations, such as higher material cost, post-processing requirements (washing and UV-curing), and the need for careful handling of resin.&lt;br /&gt;
&lt;br /&gt;
When choosing between FDM and SLA printers, model size and resolution are the key criteria: &#039;&#039;&#039;FDM&#039;&#039;&#039; is preferred for &#039;&#039;large, educational display models&#039;&#039;; &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; is optimal for &#039;&#039;small, precise structures&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
While FDM and SLA/DLP are the most widely used technologies in educational and research contexts due to their accessibility, other additive manufacturing methods also exist —such as &#039;&#039;Selective Laser Sintering&#039;&#039; (SLS), &#039;&#039;PolyJet&#039;&#039;, and &#039;&#039;Binder Jetting&#039;&#039;— each employing different materials and curing mechanisms. These industrial-grade techniques can produce highly detailed or multi-material parts but are generally more expensive and less accessible for classroom use. For an overview of major 3D-printing technologies, see [https://all3dp.com/1/types-of-3d-printers-3d-printing-technology/ All3DP: Complete Overview of the Types of 3D Printers]&lt;br /&gt;
&lt;br /&gt;
=== Single- vs. Multi-Material Printers ===&lt;br /&gt;
Most entry-level desktop 3D printers use a single filament or resin, producing models in one color or material. However, multi-material systems (such as [https://eu.store.bambulab.com/products/ams-multicolor-printing?from=home_web_top_navigation Bambu Lab AMS] and its variants or [https://www.prusa3d.com/category/original-prusa-mmu3/ Prusa MMU3]) can simultaneously print multiple filaments, enabling color-coded domains, subunits, or ligands directly in one print. For complex color information, users can also apply post-print color coding (painting or labeling) or print separate parts and assemble them manually.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A large FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A multi-material FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Small resin-printed models&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:GABAA_receptor.png|320px|center|thumb| GABAA receptor, [[6x3x]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Bacterial_Ribosome_multimaterial_FDM.png|348px|center|thumb| Bacterial 70S ribosome, [[4v5d]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Dna_insuline_sla.png|252px|center|thumb|DNA (left) and insulin (right) models, [[4bna]] and [[4ins]], scale at the bottom in cm]]&lt;br /&gt;
|-&lt;br /&gt;
|Trace Model of the GABAA receptor printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com] &lt;br /&gt;
|Surface model of the Bacterial 70S ribosome printed on a multi-material capable printer (BambuLab X1C AMS). Blue and violet are ribosomal proteins, orange and yellow are rRNAs, and black is tRNA. Printable files available on [https://www.printables.com/model/1430877-bacterial-70s-ribosome Printables.com]&lt;br /&gt;
|Balls and sticks and cartoon models of DNA (right) and insulin (left)&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== File Formats Used in 3D Printing ===&lt;br /&gt;
Proteopedia supports two export formats for generating printable molecular models:&lt;br /&gt;
*&#039;&#039;&#039;.STL&#039;&#039;&#039; (Stereolithography): the most common and universally compatible format; encodes only surface geometry, without color or texture information.&lt;br /&gt;
*&#039;&#039;&#039;.OBJ&#039;&#039;&#039; (Wavefront Object) with an associated &#039;&#039;&#039;.MTL&#039;&#039;&#039; (Material Template Library) files: includes both geometry and optional color/texture data; useful for color prints.&lt;br /&gt;
&lt;br /&gt;
Another widely adopted file format used in 3D printing is the &#039;&#039;&#039;.3MF&#039;&#039;&#039; (3D Manufacturing Format): a modern open standard that stores geometry, color, and multi-material metadata in a single file—recommended for advanced printers. For a more extensive pros and cons of different 3D printing file formats please see [https://all3dp.com/2/3d-file-format-3d-model-types/ The Main 3D Printing File Formats on all3dp]. &lt;br /&gt;
&lt;br /&gt;
STL is ideal for single-color models and maximum compatibility, while OBJ/MTL is recommended for multi-material workflows. 3MF files will be used in this tutorial to save the model and printing settings. &lt;br /&gt;
&lt;br /&gt;
Support in Proteopedia for these formats is based on the export capabilities of Jmol/JSmol; for details, see [http://wiki.jmol.org/index.php/File_formats/3D_Objects#STL STL] and [http://wiki.jmol.org/index.php/File_formats/3D_Objects#OBJ OBJ]&lt;br /&gt;
&lt;br /&gt;
== Overview of the 3D printing process ==&lt;br /&gt;
3D printing enables the transformation of atomic-level structural data into tangible macromolecular models that can be explored through both sight and touch.  &lt;br /&gt;
The process generally follows several main steps, each requiring specific types of software and hardware.&lt;br /&gt;
[[Image:3D_printing_workflow_v2.png|thumb|left|400px|Overview of the 3D printing workflow for generating physical molecular models.]]&lt;br /&gt;
	&lt;br /&gt;
=== Preparing the structure and generating a printable File ===&lt;br /&gt;
:The first stage involves creating a printable three-dimensional representation of the molecule. Some molecular-graphics programs such as [https://www.pymol.org/ PyMOL], [https://www.rbvi.ucsf.edu/chimerax/ UCSF ChimeraX], [https://molstar.org/Mol*], or [https://jmol.sourceforge.net/ Jmol] can be used not only to visualize a structure (from the Protein Data Bank or other sources), but also to export the resulting geometry in a .STL or .OBJ format. However, the default visualization styles of these programs are &#039;&#039;&#039;&#039;&#039;not directly suitable for 3D printing&#039;&#039;&#039;&#039;&#039;. Therefore, when preparing a model for fabrication, it is important to:&lt;br /&gt;
:* &#039;&#039;&#039;Select an appropriate molecular representation&#039;&#039;&#039; (e.g., surface, cartoon, sticks, spheres) depending on the pedagogical or structural feature you wish to highlight.  &lt;br /&gt;
:* &#039;&#039;&#039;Add struts or connectors&#039;&#039;&#039; to increase the mechanical stability of the model, especially for large complexes or long helices.  &lt;br /&gt;
:* &#039;&#039;&#039;Remove specific struts or pseudobonds&#039;&#039;&#039; when individual components — ligands, subunits, or cofactors — need to remain detachable.  &lt;br /&gt;
:* &#039;&#039;&#039;Adjust thickness&#039;&#039;&#039; of atoms, bonds, helices, and sheets to ensure adequate rigidity and printability (features thinner than the printer’s nozzle diameter or resin resolution may break).  &lt;br /&gt;
:* &#039;&#039;&#039;Apply meaningful coloring&#039;&#039;&#039; when preparing multi-material prints, for instance, to distinguish domains, chains, ligands or atoms.&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene that automates the process and enables users to effortlessly generate 3D-printable molecular models - more on that in the corresponding section [[#Generating printable files on Proteopedia|Generating printable files on Proteopedia]] within this page. For advanced users wanting to do this manually, we highly recommend two guides: &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot; /&amp;gt; and &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
=== Slicing the Model ===&lt;br /&gt;
Before printing, the STL file must be processed by a &#039;&#039;&#039;slicer&#039;&#039;&#039; — specialized software that converts 3D geometry into a series of horizontal layers. The slicer also generates &#039;&#039;&#039;G-code&#039;&#039;&#039;, the set of instructions that control the printer. These commands are printer-specific and include parameters such as extrusion speed, layer thickness, temperature, and movement. Together, they are usually stored as a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;.  &lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an FDM printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;number of perimeters&#039;&#039;&#039;, which affects mechanical strength and print time;&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines resolution and print duration;&lt;br /&gt;
:* &#039;&#039;&#039;infill density&#039;&#039;&#039;, which determines internal strength and affects print time;&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, temporary structures that hold overhanging regions;&lt;br /&gt;
:* &#039;&#039;&#039;print orientation&#039;&#039;&#039;, which influences surface quality, mechanical strength, and the amount of supports required.&lt;br /&gt;
:All these parameters make up a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. In this step, users must also select the material-specific parameters, or apply a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. More details on these profiles are provided later on this page.&lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines vertical resolution and print time; thinner layers produce smoother surfaces but significantly increase printing duration.&lt;br /&gt;
:* &#039;&#039;&#039;exposure time&#039;&#039;&#039;, which controls how long each layer is cured by UV light; optimal exposure ensures proper adhesion between layers without over-curing fine details.&lt;br /&gt;
:* &#039;&#039;&#039;bottom-layer exposure and count&#039;&#039;&#039;, which influence model adhesion to the build platform — longer exposures and additional base layers improve stability during printing.&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, which anchor the model to the build plate and prevent deformation during peeling; proper placement reduces surface marks and print failures.&lt;br /&gt;
:* &#039;&#039;&#039;model orientation&#039;&#039;&#039;, which affects surface quality, support contact area, and resin drainage; angling the model (typically 30–45°) minimizes suction forces and improves print reliability.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for FDM printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for resin printing&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:Insuline_sliced_prusa.gif|386px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|[[Image:Insuline_Sliced_SLA.gif|372px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|-&lt;br /&gt;
|Cartoon model of insulin sliced in PrusaSlicer and ready to be printed on FDM printers. The arrow shows the trajectory of the print head on a single slice or layer. Orange is the model, green are the supports. &lt;br /&gt;
|Cartoon model of insulin sliced in Elegoo SatelLite and ready to be printed on FDM printer.On the left, with blue is the model, with gray are the supports. On the right is the image on the UV screen. &lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== 3D Printing the Model ===&lt;br /&gt;
:The prepared G-code is then transferred to the 3D printer, either via an SD card, USB flash drive, or Wi-Fi connection. During printing, close observation of the first few layers is essential to ensure good adhesion to the build plate and a successful print. Total printing time depends on model size, selected layer height, and printer speed. &#039;&#039;Small peptide&#039;&#039; models may print in &#039;&#039;&#039;less than an hour&#039;&#039;&#039;, whereas l&#039;&#039;arge multimeric assemblies&#039;&#039; can require &#039;&#039;&#039;several hours or days&#039;&#039;&#039;. &#039;&#039;Multi-color&#039;&#039; or &#039;&#039;multi-material&#039;&#039; prints generally take &#039;&#039;&#039;longer&#039;&#039;&#039;, while &#039;&#039;SLA/DLP&#039;&#039; printers are generally &#039;&#039;&#039;faster&#039;&#039;&#039; due to their simultaneous layer exposure.&lt;br /&gt;
=== Post-Processing ===&lt;br /&gt;
:After printing, the model undergoes post-processing, which varies depending on the printing technology used:&lt;br /&gt;
:* For &#039;&#039;&#039;FDM prints&#039;&#039;&#039;, supports are removed mechanically, and surfaces can be smoothed by light sanding or polishing.&lt;br /&gt;
:* For &#039;&#039;&#039;resin prints&#039;&#039;&#039;, supports are removed mechanically, parts are washed in isopropanol to remove uncured resin and then exposed to UV light for final curing.&lt;br /&gt;
:Models printed in multiple parts can be assembled using cyanoacrylate or epoxy adhesive. Optional finishing steps (painting, labeling) can improve contrast between subunits or highlight functional regions.&lt;br /&gt;
&lt;br /&gt;
==Generating printable files on Proteopedia==&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene, enabling logged users to effortlessly generate 3D-printable molecular models directly from its pages. The tool is powered by [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;], a script that analyzes the structural data and automatically scales the model’s geometry to match the printable volume of a medium-size desktop 3D printer (e.g., Ender-3, 210×210×210 mm). During this process, the tool evaluates the molecular bounding box, atom radii, and bond lengths, then proportionally adjusts all dimensions to achieve a realistic and mechanically robust print scale — preserving scientific accuracy while ensuring manufacturability. For advanced users, [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;] may also be used in conjunction with the [https://jmol.sourceforge.net/ &#039;&#039;&#039;Jmol&#039;&#039;&#039;] program, providing full access to its scripting capabilities and advanced export features.&lt;br /&gt;
==Step-by-step guide for automatic generation of printable files on Proteopedia==&lt;br /&gt;
=== Open a structure and access the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool ===&lt;br /&gt;
Log in with your Proteopedia Username and password. Navigate to any Proteopedia page (for example, [[Introduction_to_protein_structure]]). The corresponding 3D structure will load in the viewer on the right.  &lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_button_in_Proteopedia.png|thumb|left|400px|The &#039;&#039;&#039;Print3D&#039;&#039;&#039; button on a Proteopedia page]]&lt;br /&gt;
&lt;br /&gt;
At the bottom of the structure display window, locate and click the &#039;&#039;&#039;Print3D&#039;&#039;&#039; button. The tool will launch and begin analyzing the current molecular structure.  &lt;br /&gt;
This process may take some time to complete, depending on the size of the structure.  &lt;br /&gt;
Please wait until the message &#039;&#039;&#039;Analyzing structure...&#039;&#039;&#039; disappears and the next page is displayed — this marks the start of the two-step printing workflow.&lt;br /&gt;
=== Select a molecular representation and a printing scale ===&lt;br /&gt;
In this new page, some user input is required. Each option includes a short explanation; the key steps are outlined below, but feel free to explore and adopt the settings that best fit your use case.&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step1.png|thumb|left|400px|Selecting molecular representation and printing scale]]&lt;br /&gt;
&lt;br /&gt;
(1) &#039;&#039;&#039;Choose a molecular representation&#039;&#039;&#039; from the &#039;&#039;&#039;Scheme&#039;&#039;&#039; list, based on your goal:&lt;br /&gt;
* &#039;&#039;&#039;Backbone&#039;&#039;&#039;, &#039;&#039;&#039;Trace&#039;&#039;&#039;, or &#039;&#039;&#039;Ribbon&#039;&#039;&#039; — to emphasize secondary structure (effective for teaching protein folds).&lt;br /&gt;
* &#039;&#039;&#039;Surface&#039;&#039;&#039; — to highlight molecular topology and binding sites.&lt;br /&gt;
* &#039;&#039;&#039;Ball &amp;amp; Stick&#039;&#039;&#039; — atom-level detail for ligands or small molecules; usually impractical for large proteins or complexes.&lt;br /&gt;
* &#039;&#039;&#039;Proteopedia Scene&#039;&#039;&#039; — attempts to render the current page’s scene directly; may not work for all scenes. This is not fully implemented and only available for a few users.&lt;br /&gt;
&#039;&#039;Note:&#039;&#039; Some representations may be unavailable for a given structure because they are not printable in a reliable way.&lt;br /&gt;
&lt;br /&gt;
(2) In the &#039;&#039;&#039;Printer&#039;&#039;&#039; section, select whether you want a &#039;&#039;&#039;single-color&#039;&#039;&#039; or a &#039;&#039;&#039;multi-color&#039;&#039;&#039; print.&lt;br /&gt;
&lt;br /&gt;
(3) In the &#039;&#039;&#039;Printer scale&#039;&#039;&#039; section, set the desired size of the printed model. The tool constrains safe sizes based on the chosen representation and displays the physical dimensions (mm). &#039;&#039;&#039;Important! Please note the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;printer scale value in %&amp;lt;/span&amp;gt; as it is going to be required downstream in the next section of this workflow, [[#Printing files from Proteopedia|Printing files from Proteopedia]]&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
(4) When ready, click the green &#039;&#039;&#039;Make printer files&#039;&#039;&#039; button. Please wait patiently until the  &#039;&#039;Generating files for 3D printing of...&#039;&#039; message disappears and the final step is displayed.&lt;br /&gt;
&lt;br /&gt;
===Download the .STL or .OBJ files===&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step2.png|thumb|left|400px|Final step in generating printable files]]&lt;br /&gt;
&lt;br /&gt;
In this final page, a 3D preview of the generated model is displayed.&lt;br /&gt;
You can use the mouse to rotate, zoom, and inspect the model from different angles. If the result meets your needs, click the green (A) &#039;&#039;&#039;Download files&#039;&#039;&#039; button and save the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive containing the &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; files on your computer. If your model needs further improvements, hit the green (B) &#039;&#039;&#039;Same structure&#039;&#039;&#039; button to return to the previous screen and adjust your settings.&lt;br /&gt;
&lt;br /&gt;
 maybe a movie is better- need to decide ?&lt;br /&gt;
&lt;br /&gt;
{{clear}}&lt;br /&gt;
== Printing files from Proteopedia ==&lt;br /&gt;
Unzipping the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive will produce the exported &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file, along with an optional &#039;&#039;&#039;.MTL&#039;&#039;&#039; material file. &lt;br /&gt;
=== Using 3D printing services ===&lt;br /&gt;
If you do not have a 3D printer, you can still obtain physical models by using locally available 3D-printing services. Just search on [https://www.google.com/maps Google Maps] with the term  &#039;&#039;&#039;3D printing&#039;&#039;&#039; in your area. Here is short list of well-known 3D Printing service providers that may also ship worldwide: &lt;br /&gt;
&lt;br /&gt;
* [https://www.shapeways.com/ &#039;&#039;&#039;Shapeways&#039;&#039;&#039;] — global service offering a wide range of materials and colors. Educational discounts are available through their academic program.&lt;br /&gt;
* [https://www.sculpteo.com/en/ &#039;&#039;&#039;Sculpteo&#039;&#039;&#039;] — Europe-based provider offering fast turnaround and many printing technologies, including resin and polymer options.&lt;br /&gt;
* [https://www.xometry.com/capabilities/3d-printing-service &#039;&#039;&#039;Xometry&#039;&#039;&#039;] — large international network providing access to industrial-grade printing methods such as FDM, SLA, SLS, and DMLS.&lt;br /&gt;
* [https://craftcloud3d.com/ &#039;&#039;&#039;Craftcloud&#039;&#039;&#039;] — an aggregator that compares multiple providers and finds the best price and lead time for your uploaded model.&lt;br /&gt;
&lt;br /&gt;
When contacting a printing service, provide the exported files together with the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value in %&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ([[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). It is also advisable to share the link to this Proteopedia page so that the operator understands the peculiarities of printing molecular models. &lt;br /&gt;
&lt;br /&gt;
=== Using a desktop 3D printer ===&lt;br /&gt;
&lt;br /&gt;
Before importing the .STL or .OBJ file into your slicer software, it is recommended to inspect and, if necessary, repair the model to ensure printability. Common issues include non-manifold geometry, intersecting faces, and missing surfaces.  The example below demonstrates how to use [https://www.blender.org/ &#039;&#039;&#039;Blender&#039;&#039;&#039;] together with its [https://extensions.blender.org/add-ons/print3d-toolbox/ &#039;&#039;&#039;3D Print Toolbox extension&#039;&#039;&#039;] to improve the printability of the .STL and .OBJ files generated with the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in [[Proteopedia]]. &#039;&#039;&#039;Important note&#039;&#039;&#039;: The repair process is largely automated but may introduce artifacts. Carefully inspect the corrected model for any missing or distorted sections, atoms, or bonds, and determine whether these omissions affect the intended purpose of the printed model.  &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for single color or resin printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for multi-color FDM printing&lt;br /&gt;
|-&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=k6u-5JnoP-c&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=OCisrIZMIDM&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|}  &lt;br /&gt;
&lt;br /&gt;
Once the repaired &#039;&#039;&#039;.STL or .OBJ&#039;&#039;&#039; file is ready, it can be imported into your slicer software. In this step, you will prepare the file for printing by applying appropriate printer, filament, and print-settings profiles.&lt;br /&gt;
&lt;br /&gt;
*Apply the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value (%)&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ( [[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). This step ensures that the model fits your print bed and maintains structural integrity during printing. The location of the scale (%) input field varies depending on the slicer software you are using.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Orient the model on the print bed&#039;&#039;&#039; so that its largest, flattest surface rests on the bed. This minimizes the need for supports and improves adhesion. If your slicer includes an Auto Orient or Auto Arrange function, use it to optimize placement. (&#039;&#039;Hint&#039;&#039;: Bambu Studio and Orca Slicer include this feature, Ultimaker Cura has a [https://marketplace.ultimaker.com/app/cura/plugins/nallath/OrientationPlugin Auto-Orientation plugin] available, while PrusaSlicer currently does not.)&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Select the printer&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that matches your device.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Choose the material&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; corresponding to the filament type (e.g., PLA, PETG, TPU) and manufacturer you intend to use.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Adjust the printing parameters&#039;&#039;&#039; by selecting a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that defines layer height, infill, speed, and support options.&lt;br /&gt;
&lt;br /&gt;
In most cases, the default &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; and &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; provided by the slicer are sufficient. However, molecular models often include overhangs, thin connections, and complex internal geometries, which require additional supports and reinforced perimeters to ensure structural stability. For this reason, the default &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; may not yield optimal results.&lt;br /&gt;
&lt;br /&gt;
Validated printing profiles for the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool are available for several printer models. These profiles provide optimized settings that produce sturdy models, reduce material consumption, and shorten print time, ensuring consistent and reliable results. Three distinct profiles are supplied, corresponding to major molecular representations: &#039;&#039;&#039;balls and sticks&#039;&#039;&#039;, &#039;&#039;&#039;surface&#039;&#039;&#039;, and &#039;&#039;&#039;cartoon&#039;&#039;&#039;. The &#039;&#039;&#039;cartoon&#039;&#039;&#039; profile is also suitable for &#039;&#039;&#039;backbone&#039;&#039;&#039;, &#039;&#039;&#039;trace&#039;&#039;&#039;, and &#039;&#039;&#039;ribbon&#039;&#039;&#039; representations. For some printers, each profile is supplied in two variants, one using standard supports and one using tree or organic supports. In the case of multi-material printers, profiles for printing with soluble support and soluble interface are also provided.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer brand and model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Profiles provided as / Slicer&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer Type, nozle size and multi-material support&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |GitHub with profiles&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to import profiles into Slicer&lt;br /&gt;
|-&lt;br /&gt;
|Original Prusa Core One&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer ]&lt;br /&gt;
|FDM / 0.4 mm / yes, 5 colors, if MMU3 installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/Prusa%20CoreOne CoreOne]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab A1Mini&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, 4 colors if AMS Lite is installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/BambuLab%20A1Mini AiMini]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab X1 Carbon&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, up to 16 colors if multiple AMS are installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ca92e7de9c72505c1b9b09e912ad177341cabc9a/BambuLab%20X1C X1Carbon]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|- &lt;br /&gt;
|Original Prusa MK3S+&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/7a7ee68d1e19f063600f53def49a99dfefbc595d/Prusa%20MK3S%2B MK3S+]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 5 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/a653c7cc6b3dec86b90117cc450d1883cc4a80bd/Ender-5-Pro Ender5Pro]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 3 v2 with a ENDERIDEX kit&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / yes, IDEX, two filaments&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/c2c74f1261a42c160e7e3898a407f21465de2ca7/Ender3-IDEX Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Kingroon KPS3 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ea733b2d05020b99f91c92f71a039c5ba8e54108/Kingroon-KPS3-Pro Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Elegoo Mars 5 Ultra&lt;br /&gt;
|no profile needed, just be sure to add supports / [https://www.elegoo.com/pages/satellite-3d-slicer?srsltid=AfmBOopMQGHgHycHMFOZALzOIC8z7bVlSHjL_jj2ShYR4QkowYKmKzUx ELEGOO SatelLite]&lt;br /&gt;
|resin / - / no&lt;br /&gt;
|&lt;br /&gt;
|no profile needed, default settings worked, just be sure to add supports. EVO supports worked well enough.  Post-processing steps: 1)washing: at least 10 min. 2) support removal 3)curring: at least 10 min on a Elegoo Mercury Plus V3.0&lt;br /&gt;
|- &lt;br /&gt;
|} &lt;br /&gt;
&#039;&#039;&#039;Notes&#039;&#039;&#039;: &lt;br /&gt;
* These profiles were developed and validated with the support of EDUMOL3D, Project [http://cercetare.bio.uaic.ro/grupuri/bioactive/content/grants/PED2024_mm.html PN-IV-P7-7.1-PED-2024-0343] financed by the Ministry of Research, Innovation and Digitization, [https://uefiscdi.gov.ro/ UEFISCDI], Romania.&lt;br /&gt;
* The profiles are a work in progress. Please check GitHub for updates. If you have suggestions for improvements, please drop a message at marius.mihasan(@)uaic.ro&lt;br /&gt;
&lt;br /&gt;
==== &#039;&#039;&#039;Note on multi-color printing &#039;&#039;&#039; ====&lt;br /&gt;
To our knowledge, only &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039; and &#039;&#039;&#039;Orca Slicer&#039;&#039;&#039; can automatically import color information from the &#039;&#039;&#039;.MTL&#039;&#039;&#039; file associated with the printable &#039;&#039;&#039;.OBJ&#039;&#039;&#039; generated by the Proteopedia &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool.  &lt;br /&gt;
At present, &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; does not support importing &#039;&#039;&#039;.MTL&#039;&#039;&#039; files directly.&lt;br /&gt;
&lt;br /&gt;
A practical workaround for &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; users is as follows:  &lt;br /&gt;
# Open the &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file in &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039;.  &lt;br /&gt;
#Verify or adjust the color mapping as needed.  &lt;br /&gt;
#Export the model as a generic &#039;&#039;&#039;.3MF&#039;&#039;&#039; file using the menu command:  &#039;&#039;File&#039;&#039; → &#039;&#039;Export&#039;&#039; → &#039;&#039;Export Generic 3MF...&#039;&#039;  &lt;br /&gt;
#Open the exported &#039;&#039;&#039;.3MF&#039;&#039;&#039; file in &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;. The color data will now be available under the &#039;&#039;&#039;Multimaterial Painting&#039;&#039;&#039; tool.&lt;br /&gt;
&lt;br /&gt;
This workflow preserves the original coloring assigned in Proteopedia and allows successful multi-color or multi-material printing on any capable 3D printer compatible with &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Other relevant resources ==&lt;br /&gt;
[Print3D_models_gallery Proteopedia gallery of 3D printed models] - examples of 3D printed molecular models from Proteopedia users.&lt;br /&gt;
&lt;br /&gt;
[https://3d.nih.gov/ NIH 3D Print Exchange] - an open, community-driven portal to download, share, and create bioscientific and medical 3D models, including for 3D printing.&lt;br /&gt;
  &lt;br /&gt;
[https://github.com/mariusmihasan/3DP-Jmol 3DP-Jmol] - the Jmol/JSmol behind the Print3D tool. Automatically generates 3D printable molecular models from structural data and can be easily integrated into web pages.&lt;br /&gt;
&lt;br /&gt;
[https://pdb101.rcsb.org/learn/3d-printing/pdb-structures-and-3d-printing 3D Printing on PDB101] - a quick guide on 3D printing molecular models and a small curated 3D models for education&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;If you print a model from Proteopedia, please share photos and feedback — let’s 3D print the whole Proteopedia!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Print3D_models_gallery&amp;diff=4386100</id>
		<title>Print3D models gallery</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_models_gallery&amp;diff=4386100"/>
		<updated>2025-10-27T09:41:12Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Welcome to the Proteopedia gallery of 3D printed models==&lt;br /&gt;
&lt;br /&gt;
Did you use the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in Proteopedia to create a printable model? &lt;br /&gt;
&lt;br /&gt;
Do you have pictures of the final 3D printed model of a molecule? &lt;br /&gt;
&lt;br /&gt;
Or better, do you have a picture of the model put to good use? &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;We would love to know more about it&#039;&#039;&#039;. Please feel free to contribute to this page and share your prints!  Note: If editing this page it&#039;s not for you and you would prefer to focus on 3D printing, drop us an e-mail at marius.mihasan(@)uaic.ro and we would love to hear your story and share it on this page. &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Picture&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Details (including link to Proteopedia page if possible)&lt;br /&gt;
|-&lt;br /&gt;
| A simplified model of SV40 Capsid&lt;br /&gt;
|[[Image:SV40_Capsid_3DPrinted.jpg|400px|center|thumb| SV40 Capsid, [[SV40_Capsid_Simplified]]]]&lt;br /&gt;
|Model of SV40 Capsid printed on multi-material printer (Bambulab A1 Mini). Printable files available on [https://www.printables.com/model/1308340-a-simplified-model-of-sv40-capsid Printables.com]. Generated with the Proteopedia Print3D tool from [[SV40_Capsid_Simplified]]. Printed by [[User:Marius Mihasan|Marius Mihasan]] 12:27, 8 October 2025 (UTC).&lt;br /&gt;
|-&lt;br /&gt;
| GABBA receptor&lt;br /&gt;
|[[Image:GABAA_receptor.png|400px|center|thumb| GABAA receptor, [[6x3x]]]]&lt;br /&gt;
|Trace Model of the GABAA receptor [[6x3x]] printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com]. Printed by [[User:Marius Mihasan|Marius Mihasan]] 12:27, 8 October 2025 (UTC)&lt;br /&gt;
|-&lt;br /&gt;
|Model 3  &lt;br /&gt;
|Image with model 3&lt;br /&gt;
|Description of model 3&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Print3D_models_gallery&amp;diff=4386098</id>
		<title>Print3D models gallery</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_models_gallery&amp;diff=4386098"/>
		<updated>2025-10-27T09:39:31Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: New page: ==Welcome to the Proteopedia gallery of 3D printed models==  Did you use the &amp;#039;&amp;#039;&amp;#039;Print3D&amp;#039;&amp;#039;&amp;#039; tool in Proteopedia to create a printable model?   Do you have pictures of the final 3D printed m...&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Welcome to the Proteopedia gallery of 3D printed models==&lt;br /&gt;
&lt;br /&gt;
Did you use the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in Proteopedia to create a printable model? &lt;br /&gt;
&lt;br /&gt;
Do you have pictures of the final 3D printed model of a molecule? &lt;br /&gt;
&lt;br /&gt;
Or better, do you have a picture of the model put to good use? &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;We would love to know more about it&#039;&#039;&#039;. Please feel free to contribute to this page and share your prints!  Note: If editing this page it&#039;s not for you and you would prefer to focus on 3D printing, drop us an e-mail at marius.mihasan(@)uaic.ro and we would love to hear your story and share it on this page. &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Picture&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Details (including link to Proteopedia page if possible)&lt;br /&gt;
|-&lt;br /&gt;
| A simplified model of SV40 Capsid&lt;br /&gt;
|[[Image:SV40_Capsid_3DPrinted.jpg|400px|center|thumb| SV40 Capsid, [[SV40_Capsid_Simplified]]]]&lt;br /&gt;
|Model of SV40 Capsid printed on multi-material printer (Bambulab A1 Mini). Printable files available on [https://www.printables.com/model/1308340-a-simplified-model-of-sv40-capsid Printables.com]. Generated with the Proteopedia Print3D tool from [[SV40_Capsid_Simplified]]. Printed by [[User:Marius Mihasan|Marius Mihasan]] 12:27, 8 October 2025 (UTC).&lt;br /&gt;
|-&lt;br /&gt;
| GABBA receptor&lt;br /&gt;
|[[Image:GABAA_receptor.png|400px|center|thumb| GABAA receptor, [[6x3x]]]]&lt;br /&gt;
|Trace Model of the GABAA receptor [[6x3x]] printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com]. Printed by [[User:Marius Mihasan|Marius Mihasan]] 12:27, 8 October 2025 (UTC)&lt;br /&gt;
|-&lt;br /&gt;
|Model 3  &lt;br /&gt;
|Image with model 3&lt;br /&gt;
|Description of model 3&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386096</id>
		<title>Print3D help</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Print3D_help&amp;diff=4386096"/>
		<updated>2025-10-27T09:25:55Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: New page: == Proteopedia and 3D Printing ==  Physical molecular models, by engaging both visual and tactile senses, provide an effective means of deepening the understanding of complex concepts in m...&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;== Proteopedia and 3D Printing ==&lt;br /&gt;
&lt;br /&gt;
Physical molecular models, by engaging both visual and tactile senses, provide an effective means of deepening the understanding of complex concepts in molecular biology and biochemistry. They allow students to perceive the three-dimensional organization of macromolecules, thereby enhancing comprehension of the relationship between structure and function &amp;lt;ref&amp;gt;PMID: 32590880&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 40214166&amp;lt;/ref&amp;gt;. Numerous studies have demonstrated that the use of tangible models in science education improves learning outcomes, fosters conceptual reasoning, and increases student engagement &amp;lt;ref&amp;gt;PMID: 27366318&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 26712513&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;Larsson, C., Tibell, L.A.E. Challenging Students’ Intuitions—the Influence of a Tangible Model of Virus Assembly on Students’ Conceptual Reasoning About the Process of Self-Assembly. Res Sci Educ 45, 663–690 (2015). [http://dx.doi.org/10.1007/s11165-014-9446-6 DOI: 110.1007/s11165-014-9446-6]&amp;lt;/ref&amp;gt;. The rapid development of 3D-printing technologies has made it possible to create customized and affordable molecular models  &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot;&amp;gt;PMID: 28362403&amp;lt;/ref&amp;gt; &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot;&amp;gt;PMID: 33755300&amp;lt;/ref&amp;gt; &amp;lt;ref&amp;gt;PMID: 33384761&amp;lt;/ref&amp;gt;. &lt;br /&gt;
&lt;br /&gt;
Affordable desktop 3D printers can now be used to fabricate physical models from virtually any structure or scene on [[Proteopedia]]. This page provides an introduction to 3D printing, a step-by-step guide to generating printable files directly from [[Proteopedia]], and several tested printing profiles for common printers (e.g., Prusa Research, Bambu Lab, Creality, or Elegoo).&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Let’s 3D-print the whole [[Proteopedia]]!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== «3D Printing 101»: an introduction to 3D printing ==&lt;br /&gt;
3D printing, also known as &#039;&#039;additive manufacturing&#039;&#039;, builds physical objects layer by layer from digital designs. For more technical details please head for the excellent introductory article on [https://all3dp.com/2/what-is-3d-printing/ All3DP].  In structural biology education, 3D printing provides an affordable and accessible way to transform atomic coordinate data (e.g., from PDB, MOL or SDF files) into tangible molecular models that can be observed, handled, and discussed in class or laboratory settings.&lt;br /&gt;
&lt;br /&gt;
=== Printer Types: FDM vs. SLA/DLP ===&lt;br /&gt;
The two most accessible 3D-printing technologies that can be used to create molecular models are:&lt;br /&gt;
* &#039;&#039;&#039;FDM (Fused Deposition Modeling)&#039;&#039;&#039;&lt;br /&gt;
This method extrudes a heated thermoplastic filament (such as PLA, PETG or TPU) through a fine nozzle, depositing successive layers that form the model. FDM printers have the advantages of low cost, easy maintenance, wide availability, and being capable of printing large and colorful molecular models. This technology has a few limitations, such as: visible layer lines, lower surface resolution, and less suited for very small or intricate molecular details.&lt;br /&gt;
* &#039;&#039;&#039;SLA/DLP (Resin Printing)&#039;&#039;&#039;&lt;br /&gt;
This technique uses liquid photopolymer resin, cured layer by layer with ultraviolet light. SLA/DLP printers have the advantages of a very high resolution, smooth surfaces and are ideal for compact and detailed models (e.g., small proteins rendered as surface, ligands, or symmetric assemblies). This technology has its own limitations, such as higher material cost, post-processing requirements (washing and UV-curing), and the need for careful handling of resin.&lt;br /&gt;
&lt;br /&gt;
When choosing between FDM and SLA printers, model size and resolution are the key criteria: &#039;&#039;&#039;FDM&#039;&#039;&#039; is preferred for &#039;&#039;large, educational display models&#039;&#039;; &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; is optimal for &#039;&#039;small, precise structures&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
While FDM and SLA/DLP are the most widely used technologies in educational and research contexts due to their accessibility, other additive manufacturing methods also exist —such as &#039;&#039;Selective Laser Sintering&#039;&#039; (SLS), &#039;&#039;PolyJet&#039;&#039;, and &#039;&#039;Binder Jetting&#039;&#039;— each employing different materials and curing mechanisms. These industrial-grade techniques can produce highly detailed or multi-material parts but are generally more expensive and less accessible for classroom use. For an overview of major 3D-printing technologies, see [https://all3dp.com/1/types-of-3d-printers-3d-printing-technology/ All3DP: Complete Overview of the Types of 3D Printers]&lt;br /&gt;
&lt;br /&gt;
=== Single- vs. Multi-Material Printers ===&lt;br /&gt;
Most entry-level desktop 3D printers use a single filament or resin, producing models in one color or material. However, multi-material systems (such as [https://eu.store.bambulab.com/products/ams-multicolor-printing?from=home_web_top_navigation Bambu Lab AMS] and its variants or [https://www.prusa3d.com/category/original-prusa-mmu3/ Prusa MMU3]) can simultaneously print multiple filaments, enabling color-coded domains, subunits, or ligands directly in one print. For complex color information, users can also apply post-print color coding (painting or labeling) or print separate parts and assemble them manually.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A large FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |A multi-material FDM-printed model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Small resin-printed models&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:GABAA_receptor.png|320px|center|thumb| GABAA receptor, [[6x3x]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Bacterial_Ribosome_multimaterial_FDM.png|348px|center|thumb| Bacterial 70S ribosome, [[4v5d]], scale at the bottom in cm]]&lt;br /&gt;
|[[Image:Dna_insuline_sla.png|252px|center|thumb|DNA (left) and insulin (right) models, [[4bna]] and [[4ins]], scale at the bottom in cm]]&lt;br /&gt;
|-&lt;br /&gt;
|Trace Model of the GABAA receptor printed on a single material FDM-Printer (Prusa MK3S+). Each of the 5 subunits was printed separately and can be assembled. Printable files available on [https://www.printables.com/model/1317843-model-of-human-gabaa-receptor-in-complex-with-gaba Printables.com] &lt;br /&gt;
|Surface model of the Bacterial 70S ribosome printed on a multi-material capable printer (BambuLab X1C AMS). Blue and violet are ribosomal proteins, orange and yellow are rRNAs, and black is tRNA. Printable files available on [https://www.printables.com/model/1430877-bacterial-70s-ribosome Printables.com]&lt;br /&gt;
|Balls and sticks and cartoon models of DNA (right) and insulin (left)&lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== File Formats Used in 3D Printing ===&lt;br /&gt;
Proteopedia supports two export formats for generating printable molecular models:&lt;br /&gt;
*&#039;&#039;&#039;.STL&#039;&#039;&#039; (Stereolithography): the most common and universally compatible format; encodes only surface geometry, without color or texture information.&lt;br /&gt;
*&#039;&#039;&#039;.OBJ&#039;&#039;&#039; (Wavefront Object) with an associated &#039;&#039;&#039;.MTL&#039;&#039;&#039; (Material Template Library) files: includes both geometry and optional color/texture data; useful for color prints.&lt;br /&gt;
&lt;br /&gt;
Another widely adopted file format used in 3D printing is the &#039;&#039;&#039;.3MF&#039;&#039;&#039; (3D Manufacturing Format): a modern open standard that stores geometry, color, and multi-material metadata in a single file—recommended for advanced printers. For a more extensive pros and cons of different 3D printing file formats please see [https://all3dp.com/2/3d-file-format-3d-model-types/ The Main 3D Printing File Formats on all3dp]. &lt;br /&gt;
&lt;br /&gt;
STL is ideal for single-color models and maximum compatibility, while OBJ/MTL is recommended for multi-material workflows. 3MF files will be used in this tutorial to save the model and printing settings. &lt;br /&gt;
&lt;br /&gt;
Support in Proteopedia for these formats is based on the export capabilities of Jmol/JSmol; for details, see [http://wiki.jmol.org/index.php/File_formats/3D_Objects#STL STL] and [http://wiki.jmol.org/index.php/File_formats/3D_Objects#OBJ OBJ]&lt;br /&gt;
&lt;br /&gt;
== Overview of the 3D printing process ==&lt;br /&gt;
3D printing enables the transformation of atomic-level structural data into tangible macromolecular models that can be explored through both sight and touch.  &lt;br /&gt;
The process generally follows several main steps, each requiring specific types of software and hardware.&lt;br /&gt;
[[Image:3D_printing_workflow_v2.png|thumb|left|400px|Overview of the 3D printing workflow for generating physical molecular models.]]&lt;br /&gt;
	&lt;br /&gt;
=== Preparing the structure and generating a printable File ===&lt;br /&gt;
:The first stage involves creating a printable three-dimensional representation of the molecule. Some molecular-graphics programs such as [https://www.pymol.org/ PyMOL], [https://www.rbvi.ucsf.edu/chimerax/ UCSF ChimeraX], [https://molstar.org/Mol*], or [https://jmol.sourceforge.net/ Jmol] can be used not only to visualize a structure (from the Protein Data Bank or other sources), but also to export the resulting geometry in a .STL or .OBJ format. However, the default visualization styles of these programs are &#039;&#039;&#039;&#039;&#039;not directly suitable for 3D printing&#039;&#039;&#039;&#039;&#039;. Therefore, when preparing a model for fabrication, it is important to:&lt;br /&gt;
:* &#039;&#039;&#039;Select an appropriate molecular representation&#039;&#039;&#039; (e.g., surface, cartoon, sticks, spheres) depending on the pedagogical or structural feature you wish to highlight.  &lt;br /&gt;
:* &#039;&#039;&#039;Add struts or connectors&#039;&#039;&#039; to increase the mechanical stability of the model, especially for large complexes or long helices.  &lt;br /&gt;
:* &#039;&#039;&#039;Remove specific struts or pseudobonds&#039;&#039;&#039; when individual components — ligands, subunits, or cofactors — need to remain detachable.  &lt;br /&gt;
:* &#039;&#039;&#039;Adjust thickness&#039;&#039;&#039; of atoms, bonds, helices, and sheets to ensure adequate rigidity and printability (features thinner than the printer’s nozzle diameter or resin resolution may break).  &lt;br /&gt;
:* &#039;&#039;&#039;Apply meaningful coloring&#039;&#039;&#039; when preparing multi-material prints, for instance, to distinguish domains, chains, ligands or atoms.&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene that automates the process and enables users to effortlessly generate 3D-printable molecular models - more on that in the corresponding section [[#Generating printable files on Proteopedia|Generating printable files on Proteopedia]] within this page. For advanced users wanting to do this manually, we highly recommend two guides: &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_1&amp;quot; /&amp;gt; and &amp;lt;ref name=&amp;quot;3Dprinting_Proteins_Guide_2&amp;quot; /&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
=== Slicing the Model ===&lt;br /&gt;
Before printing, the STL file must be processed by a &#039;&#039;&#039;slicer&#039;&#039;&#039; — specialized software that converts 3D geometry into a series of horizontal layers. The slicer also generates &#039;&#039;&#039;G-code&#039;&#039;&#039;, the set of instructions that control the printer. These commands are printer-specific and include parameters such as extrusion speed, layer thickness, temperature, and movement. Together, they are usually stored as a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;.  &lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an FDM printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;number of perimeters&#039;&#039;&#039;, which affects mechanical strength and print time;&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines resolution and print duration;&lt;br /&gt;
:* &#039;&#039;&#039;infill density&#039;&#039;&#039;, which determines internal strength and affects print time;&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, temporary structures that hold overhanging regions;&lt;br /&gt;
:* &#039;&#039;&#039;print orientation&#039;&#039;&#039;, which influences surface quality, mechanical strength, and the amount of supports required.&lt;br /&gt;
:All these parameters make up a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. In this step, users must also select the material-specific parameters, or apply a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt;. More details on these profiles are provided later on this page.&lt;br /&gt;
&lt;br /&gt;
During the slicing of a molecular model for an &#039;&#039;&#039;SLA/DLP&#039;&#039;&#039; printer, users can adjust:&lt;br /&gt;
:* &#039;&#039;&#039;layer height&#039;&#039;&#039;, which determines vertical resolution and print time; thinner layers produce smoother surfaces but significantly increase printing duration.&lt;br /&gt;
:* &#039;&#039;&#039;exposure time&#039;&#039;&#039;, which controls how long each layer is cured by UV light; optimal exposure ensures proper adhesion between layers without over-curing fine details.&lt;br /&gt;
:* &#039;&#039;&#039;bottom-layer exposure and count&#039;&#039;&#039;, which influence model adhesion to the build platform — longer exposures and additional base layers improve stability during printing.&lt;br /&gt;
:* &#039;&#039;&#039;supports&#039;&#039;&#039;, which anchor the model to the build plate and prevent deformation during peeling; proper placement reduces surface marks and print failures.&lt;br /&gt;
:* &#039;&#039;&#039;model orientation&#039;&#039;&#039;, which affects surface quality, support contact area, and resin drainage; angling the model (typically 30–45°) minimizes suction forces and improves print reliability.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for FDM printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |An insulin model sliced for resin printing&lt;br /&gt;
|-&lt;br /&gt;
|[[Image:Insuline_sliced_prusa.gif|386px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|[[Image:Insuline_Sliced_SLA.gif|372px|center|thumb| Cartoon model of insulin, [[4ins]]]]&lt;br /&gt;
|-&lt;br /&gt;
|Cartoon model of insulin sliced in PrusaSlicer and ready to be printed on FDM printers. The arrow shows the trajectory of the print head on a single slice or layer. Orange is the model, green are the supports. &lt;br /&gt;
|Cartoon model of insulin sliced in Elegoo SatelLite and ready to be printed on FDM printer.On the left, with blue is the model, with gray are the supports. On the right is the image on the UV screen. &lt;br /&gt;
|} &lt;br /&gt;
&lt;br /&gt;
=== 3D Printing the Model ===&lt;br /&gt;
:The prepared G-code is then transferred to the 3D printer, either via an SD card, USB flash drive, or Wi-Fi connection. During printing, close observation of the first few layers is essential to ensure good adhesion to the build plate and a successful print. Total printing time depends on model size, selected layer height, and printer speed. &#039;&#039;Small peptide&#039;&#039; models may print in &#039;&#039;&#039;less than an hour&#039;&#039;&#039;, whereas l&#039;&#039;arge multimeric assemblies&#039;&#039; can require &#039;&#039;&#039;several hours or days&#039;&#039;&#039;. &#039;&#039;Multi-color&#039;&#039; or &#039;&#039;multi-material&#039;&#039; prints generally take &#039;&#039;&#039;longer&#039;&#039;&#039;, while &#039;&#039;SLA/DLP&#039;&#039; printers are generally &#039;&#039;&#039;faster&#039;&#039;&#039; due to their simultaneous layer exposure.&lt;br /&gt;
=== Post-Processing ===&lt;br /&gt;
:After printing, the model undergoes post-processing, which varies depending on the printing technology used:&lt;br /&gt;
:* For &#039;&#039;&#039;FDM prints&#039;&#039;&#039;, supports are removed mechanically, and surfaces can be smoothed by light sanding or polishing.&lt;br /&gt;
:* For &#039;&#039;&#039;resin prints&#039;&#039;&#039;, supports are removed mechanically, parts are washed in isopropanol to remove uncured resin and then exposed to UV light for final curing.&lt;br /&gt;
:Models printed in multiple parts can be assembled using cyanoacrylate or epoxy adhesive. Optional finishing steps (painting, labeling) can improve contrast between subunits or highlight functional regions.&lt;br /&gt;
&lt;br /&gt;
==Generating printable files on Proteopedia==&lt;br /&gt;
Proteopedia integrates a dedicated &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool within each molecular scene, enabling users to effortlessly generate 3D-printable molecular models directly from its pages. The tool is powered by [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;], a script that analyzes the structural data and automatically scales the model’s geometry to match the printable volume of a medium-size desktop 3D printer (e.g., Ender-3, 210×210×210 mm). During this process, the tool evaluates the molecular bounding box, atom radii, and bond lengths, then proportionally adjusts all dimensions to achieve a realistic and mechanically robust print scale — preserving scientific accuracy while ensuring manufacturability. For advanced users, [https://github.com/mariusmihasan/3DP-Jmol &#039;&#039;&#039;3DP-Jmol&#039;&#039;&#039;] may also be used in conjunction with the [https://jmol.sourceforge.net/ &#039;&#039;&#039;Jmol&#039;&#039;&#039;] program, providing full access to its scripting capabilities and advanced export features.&lt;br /&gt;
Step-by-step guide for automatic generation of printable files on Proteopedia&lt;br /&gt;
=== Open a molecular scene and access the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool ===&lt;br /&gt;
Navigate to any Proteopedia page (for example, [[Introduction_to_protein_structure]]). The corresponding 3D structure will load in the viewer on the right.  &lt;br /&gt;
Clicking any green link will activate a specific Proteopedia scene.&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_button_in_Proteopedia.png|thumb|left|400px|The &#039;&#039;&#039;Print3D&#039;&#039;&#039; button on a Proteopedia page]]&lt;br /&gt;
&lt;br /&gt;
At the bottom of the structure display window, locate and click the &#039;&#039;&#039;Print3D&#039;&#039;&#039; button. The tool will launch and begin analyzing the current molecular structure.  &lt;br /&gt;
This process may take some time to complete, depending on the size of the structure.  &lt;br /&gt;
Please wait until the message &#039;&#039;&#039;Analyzing structure...&#039;&#039;&#039; disappears and the next page is displayed — this marks the start of the two-step printing workflow.&lt;br /&gt;
=== Select a molecular representation and a printing scale ===&lt;br /&gt;
In this new page, some user input is required. Each option includes a short explanation; the key steps are outlined below, but feel free to explore and adopt the settings that best fit your use case.&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step1.png|thumb|left|400px|Selecting molecular representation and printing scale]]&lt;br /&gt;
&lt;br /&gt;
(1) &#039;&#039;&#039;Choose a molecular representation&#039;&#039;&#039; from the &#039;&#039;&#039;Scheme&#039;&#039;&#039; list, based on your goal:&lt;br /&gt;
* &#039;&#039;&#039;Backbone&#039;&#039;&#039;, &#039;&#039;&#039;Trace&#039;&#039;&#039;, or &#039;&#039;&#039;Ribbon&#039;&#039;&#039; — to emphasize secondary structure (effective for teaching protein folds).&lt;br /&gt;
* &#039;&#039;&#039;Surface&#039;&#039;&#039; — to highlight molecular topology and binding sites.&lt;br /&gt;
* &#039;&#039;&#039;Ball &amp;amp; Stick&#039;&#039;&#039; — atom-level detail for ligands or small molecules; usually impractical for large proteins or complexes.&lt;br /&gt;
* &#039;&#039;&#039;Proteopedia Scene&#039;&#039;&#039; — attempts to render the current page’s scene directly; may not work for all scenes.&lt;br /&gt;
&#039;&#039;Note:&#039;&#039; Some representations may be unavailable for a given structure because they are not printable in a reliable way.&lt;br /&gt;
&lt;br /&gt;
(2) In the &#039;&#039;&#039;Printer&#039;&#039;&#039; section, select whether you want a &#039;&#039;&#039;single-color&#039;&#039;&#039; or a &#039;&#039;&#039;multi-color&#039;&#039;&#039; print.&lt;br /&gt;
&lt;br /&gt;
(3) In the &#039;&#039;&#039;Printer scale&#039;&#039;&#039; section, set the desired size of the printed model. The tool constrains safe sizes based on the chosen representation and displays the physical dimensions (mm). &#039;&#039;&#039;Important! Please note the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;printer scale value in %&amp;lt;/span&amp;gt; as it is going to be required downstream in the next section of this workflow, [[#Printing files from Proteopedia|Printing files from Proteopedia]]&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
(4) When ready, click the green &#039;&#039;&#039;Make printer files&#039;&#039;&#039; button. Please wait patiently until the  &#039;&#039;Generating files for 3D printing of...&#039;&#039; message disappears and the final step is displayed.&lt;br /&gt;
&lt;br /&gt;
===Download the .STL or .OBJ files===&lt;br /&gt;
&lt;br /&gt;
[[Image:Print3D_step2.png|thumb|left|400px|Final step in generating printable files]]&lt;br /&gt;
&lt;br /&gt;
In this final page, a 3D preview of the generated model is displayed.&lt;br /&gt;
You can use the mouse to rotate, zoom, and inspect the model from different angles. If the result meets your needs, click the green (A) &#039;&#039;&#039;Download files&#039;&#039;&#039; button and save the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive containing the &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; files on your computer. If your model needs further improvements, hit the green (B) &#039;&#039;&#039;Same structure&#039;&#039;&#039; button to return to the previous screen and adjust your settings.&lt;br /&gt;
&lt;br /&gt;
 maybe a movie is better- need to decide ?&lt;br /&gt;
&lt;br /&gt;
{{clear}}&lt;br /&gt;
== Printing files from Proteopedia ==&lt;br /&gt;
Unzipping the compressed &#039;&#039;&#039;.zip&#039;&#039;&#039; archive will produce the exported &#039;&#039;&#039;.STL&#039;&#039;&#039; or &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file, along with an optional &#039;&#039;&#039;.MTL&#039;&#039;&#039; material file. &lt;br /&gt;
=== Using 3D printing services ===&lt;br /&gt;
If you do not have a 3D printer, you can still obtain physical models by using locally available 3D-printing services. Just search on [https://www.google.com/maps Google Maps] with the term  &#039;&#039;&#039;3D printing&#039;&#039;&#039; in your area. Here is short list of well-known 3D Printing service providers that may also ship worldwide: &lt;br /&gt;
&lt;br /&gt;
* [https://www.shapeways.com/ &#039;&#039;&#039;Shapeways&#039;&#039;&#039;] — global service offering a wide range of materials and colors. Educational discounts are available through their academic program.&lt;br /&gt;
* [https://www.sculpteo.com/en/ &#039;&#039;&#039;Sculpteo&#039;&#039;&#039;] — Europe-based provider offering fast turnaround and many printing technologies, including resin and polymer options.&lt;br /&gt;
* [https://www.xometry.com/capabilities/3d-printing-service &#039;&#039;&#039;Xometry&#039;&#039;&#039;] — large international network providing access to industrial-grade printing methods such as FDM, SLA, SLS, and DMLS.&lt;br /&gt;
* [https://craftcloud3d.com/ &#039;&#039;&#039;Craftcloud&#039;&#039;&#039;] — an aggregator that compares multiple providers and finds the best price and lead time for your uploaded model.&lt;br /&gt;
&lt;br /&gt;
When contacting a printing service, provide the exported files together with the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value in %&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ([[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). It is also advisable to share the link to this Proteopedia page so that the operator understands the peculiarities of printing molecular models. &lt;br /&gt;
&lt;br /&gt;
=== Using a desktop 3D printer ===&lt;br /&gt;
&lt;br /&gt;
Before importing the .STL or .OBJ file into your slicer software, it is recommended to inspect and, if necessary, repair the model to ensure printability. Common issues include non-manifold geometry, intersecting faces, and missing surfaces.  The example below demonstrates how to use [https://www.blender.org/ &#039;&#039;&#039;Blender&#039;&#039;&#039;] together with its [https://extensions.blender.org/add-ons/print3d-toolbox/ &#039;&#039;&#039;3D Print Toolbox extension&#039;&#039;&#039;] to improve the printability of the .STL and .OBJ files generated with the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool in [[Proteopedia]]. &#039;&#039;&#039;Important note&#039;&#039;&#039;: The repair process is largely automated but may introduce artifacts. Carefully inspect the corrected model for any missing or distorted sections, atoms, or bonds, and determine whether these omissions affect the intended purpose of the printed model.  &lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for single color or resin printing&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to fix the molecular models generated by Proteopedia for multi-color FDM printing&lt;br /&gt;
|-&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=k6u-5JnoP-c&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|&amp;lt;html5media height=&amp;quot;337&amp;quot; width=&amp;quot;600&amp;quot;&amp;gt;https://www.youtube.com/watch?v=OCisrIZMIDM&amp;lt;/html5media&amp;gt;&lt;br /&gt;
|}  &lt;br /&gt;
&lt;br /&gt;
Once the repaired &#039;&#039;&#039;.STL or .OBJ&#039;&#039;&#039; file is ready, it can be imported into your slicer software. In this step, you will prepare the file for printing by applying appropriate printer, filament, and print-settings profiles.&lt;br /&gt;
&lt;br /&gt;
*Apply the &amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;&#039;&#039;&#039;printer scale value (%)&#039;&#039;&#039;&amp;lt;/span&amp;gt; saved in the previous step ( [[#Select a molecular representation and a printing scale|Select a molecular representation and a printing scale]]). This step ensures that the model fits your print bed and maintains structural integrity during printing. The location of the scale (%) input field varies depending on the slicer software you are using.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Orient the model on the print bed&#039;&#039;&#039; so that its largest, flattest surface rests on the bed. This minimizes the need for supports and improves adhesion. If your slicer includes an Auto Orient or Auto Arrange function, use it to optimize placement. (&#039;&#039;Hint&#039;&#039;: Bambu Studio and Orca Slicer include this feature, Ultimaker Cura has a [https://marketplace.ultimaker.com/app/cura/plugins/nallath/OrientationPlugin Auto-Orientation plugin] available, while PrusaSlicer currently does not.)&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Select the printer&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that matches your device.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Choose the material&#039;&#039;&#039; by applying a &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; corresponding to the filament type (e.g., PLA, PETG, TPU) and manufacturer you intend to use.&lt;br /&gt;
&lt;br /&gt;
*&#039;&#039;&#039;Adjust the printing parameters&#039;&#039;&#039; by selecting a &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; that defines layer height, infill, speed, and support options.&lt;br /&gt;
&lt;br /&gt;
In most cases, the default &amp;lt;span style=&amp;quot;color:orange&amp;quot;&amp;gt;&#039;&#039;&#039;printer profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; and &amp;lt;span style=&amp;quot;color:purple&amp;quot;&amp;gt;&#039;&#039;&#039;filament profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; provided by the slicer are sufficient. However, molecular models often include overhangs, thin connections, and complex internal geometries, which require additional supports and reinforced perimeters to ensure structural stability. For this reason, the default &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;print settings profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; or &amp;lt;span style=&amp;quot;color:#008080&amp;quot;&amp;gt;&#039;&#039;&#039;process profile&#039;&#039;&#039;&amp;lt;/span&amp;gt; may not yield optimal results.&lt;br /&gt;
&lt;br /&gt;
Validated printing profiles for the &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool are available for several printer models. These profiles provide optimized settings that produce sturdy models, reduce material consumption, and shorten print time, ensuring consistent and reliable results. Three distinct profiles are supplied, corresponding to major molecular representations: &#039;&#039;&#039;balls and sticks&#039;&#039;&#039;, &#039;&#039;&#039;surface&#039;&#039;&#039;, and &#039;&#039;&#039;cartoon&#039;&#039;&#039;. The &#039;&#039;&#039;cartoon&#039;&#039;&#039; profile is also suitable for &#039;&#039;&#039;backbone&#039;&#039;&#039;, &#039;&#039;&#039;trace&#039;&#039;&#039;, and &#039;&#039;&#039;ribbon&#039;&#039;&#039; representations. For some printers, each profile is supplied in two variants, one using standard supports and one using tree or organic supports. In the case of multi-material printers, profiles for printing with soluble support and soluble interface are also provided.&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer brand and model&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Profiles provided as / Slicer&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |Printer Type, nozle size and multi-material support&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |GitHub with profiles&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; |How to import profiles into Slicer&lt;br /&gt;
|-&lt;br /&gt;
|Original Prusa Core One&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer ]&lt;br /&gt;
|FDM / 0.4 mm / yes, 5 colors, if MMU3 installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/Prusa%20CoreOne CoreOne]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab A1Mini&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, 4 colors if AMS Lite is installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/0c9c4fb7c2eee2f338dc4c94f0a5d01e00026587/BambuLab%20A1Mini AiMini]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|-&lt;br /&gt;
|BambuLab X1 Carbon&lt;br /&gt;
|a single Process preset .zip file with all presets / [https://bambulab.com/en-eu/download/studio Bambus Studio]&lt;br /&gt;
|FDM / 0.4 mm / yes, up to 16 colors if multiple AMS are installed&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ca92e7de9c72505c1b9b09e912ad177341cabc9a/BambuLab%20X1C X1Carbon]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in Bambus Studio]&lt;br /&gt;
|- &lt;br /&gt;
|Original Prusa MK3S+&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/7a7ee68d1e19f063600f53def49a99dfefbc595d/Prusa%20MK3S%2B MK3S+]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 5 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/a653c7cc6b3dec86b90117cc450d1883cc4a80bd/Ender-5-Pro Ender5Pro]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Creality Ender 3 v2 with a ENDERIDEX kit&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / yes, IDEX, two filaments&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/c2c74f1261a42c160e7e3898a407f21465de2ca7/Ender3-IDEX Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Kingroon KPS3 Pro&lt;br /&gt;
|a single profile per .INI file / [https://www.prusa3d.com/page/prusaslicer_424/ PrusaSlicer]&lt;br /&gt;
|FDM / 0.4 mm / no&lt;br /&gt;
|[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles/tree/ea733b2d05020b99f91c92f71a039c5ba8e54108/Kingroon-KPS3-Pro Ender3IDEX]&lt;br /&gt;
|[https://help.prusa3d.com/article/how-to-import-and-export-custom-profiles-in-prusaslicer_382766 Import and export custom profiles in PrusaSlicer]&lt;br /&gt;
|- &lt;br /&gt;
|Elegoo Mars 5 Ultra&lt;br /&gt;
|no profile needed, just be sure to add supports / [https://www.elegoo.com/pages/satellite-3d-slicer?srsltid=AfmBOopMQGHgHycHMFOZALzOIC8z7bVlSHjL_jj2ShYR4QkowYKmKzUx ELEGOO SatelLite]&lt;br /&gt;
|resin / - / no&lt;br /&gt;
|&lt;br /&gt;
|no profile needed, default settings worked, just be sure to add supports. EVO supports worked well enough.  Post processing steps: 1)washing: at least 10 min. 2) support removal 3)curring: at least 10 min on a Elegoo Mercury Plus V3.0&lt;br /&gt;
|- &lt;br /&gt;
|} &lt;br /&gt;
&#039;&#039;&#039;Notes&#039;&#039;&#039;: &lt;br /&gt;
* These profiles were developed and validated with the support of EDUMOL3D, Project [http://cercetare.bio.uaic.ro/grupuri/bioactive/content/grants/PED2024_mm.html PN-IV-P7-7.1-PED-2024-0343] financed by the Ministry of Research, Innovation and Digitization, [https://uefiscdi.gov.ro/ UEFISCDI], Romania.&lt;br /&gt;
* The profiles are a work in progress. Please check GitHub for updates. If you have suggestions for improvements, please drop a message at marius.mihasan(@)uaic.ro&lt;br /&gt;
&lt;br /&gt;
==== &#039;&#039;&#039;Note on multi-color printing &#039;&#039;&#039; ====&lt;br /&gt;
To our knowledge, only &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039; and &#039;&#039;&#039;Orca Slicer&#039;&#039;&#039; can automatically import color information from the &#039;&#039;&#039;.MTL&#039;&#039;&#039; file associated with the printable &#039;&#039;&#039;.OBJ&#039;&#039;&#039; generated by the Proteopedia &#039;&#039;&#039;Print3D&#039;&#039;&#039; tool.  &lt;br /&gt;
At present, &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; does not support importing &#039;&#039;&#039;.MTL&#039;&#039;&#039; files directly.&lt;br /&gt;
&lt;br /&gt;
A practical workaround for &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039; users is as follows:  &lt;br /&gt;
# Open the &#039;&#039;&#039;.OBJ&#039;&#039;&#039; file in &#039;&#039;&#039;Bambu Studio&#039;&#039;&#039;.  &lt;br /&gt;
#Verify or adjust the color mapping as needed.  &lt;br /&gt;
#Export the model as a generic &#039;&#039;&#039;.3MF&#039;&#039;&#039; file using the menu command:  &#039;&#039;File&#039;&#039; → &#039;&#039;Export&#039;&#039; → &#039;&#039;Export Generic 3MF...&#039;&#039;  &lt;br /&gt;
#Open the exported &#039;&#039;&#039;.3MF&#039;&#039;&#039; file in &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;. The color data will now be available under the &#039;&#039;&#039;Multimaterial Painting&#039;&#039;&#039; tool.&lt;br /&gt;
&lt;br /&gt;
This workflow preserves the original coloring assigned in Proteopedia and allows successful multi-color or multi-material printing on any capable 3D printer compatible with &#039;&#039;&#039;PrusaSlicer&#039;&#039;&#039;.&lt;br /&gt;
&lt;br /&gt;
== Other relevant resources ==&lt;br /&gt;
[Proteopedia gallery of 3D printed models] - examples of 3D printed molecular models from Proteopedia users.&lt;br /&gt;
&lt;br /&gt;
[https://3d.nih.gov/ NIH 3D Print Exchange] - an open, community-driven portal to download, share, and create bioscientific and medical 3D models, including for 3D printing.&lt;br /&gt;
  &lt;br /&gt;
[https://github.com/mariusmihasan/3DP-Jmol 3DP-Jmol] - the Jmol/JSmol behind the Print3D tool. Automatically generates 3D printable molecular models from structural data and can be easily integrated into web pages.&lt;br /&gt;
&lt;br /&gt;
[https://pdb101.rcsb.org/learn/3d-printing/pdb-structures-and-3d-printing 3D Printing on PDB101] - a quick guide on 3D printing molecular models and a small curated 3D models for education&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;If you print a model from Proteopedia, please share photos and feedback — let’s 3D print the whole Proteopedia!&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:3D printer files]]&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=User:Marius_Mihasan&amp;diff=4386095</id>
		<title>User:Marius Mihasan</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=User:Marius_Mihasan&amp;diff=4386095"/>
		<updated>2025-10-27T09:25:11Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;*[[User:Marius Mihasan/Print3D_help]]&lt;br /&gt;
*[[User:Marius Mihasan/Print3D_models_gallery]]&lt;br /&gt;
*[[User:Marius Mihasan/Workbench]]&lt;br /&gt;
*[[User:Marius Mihasan/Workbench/Print3Ddmodelsgallery]]&lt;br /&gt;
*[[User:Marius Mihasan/Sandbox 2]]&lt;br /&gt;
== &#039;&#039;&#039;Marius Mihasan&#039;&#039;&#039; ==&lt;br /&gt;
Professor, Lead, [http://cercetare.bio.uaic.ro/grupuri/bioactive/index.html BioActive Research Group]&lt;br /&gt;
&lt;br /&gt;
Biology Department, [https://www.uaic.ro/ Alexandru Ioan Cuza University of Iasi]&lt;br /&gt;
Carol I Bvd., N0.11, 700506, Iaşi, România&lt;br /&gt;
&#039;&#039;&#039;e-mail&#039;&#039;&#039;: &#039;&#039;marius(dot)mihasan(at)uaic(dot)ro&#039;&#039;&lt;br /&gt;
&#039;&#039;&#039;Tel:&#039;&#039;&#039; &#039;&#039;+40(0)232202434&#039;&#039;&lt;br /&gt;
&#039;&#039;&#039;Fax:&#039;&#039;&#039; &#039;&#039;+40(0)232201472&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Field of Expertise or Study: Biochemistry, 3D printing of macromolecular models.&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Resources for exploring the molecular universe with 3D printed models:&#039;&#039;&#039; &lt;br /&gt;
*[https://github.com/mariusmihasan/3DP-Jmol/tree/main 3DP-Jmol] - a script that automatically generates 3D printable molecular models from structural data.&lt;br /&gt;
*[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles molecularmodels-3d-printing-profiles] - A repository with validated 3D printing profiles for fabrication of molecular models generated with 3DP-Jmol or the Print3D tool in Proteopedia. Profiles available for Prusa Core One, Prusa MK3S+, Bambulab A1 Mini, Bambulab X1C, Creality Ender 5 Pro, Creality Ender 3 v2 with a ENDERIDEX kit, Kingroon KPS3 Pro&lt;br /&gt;
*[https://modelemoleculare.ro/ https://modelemoleculare.ro] -  a website with ready-to-print models and instruction. Romanian only, but it can be easily translated with Google.&lt;br /&gt;
* A collection of printed molecular models on [https://www.printables.com/@MariusMihasan_212025/models Printables]&lt;br /&gt;
--[[User:Marius Mihasan|Marius Mihasan]] 16:04, 25 April 2025 (UTC)&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=User:Marius_Mihasan&amp;diff=4382177</id>
		<title>User:Marius Mihasan</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=User:Marius_Mihasan&amp;diff=4382177"/>
		<updated>2025-10-11T05:49:51Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;*[[User:Marius Mihasan/Workbench]]&lt;br /&gt;
*[[User:Marius Mihasan/Workbench/Print3Ddmodelsgallery]]&lt;br /&gt;
*[[User:Marius Mihasan/Sandbox 2]]&lt;br /&gt;
== &#039;&#039;&#039;Marius Mihasan&#039;&#039;&#039; ==&lt;br /&gt;
Professor, Lead, [http://cercetare.bio.uaic.ro/grupuri/bioactive/index.html BioActive Research Group]&lt;br /&gt;
&lt;br /&gt;
Biology Department, [https://www.uaic.ro/ Alexandru Ioan Cuza University of Iasi]&lt;br /&gt;
Carol I Bvd., N0.11, 700506, Iaşi, România&lt;br /&gt;
&#039;&#039;&#039;e-mail&#039;&#039;&#039;: &#039;&#039;marius(dot)mihasan(at)uaic(dot)ro&#039;&#039;&lt;br /&gt;
&#039;&#039;&#039;Tel:&#039;&#039;&#039; &#039;&#039;+40(0)232202434&#039;&#039;&lt;br /&gt;
&#039;&#039;&#039;Fax:&#039;&#039;&#039; &#039;&#039;+40(0)232201472&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Field of Expertise or Study: Biochemistry, 3D printing of macromolecular models.&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Resources for exploring the molecular universe with 3D printed models:&#039;&#039;&#039; &lt;br /&gt;
*[https://github.com/mariusmihasan/3DP-Jmol/tree/main 3DP-Jmol] - a script that automatically generates 3D printable molecular models from structural data.&lt;br /&gt;
*[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles molecularmodels-3d-printing-profiles] - A repository with validated 3D printing profiles for fabrication of molecular models generated with 3DP-Jmol or the Print3D tool in Proteopedia. Profiles available for Prusa Core One, Prusa MK3S+, Bambulab A1 Mini, Bambulab X1C, Creality Ender 5 Pro, Creality Ender 3 v2 with a ENDERIDEX kit, Kingroon KPS3 Pro&lt;br /&gt;
*[https://modelemoleculare.ro/ https://modelemoleculare.ro] -  a website with ready-to-print models and instruction. Romanian only, but it can be easily translated with Google.&lt;br /&gt;
* A collection of printed molecular models on [https://www.printables.com/@MariusMihasan_212025/models Printables]&lt;br /&gt;
--[[User:Marius Mihasan|Marius Mihasan]] 16:04, 25 April 2025 (UTC)&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=User:Marius_Mihasan&amp;diff=4382176</id>
		<title>User:Marius Mihasan</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=User:Marius_Mihasan&amp;diff=4382176"/>
		<updated>2025-10-11T05:49:23Z</updated>

		<summary type="html">&lt;p&gt;Marius Mihasan: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;*[[User:Marius Mihasan/Workbench]]&lt;br /&gt;
*[[User:Marius Mihasan/Workbench/Print3Ddmodelsgallery]]&lt;br /&gt;
*[[User:Marius Mihasan/Sandbox 2]]&lt;br /&gt;
== &#039;&#039;&#039;Marius Mihasan&#039;&#039;&#039; ==&lt;br /&gt;
Professor, Lead, [http://cercetare.bio.uaic.ro/grupuri/bioactive/index.html BioActive Research Group]&lt;br /&gt;
&lt;br /&gt;
Biology Department, [https://www.uaic.ro/ Alexandru Ioan Cuza University of Iasi]&lt;br /&gt;
Carol I Bvd., N0.11, 700506, Iaşi, România&lt;br /&gt;
&#039;&#039;&#039;e-mail&#039;&#039;&#039;: &#039;&#039;marius(dot)mihasan(at)uaic(dot)ro&#039;&#039;&lt;br /&gt;
&#039;&#039;&#039;Tel:&#039;&#039;&#039; &#039;&#039;+40(0)232202434&#039;&#039;&lt;br /&gt;
&#039;&#039;&#039;Fax:&#039;&#039;&#039; &#039;&#039;+40(0)232201472&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Field of Expertise or Study: Biochemistry, 3D printing of macromolecular models.&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Resources for exploring the molecular universe with 3D printed models:&#039;&#039;&#039; &lt;br /&gt;
*[https://github.com/mariusmihasan/molecularmodels-3d-printing-profiles molecularmodels-3d-printing-profiles] - A repository with validated 3D printing profiles for fabrication of molecular models generated with 3DP-Jmol or the Print3D tool in Proteopedia. Profiles available for Prusa Core One, Prusa MK3S+, Bambulab A1 Mini, Bambulab X1C, Creality Ender 5 Pro, Creality Ender 3 v2 with a ENDERIDEX kit, Kingroon KPS3 Pro&lt;br /&gt;
*[https://github.com/mariusmihasan/3DP-Jmol/tree/main 3DP-Jmol] - a script that automatically generates 3D printable molecular models from structural data.&lt;br /&gt;
*[https://modelemoleculare.ro/ https://modelemoleculare.ro] -  a website with ready-to-print models and instruction. Romanian only, but it can be easily translated with Google.&lt;br /&gt;
* A collection of printed molecular models on [https://www.printables.com/@MariusMihasan_212025/models Printables]&lt;br /&gt;
--[[User:Marius Mihasan|Marius Mihasan]] 16:04, 25 April 2025 (UTC)&lt;/div&gt;</summary>
		<author><name>Marius Mihasan</name></author>
	</entry>
</feed>