Student Projects for UMass Chemistry 423 Spring 2012: Difference between revisions

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New page: ''' Spring 2012 Chem423 Team Projects: Protein-ligand Complexes for Understanding Drug and Disease Mechanisms''' == Project Instructions == '''1. Topics and 1 green scene: Sandbox pages...
 
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'''1. Topics and 1 green scene: Sandbox pages displaying initial structure and one green scene due at class workshop 2/27/12'''
'''1. Topics and 1 green scene: Sandbox pages displaying initial structure and one green scene due at class workshop 2/27/12'''
:'''Teams''' of 4 people will be assigned, to include both chemistry and chemical engineering majors on most teams. You may request one teammate by emailing the TA by Feb 17.  
:'''Teams''' of 4 people will be assigned, to include both chemistry and chemical engineering majors on most teams. You may request one teammate by emailing the TA by Feb 17.  
:Select an available '''topic''' (not already chosen by another team) from the list or find a simple protein-ligand complex (eg protein-drug, nucleic acid-drug, or protein-DNA) with a known structure in the pdb that interests your team.  For any topic not on the list, email Prof Thompson to get approval: send the pdb code for the complex and briefly explain the disease connection or why it is interesting.  
:Select an available '''topic''' (not already chosen by another team) from the list or find a simple protein-ligand complex (eg protein-drug, nucleic acid-drug, or protein-DNA) with a known structure in the pdb that interests your team.  For any topic not on the list, email Prof Thompson to get approval: send the pdb code for the complex and briefly explain the disease connection or why it is interesting. Add your topic to the team list at [[Sandbox 423]].


:'''Start your assigned sandbox page''': Find the pdb id for your protein-ligand complex in the Protein Data Bank. In your assigned sandbox page click"edit this page" (top) and follow the directions to insert your rotating structure on your page. Describe and illustrate with a green scene the secondary structure of your protein.
:'''Start your assigned sandbox page''': Find the pdb id for your protein-ligand complex in the Protein Data Bank. In your assigned sandbox page click"edit this page" (top) and follow the directions to insert your rotating structure on your page. Describe and illustrate with a green scene the secondary structure of your protein.


'''2. Project near-final draft, due 1 week before presentation.''' Prof Thompson will provide suggestions for improvements (you may also request feedback earlier, if you have all sections started and containing one green scene.
'''2. Project near-final draft, due 1 week before presentation. ''' Presentation dates will be assigned when topics are chosen. Prof Thompson will provide suggestions for improvements (you may also request feedback earlier, once you have at least one green scene with text describing it in all sections.
''Your proteopedia page should be organized into the following 4 required sections, with each team member responsible for one of these sections of the team project.''
''Your proteopedia page should be organized into the following 4 required sections, with each team member responsible for one of sections a-d of the team project.''
Each section should have its own jmol window. Provide an interesting and nontechnical description in words, and illustrate points about the complex with green scenes. Be concise: the written description should not extend beyond the jmol window.
Each section should have its own jmol window. Provide an interesting and nontechnical description in words, and illustrate points about the complex with green scenes. Be concise: the written description should not extend beyond the jmol window. Do not include any copyrighted figures. All sections must be written in your own words with citations to your sources, following the format in the example below. Make it interesting and accessible to a non-scientist!
a. Introduction
a. Introduction
:Introduce the protein function and the disease treated by the drug. This must be written in your own words with citations to your sources.You cannot include a copyrighted figure unless you request permission to use it.  
:Introduce the protein function, how it is related to a disease, and what is important about the ligand in the complex. Make a green scene suitable for the Molecular Playground: an attractive and informative illustration of the protein complex with an interesting short caption describing it.  
b. Overall structure
b. Overall structure
:Describe the overall structure of your protein in words and make "green scenes" to illustrate your points. What elements of secondary structure are present (ie 5 alpha helices and 2 beta strands) and how are they organized? Below I illustrate the start of an "overall structure" section on GFP. Additional description and green scenes could illustrate the polar/nonpolar distrubution of amino acids (is the inside of the barrel polar or nonpolar?), packing of amphipathic elements, etc.
:Describe the overall structure of your protein in words and make "green scenes" to illustrate your points. What elements of secondary structure are present (ie 5 alpha helices and 2 beta strands) and how are they organized? Additional description and green scenes could illustrate the polar/nonpolar distrubution of amino acids (is the inside of the barrel polar or nonpolar?), packing of amphipathic elements, etc.
c. Drug binding site
c. Drug binding site
:Describe features of the drug binding site in words and make "green scenes" to illustrate your points. Show the interactions that stabilize binding of this molecule to the protein (ie H bonds).
:Describe features of the drug or ligand binding site in words and make "green scenes" to illustrate your points. Show the interactions that stabilize binding of this molecule to the protein (ie H bonds).
d. Additional features
d. Additional features
:Describe and use green scenes to illustrate additional features of the protein. What you do here depends on what information is available. If a structure of the protein-substrate complex is available, you could compare protein interactions with the substrate vs. with the drug. If the drug is a transition state inhibitor, explain and illustrate that (eg include a reaction scheme with structures of the substrate, transition state and product).
:Describe and use green scenes to illustrate additional features of the protein. What you do here depends on what information is available. If a structure of the protein-substrate complex is available, you could compare protein interactions with the substrate vs. with the drug. If the drug is a transition state inhibitor, explain and illustrate that (eg include a reaction scheme with structures of the substrate, transition state and product -- but don't borrow a published scheme).


e. Credits -- at the end list who did which portion of the project:
e. Credits -- at the end list who did which portion of the project:
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This will include the published paper that describes your structure (the reference associated with your pdb code). You will get much of your information about specific interactions to look for and highlight in the structure from this reference (which is much easier than trying to find these on your own with no guidance!).
This will include the published paper that describes your structure (the reference associated with your pdb code). You will get much of your information about specific interactions to look for and highlight in the structure from this reference (which is much easier than trying to find these on your own with no guidance!).


'''3. In-class presentations, to be announced'''
'''3. In-class presentations on assigned dates."''


== Example ==
== Example ==
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<references/>
<references/>


== Project Teams, Topics, Links, and Presentation Dates ==
'''C''' See comment on your page.
Example (but not a drug complex): Lynmarie Thompson, ..., ..., ... - Asp receptor in complex with Asp (above)
Monday 4/25/11
Nick DeGraan-Weber, Jackie Dorhout, Rachael Jayne, Mike Reardon - [[#Flu Neuraminidase|flu neuraminidase in complex with tamiflu]]
John Hickey, Josh Drolet, Josephine Harrington, Andrea Simoni - [[#Influenza M2 Proton Channel|influenza M2 proton channel]]
[[UMass Chem 423 Student Projects 2011-1]]:
Wednesday 4/27/11
Brittany Forkus, Katie Geldart, Elizabeth Schutsky, Breanna Zerfas - Beta Adrenergic GPCR
Lucia Tringali, Shaina Boyle, Jaclyn Somadelis , Dany Mbakop -- HIV Protease
Andy Kim, Zach Brentzel, Tyler Vlass, Zach Hitzig -- Acetylcholinesterase
Friday 4/29/11
Varun Chalupadi, Anthony Laviola, Tiffany Brucker, Alan Stebbins - Cyclooxygenase
[[UMass Chem 423 Student Projects 2011-2]]:
Inna Brockman, Robert Nathan, Sarena Horava, Nick Cadirov - p38 kinase
David Peltier, Donald Einck, Ethan Leighton, Chris Coakley - Rituximab Fab
Monday 5/2/11
Max Moulton, Sally Stras, Jordan Schleeweis, Anh Huynh  -- HIV reverse transcription
Chris Brueckner, Daniel Roy, John Clarkson, Justin Srodulski -- Ketamine in binding complex with NMDA receptor
Lyes Khendek, Paul Breslin, William Rowley, Joe Perito, Ashley Rivera - G-Quadruplex
==Students looking for group members==
Each group should contain at least one person from a different primary major (typically Chemistry or Chemical Engineering) than the rest.
List yourself + your major, list partial groups looking for members, list your complex if you have chosen one. Contact others to form a group.
4/1/11 update by Prof Thompson: The remaining students can go ahead and form teams regardless of major.
Luis Cristian, Chem major, lcristia@student.umass.edu - looking to be in a group with chem eng


==Help Editing==
==Help Editing==
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Some of the above are for help editing Wikipedia pages, but the syntax is mostly the same. Proteopedia ADDS protein stuff to the WikiMedia markup language, which powers both WEB sites.
Some of the above are for help editing Wikipedia pages, but the syntax is mostly the same. Proteopedia ADDS protein stuff to the WikiMedia markup language, which powers both WEB sites.
==Questions & Answers==
Here is a place to post questions and answers for each other about how to do things in Proteopedia:
A very useful color scheme is "chain" which colors separate proteins or DNA strands in different colors (first select all protein or DNA).
Anyone know what format we should be putting our references in?
For references, follow the format used in the example on the Asp receptor and they will be put in automatically.
You just find out the PMID code (listed in pubmed for example) and insert it into the following, at the place where you want the reference cited (click edit to see what is actually inserted here).
<ref>PMID: 8486661</ref>
You also need to add the section:
'''References'''
<references/>
Hey guys this is just a useful tip:
If you get an xml error after you try to save your changes it is due to the green scene coding. Our group experienced this issue and it would not let us access our sandbox. In order to fix this go back (or find the page to edit in your history) and delete the green scene code that was just entered. Then save the page and you should be back to your sandbox. This may be trivial to many, but just throwing it out there.
To highlight some interesting portion of your protein:
Under the selections tab, you can "limit to residue numbers." So for example enter in 60-65, then click "replace selection" below. Then if you go to the colors tab you can pick a color for just the residues you have selected. If it is a loop or if they are hard to see you can go to the representation tab and set selection to ball and stick or spacefill.
It is also useful to click the "selection halos:" box under the picture. That shows you what you have in your selection.