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	<id>https://proteopedia.org/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Lauren+Jansen</id>
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	<updated>2026-10-04T11:58:01Z</updated>
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		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2356378</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2356378"/>
		<updated>2015-01-19T22:55:27Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: /* Integrins and cancer */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Studying integrin-mediated metastasis &#039;&#039;in vitro&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Glycosylated integrin Beta 1 (green and yellow), Alpha 5 (grey and pink), Fab light chain (aqua and magenta), Fab heavy chain (red and cyan) complex with RGD peptide (gold and wheat), Ca+2 and Mg+2 ions (PDB code [[3vi4]]).&#039; scene=&#039;&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
&#039;&#039;&#039;Integrins&#039;&#039;&#039; are surface proteins that are comprised of an alpha subunit and a beta subunit to form a functional transmembrane structure. The subunits of the heterodimer each have small cytoplasmic domains for signal transduction within the cell. There are 18 alpha and eight beta subunits in mammals. Different pairs of these alpha and beta subunits uniquely bind to extracellular proteins. Integrins connect the extracellular environment to the inside of a cell by inducing signals that affect cell functions. &lt;br /&gt;
&lt;br /&gt;
The protein structure on the right has the following color coding: Blue-Alpha 5 chain, Red-Beta 1 chain, Grey-SG/19 Fab fragment light chain, Green-SG/19 Fab fragment heavy chain.&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extracellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including &amp;lt;scene name=&#039;60/609772/Integrinbeta1_binding_collagen/1&#039;&amp;gt;collagen&amp;lt;/scene&amp;gt;, laminin and fibronectin.  Integrin adhesion to the extra cellular matrix is key for cell ability to adhere, migrate and proliferate in both 2D and 3D systems. These will eventually form adhesion complexes, which regulate actomyocin polymerization. During migration, cells continually form new focal adhesions at the leading edge of the cell and release adhesion complexes at the back of the cell, enabling forward movement.&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt; N-acetyl-D-glucosamine may regulate integrin signaling during cancer cell migration&amp;lt;ref&amp;gt;PMID:19755493&amp;lt;/ref&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
[[Image:Integrin.png|200 px|thumb|Fig. 1: Schematic of integrin heterodimers binding to ECM proteins]]&lt;br /&gt;
&lt;br /&gt;
==Integrins and cancer==&lt;br /&gt;
&lt;br /&gt;
Integrins binding to the extracellular matrix provide cells the ability to migrate and remodel the surrounding microenvironment. Integrins are extremely important in cancer metastasis and the progression of solid tumors. Cells bind to extracellular matrix proteins, like&amp;lt;scene name=&#039;60/609772/Rgd_bound/2&#039;&amp;gt; peptide RGD (black) on fibronectin&amp;lt;/scene&amp;gt;, with integrins to stimulate survival, migration/invasion, and proliferation  &amp;lt;ref&amp;gt;PMID:20029421&amp;lt;/ref&amp;gt;. Though high expression of integrin beta 1 has been shown to drive primary tumor progression and metastasis, targeting integrins for cancer treatment has seen limited clinical efficacy &amp;lt;ref&amp;gt;PMID:22894137&amp;lt;/ref&amp;gt;. These failures stem from differential integrin expression between cancer cells, but new technologies to screen cancer cell populations are being developed to affective therapies on a patient-specific level &amp;lt;ref&amp;gt; PMID: 25537447&amp;lt;/ref&amp;gt;. These technologies will likely allow for more selective treatment and better clinical efficacy for integrin inhibitors. &lt;br /&gt;
[[Image:B1_tissue.png|200 px|thumb|Fig. 2: Beta1 integrin expression in a human breast tumor stained in the Peyton Lab. Beta1 integrin (red) is expressed in the tumor cells. DAPI stains the nuclei in blue.]]&lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
Due to their roles in both disease and cell-matrix interactions, there is a growing interest in studying integrin function &#039;&#039;in vitro&#039;&#039;. Common approaches use simple end point gene or protein expression analysis, however, &#039;&#039;in vitro&#039;&#039; studies allow for functional analysis to observe intern binding interactions in single living cells. Tools include siRNA to prevent integrin gene expression, integrin binding peptides (i.e., the RGD peptide) which bind to integrins competitively with ECM proteins)&amp;lt;ref&amp;gt;PMID:7955174&amp;lt;/ref&amp;gt;, and function-affecting antibodies which can bind to integrin heterodimers and prevent binding to the ECM&amp;lt;ref&amp;gt;PMID:9105051 &amp;lt;/ref&amp;gt;. When beta1 dimerizes with alpha1, it can bind to both collagens I and IV as well as laminins &amp;lt;ref&amp;gt;PMID: 12662928&amp;lt;/ref&amp;gt;, which are both large components of the ECM of many tissues. Integrin alpha1 beta1 binding to a function affecting integrin antibody is shown &amp;lt;scene name=&#039;60/609777/With_antibody/4&#039;&amp;gt;here. Chains A and B of the I domain are blue, and the heavy and light chains of the Fab fragment are red. &amp;lt;/scene&amp;gt; These tools are especially useful when microenvironment stiffness&amp;lt;ref&amp;gt;PMID:20939067&amp;lt;/ref&amp;gt; or composition&amp;lt;ref&amp;gt;PMID:15183609&amp;lt;/ref&amp;gt; are controlled, allowing for examination of the effect of each of these cues on cell phenotype&amp;lt;ref&amp;gt;PMID:8074327&amp;lt;/ref&amp;gt; or downstream signaling. &lt;br /&gt;
&lt;br /&gt;
[[Image:231_beta1.png|315 px|thumb|Fig. 3: Beta1 integrin expression in the human breast cancer cell line MDA-MB-231 stained in the Peyton Lab. Beta1 integrin (green) is expressed mainly around the periphery. DAPI stains the nuclei in blue. Scale bar is 50 microns.]]&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. We are further interested in how integrins can be biomarkers in disease, because they transduce signals from the diseased microenvironment to cells, likely facilitating disease progression in some cases.&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065899</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065899"/>
		<updated>2014-11-21T14:34:04Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Studying integrin-mediated metastasis &#039;&#039;in vitro&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Integrin Beta 1 Alpha 5&#039; scene=&#039;60/609772/Integrinb1alpha5/1&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
Integrins are surface proteins that are comprised of an alpha subunit and a beta subunit to form a functional transmembrane structure. The subunits of the heterodimer each have small cytoplasmic domains for signal transduction within the cell.  &lt;br /&gt;
&lt;br /&gt;
The picture to the side has the following color coding: Blue-Alpha 5 chain, Red-Beta 1 chain, Grey-SG/19 Fab fragment light chain, Green-SG/19 Fab fragment heavy chain&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extracellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including &amp;lt;scene name=&#039;60/609772/Integrinbeta1_binding_collagen/1&#039;&amp;gt;collagen&amp;lt;/scene&amp;gt;, laminin and fibronectin.  Integrin adhesion to the extra cellular matrix is key for cell ability to adhere, migrate and proliferate in both 2D and 3D systems. These will eventually form adhesion complexes, which regulate actomyocin polymerization. During migration, cells continually form new focal adhesions at the leading edge of the cell and release adhesion complexes at the back of the cell, enabling forward movement.&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt; N-acetyl-D-glucosamine may regulate integrin signaling during cancer cell migration&amp;lt;ref&amp;gt;PMID:19755493&amp;lt;/ref&amp;gt;.&lt;br /&gt;
&lt;br /&gt;
==Integrins and cancer==&lt;br /&gt;
&lt;br /&gt;
Integrins binding to the extracellular matrix provide cells the ability to migrate and remodel the surrounding microenvironment. Integrins are extremely important in cancer metastasis and the progression of solid tumors. Cells bind to extracellular matrix proteins, like&amp;lt;scene name=&#039;60/609772/Rgd_bound/2&#039;&amp;gt; peptide RGD (black) on fibronectin&amp;lt;/scene&amp;gt;, with integrins to stimulate survival, migration/invasion, and proliferation  &amp;lt;ref&amp;gt;PMID:20029421&amp;lt;/ref&amp;gt;. Though high expression of integrin beta 1 has been shown to drive primary tumor progression and metastasis, targeting integrins for cancer treatment has seen limited clinical efficacy &amp;lt;ref&amp;gt;PMID:22894137&amp;lt;/ref&amp;gt;. These failures stem from differential integrin expression between cancer cells, but new technologies to screen cancer cell populations are being developed to affective therapies on a patient-specific level &amp;lt;ref&amp;gt; Barney LE, Dandley EC, Jansen LE, Reich NG, Mercurio AM, Peyton SR. “A Cell-ECM Screening Method to Predict Breast Cancer Metastasis”. (2014) In Review.&amp;lt;/ref&amp;gt;. These technologies will likely allow for more selective treatment and better clinical efficacy for integrin inhibitors. &lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
Due to their roles in both disease and cell-matrix interactions, there is a growing interest in studying integrin function &#039;&#039;in vitro&#039;&#039;. Common approaches use simple end point gene or protein expression analysis, however, &#039;&#039;in vitro&#039;&#039; studies allow for functional analysis to observe intern binding interactions in single living cells. Tools include siRNA to prevent integrin gene expression, integrin binding peptides (i.e., the RGD peptide) which bind to integrins competitively with ECM proteins)&amp;lt;ref&amp;gt;PMID:7955174&amp;lt;/ref&amp;gt;, and function-affecting antibodies which can bind to integrin heterodimers and prevent binding to the ECM&amp;lt;ref&amp;gt;PMID:9105051 &amp;lt;/ref&amp;gt;. When beta1 dimerizes with alpha1, it can bind to both collagens I and IV as well as laminins &amp;lt;ref&amp;gt;PMID: 12662928&amp;lt;/ref&amp;gt;, which are both large components of the ECM of many tissues. Integrin alpha1 beta1 binding to a function affecting integrin antibody is shown &amp;lt;scene name=&#039;60/609777/With_antibody/4&#039;&amp;gt;here. Chains A and B of the I domain are blue, and the heavy and light chains of the Fab fragment are red. &amp;lt;/scene&amp;gt; These tools are especially useful when microenvironment stiffness&amp;lt;ref&amp;gt;PMID:20939067&amp;lt;/ref&amp;gt; or composition&amp;lt;ref&amp;gt;PMID:15183609&amp;lt;/ref&amp;gt; are controlled, allowing for examination of the effect of each of these cues on cell phenotype&amp;lt;ref&amp;gt;PMID:8074327&amp;lt;/ref&amp;gt; or downstream signaling. &lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. We are further interested in how integrins can be biomarkers in disease, because they transduce signals from the diseased microenvironment to cells, likely facilitating disease progression in some cases.&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065665</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065665"/>
		<updated>2014-11-19T20:37:18Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Studying integrin-mediated metastasis &#039;&#039;in vitro&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Integrin Beta 1 Alpha 5&#039; scene=&#039;60/609772/Integrinb1alpha5/1&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
Blue-Alpha 5 chain&lt;br /&gt;
Red-Beta 1 chain&lt;br /&gt;
Grey-SG/19 Fab fragment light chain&lt;br /&gt;
Green-SG/19 Fab fragment heavy chain&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extracellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including collagen, laminin and fibronectin.  Integrin adhesion to the extra cellular matrix is key for cell ability to adhere, migrate and proliferate in both 2D and 3D systems. These will eventually form adhesion complexes, which regulate actomyocin polymerization. During migration, cells continually form new focal adhesions at the leading edge of the cell and release adhesion complexes at the back of the cell, enabling forward movement.&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt; N-acetyl-D-glucosamine may regulate integrin signaling during cancer cell migration.[1]&lt;br /&gt;
&lt;br /&gt;
==Integrins and cancer==&lt;br /&gt;
&lt;br /&gt;
Integrins binding to the extracellular matrix provide cells the ability to migrate and remodel the surrounding microenvironment. Integrins are extremely important in cancer metastasis and the progression of solid tumors. Cells bind to extracellular matrix proteins, like&amp;lt;scene name=&#039;60/609772/Rgd_bound/2&#039;&amp;gt; peptide RGD (black) on fibronectin&amp;lt;/scene&amp;gt;, with integrins to stimulate survival, migration/invasion, and proliferation  [2]. Though high expression of integrin beta 1 has been shown to drive primary tumor progression and metastasis, targeting integrins for cancer treatment has seen limited clinical efficacy [3]. These failures stem from differential integrin expression between cancer cells, but new technologies to screen cancer cell populations are being developed to affective therapies on a patient-specific level [4]. These technologies will likely allow for more selective treatment and better clinical efficacy for integrin inhibitors. &lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. &lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
==References==&lt;br /&gt;
[1] C. Saravanan, F. Liu, I.K. Gipson and N. Panjwani1. Galectin-3 promotes lamellipodia formation in epithelial cells by interacting with complex N-glycans on 31 integrin. Journal of Cell Science 122, 3684-3693 Published by The Company of Biologists (2009). doi:10.1242/jcs.045674.&lt;br /&gt;
&lt;br /&gt;
[2] Desgrossellier JS,  and Cheresh DA. Integrins in cancer: biological implications and therapeutic opportunities. Nature Reviews Cancer 10, 9-22 (January 2010) | doi:10.1038/nrc2748&lt;br /&gt;
&lt;br /&gt;
[3]Dos Santos PB, Zanetti JS, Ribeiro-Silva A, Beltrão EIC. Beta 1 integrin predicts survival in breast cancer: a clinicopathological and immunohistochemical study. Diagn Pathol 7:104.(2012)&lt;br /&gt;
&lt;br /&gt;
[4] Barney LE, Dandley EC, Jansen LE, Reich NG, Mercurio AM, Peyton SR. “A Cell-ECM Screening Method to Predict Breast Cancer Metastasis”. (2014) In Review.&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065664</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065664"/>
		<updated>2014-11-19T20:34:02Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Studying integrin-mediated metastasis &#039;&#039;in vitro&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Integrin Beta 1 Alpha 5&#039; scene=&#039;60/609772/Integrinb1alpha5/1&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
Blue-Alpha 5 chain&lt;br /&gt;
Red-Beta 1 chain&lt;br /&gt;
Grey-SG/19 Fab fragment light chain&lt;br /&gt;
Green-SG/19 Fab fragment heavy chain&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extracellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including collagen, laminin and fibronectin.  Integrin adhesion to the extra cellular matrix is key for cell ability to adhere, migrate and proliferate in both 2D and 3D systems. These will eventually form adhesion complexes, which regulate actomyocin polymerization. During migration, cells continually form new focal adhesions at the leading edge of the cell and release adhesion complexes at the back of the cell, enabling forward movement.&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt; N-acetyl-D-glucosamine may regulate integrin signaling during cancer cell migration.[1]&lt;br /&gt;
&lt;br /&gt;
==Integrins and cancer==&lt;br /&gt;
&lt;br /&gt;
Integrins binding to the extracellular matrix provide cells the ability to migrate and remodel the surrounding microenvironment. For these reasons, integrins are extremely important in cancer metastasis, and the progression of solid tumors. Cells bind to extracellular matrix proteins, like&amp;lt;scene name=&#039;60/609772/Rgd_bound/2&#039;&amp;gt; peptide RGD (black) on fibronectin&amp;lt;/scene&amp;gt;, with integrins to stimulate survival, migration/invasion, and proliferation  [2]. High expression of integrin beta 1 has been shown to drive primary tumor progression and metastasis, but targeting integrins for cancer treatment has seen limited success [3]. Likely, these failures stem from differential integrin expression between cancer cells, and new technologies to screen cancer cell populations are being developed to screen for affective therapies [4]. These technologies will likely allow for more selective treatment and better clinical efficacy for integrin inhibitors. &lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. &lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
==References==&lt;br /&gt;
[1] C. Saravanan, F. Liu, I.K. Gipson and N. Panjwani1. Galectin-3 promotes lamellipodia formation in epithelial cells by interacting with complex N-glycans on 31 integrin. Journal of Cell Science 122, 3684-3693 Published by The Company of Biologists (2009). doi:10.1242/jcs.045674.&lt;br /&gt;
&lt;br /&gt;
[2] Desgrossellier JS,  and Cheresh DA. Integrins in cancer: biological implications and therapeutic opportunities. Nature Reviews Cancer 10, 9-22 (January 2010) | doi:10.1038/nrc2748&lt;br /&gt;
&lt;br /&gt;
[3]Dos Santos PB, Zanetti JS, Ribeiro-Silva A, Beltrão EIC. Beta 1 integrin predicts survival in breast cancer: a clinicopathological and immunohistochemical study. Diagn Pathol 7:104.(2012)&lt;br /&gt;
&lt;br /&gt;
[4] Barney LE, Dandley EC, Jansen LE, Reich NG, Mercurio AM, Peyton SR. “A Cell-ECM Screening Method to Predict Breast Cancer Metastasis”. (2014) In Review.&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065663</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065663"/>
		<updated>2014-11-19T20:33:10Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
==Studying integrin-mediated metastasis &#039;&#039;in vitro&#039;&#039;==&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Integrin Beta 1 Alpha 5&#039; scene=&#039;60/609772/Integrinb1alpha5/1&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
Blue-Alpha 5 chain&lt;br /&gt;
Red-Beta 1 chain&lt;br /&gt;
Grey-SG/19 Fab fragment light chain&lt;br /&gt;
Green-SG/19 Fab fragment heavy chain&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extracellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including collagen, laminin and fibronectin.  Integrin adhesion to the extra cellular matrix is key for cell ability to adhere, migrate and proliferate in both 2D and 3D systems. These will eventually form adhesion complexes, which regulate actomyocin polymerization. During migration, cells continually form new focal adhesions at the leading edge of the cell and release adhesion complexes at the back of the cell, enabling forward movement.&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt; N-acetyl-D-glucosamine may regulate integrin signaling during cancer cell migration.[1]&lt;br /&gt;
&lt;br /&gt;
==Integrins and cancer==&lt;br /&gt;
&lt;br /&gt;
Integrins binding to the extracellular matrix provide cells the ability to migrate and remodel the surrounding microenvironment. For these reasons, integrins are extremely important in cancer metastasis, and the progression of solid tumors. Cells bind to extracellular matrix proteins, like&amp;lt;scene name=&#039;60/609772/Rgd_bound/2&#039;&amp;gt; peptide RGD (black) on fibronectin&amp;lt;/scene&amp;gt;, with integrins to stimulate survival, migration/invasion, and proliferation  [2]. High expression of integrin beta 1 has been shown to drive primary tumor progression and metastasis, but targeting integrins for cancer treatment has seen limited success [3]. Likely, these failures stem from differential integrin expression between cancer cells, and new technologies to screen cancer cell populations are being developed to screen for affective therapies [4]. These technologies will likely allow for more selective treatment and better clinical efficacy for integrin inhibitors. &lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. &lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
==References==&lt;br /&gt;
[1] C. Saravanan, F. Liu, I.K. Gipson and N. Panjwani1. Galectin-3 promotes lamellipodia formation in epithelial cells by interacting with complex N-glycans on 31 integrin. Journal of Cell Science 122, 3684-3693 Published by The Company of Biologists (2009). doi:10.1242/jcs.045674.&lt;br /&gt;
&lt;br /&gt;
[2] Desgrossellier JS,  and Cheresh DA. Integrins in cancer: biological implications and therapeutic opportunities. Nature Reviews Cancer 10, 9-22 (January 2010) | doi:10.1038/nrc2748&lt;br /&gt;
&lt;br /&gt;
[3]Dos Santos PB, Zanetti JS, Ribeiro-Silva A, Beltrão EIC. Beta 1 integrin predicts survival in breast cancer: a clinicopathological and immunohistochemical study. Diagn Pathol 7:104.(2012)&lt;br /&gt;
&lt;br /&gt;
[4] Barney LE, Dandley EC, Jansen LE, Reich NG, Mercurio AM, Peyton SR. “A Cell-ECM Screening Method to Predict Breast Cancer Metastasis”. (2014) In Review.&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065662</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065662"/>
		<updated>2014-11-19T20:30:37Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Cancer cell migration, Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Integrin Beta 1 Alpha 5&#039; scene=&#039;60/609772/Integrinb1alpha5/1&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
Blue-Alpha 5 chain&lt;br /&gt;
Red-Beta 1 chain&lt;br /&gt;
Grey-SG/19 Fab fragment light chain&lt;br /&gt;
Green-SG/19 Fab fragment heavy chain&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extracellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including collagen, laminin and fibronectin.  Integrin adhesion to the extra cellular matrix is key for cell ability to adhere, migrate and proliferate in both 2D and 3D systems. These will eventually form adhesion complexes, which regulate actomyocin polymerization. During migration, cells continually form new focal adhesions at the leading edge of the cell and release adhesion complexes at the back of the cell, enabling forward movement.&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt; N-acetyl-D-glucosamine may regulate integrin signaling during cancer cell migration.[1]&lt;br /&gt;
&lt;br /&gt;
==Integrins and cancer==&lt;br /&gt;
&lt;br /&gt;
Integrins binding to the extracellular matrix provide cells the ability to migrate and remodel the surrounding microenvironment. For these reasons, integrins are extremely important in cancer metastasis, and the progression of solid tumors. Cells bind to extracellular matrix proteins, like&amp;lt;scene name=&#039;60/609772/Rgd_bound/2&#039;&amp;gt; peptide RGD (black) on fibronectin&amp;lt;/scene&amp;gt;, with integrins to stimulate survival, migration/invasion, and proliferation  [2]. High expression of integrin beta 1 has been shown to drive primary tumor progression and metastasis, but targeting integrins for cancer treatment has seen limited success [3]. Likely, these failures stem from differential integrin expression between cancer cells, and new technologies to screen cancer cell populations are being developed to screen for affective therapies [4]. These technologies will likely allow for more selective treatment and better clinical efficacy for integrin inhibitors. &lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. &lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
[1] C. Saravanan, F. Liu, I.K. Gipson and N. Panjwani1. Galectin-3 promotes lamellipodia formation in epithelial cells by interacting with complex N-glycans on 31 integrin. Journal of Cell Science 122, 3684-3693 Published by The Company of Biologists (2009). doi:10.1242/jcs.045674.&lt;br /&gt;
&lt;br /&gt;
[2] Desgrossellier JS,  and Cheresh DA. Integrins in cancer: biological implications and therapeutic opportunities. Nature Reviews Cancer 10, 9-22 (January 2010) | doi:10.1038/nrc2748&lt;br /&gt;
&lt;br /&gt;
[3]Dos Santos PB, Zanetti JS, Ribeiro-Silva A, Beltrão EIC. Beta 1 integrin predicts survival in breast cancer: a clinicopathological and immunohistochemical study. Diagn Pathol 7:104.(2012)&lt;br /&gt;
&lt;br /&gt;
[4] Barney LE, Dandley EC, Jansen LE, Reich NG, Mercurio AM, Peyton SR. “A Cell-ECM Screening Method to Predict Breast Cancer Metastasis”. (2014) In Review.&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065661</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065661"/>
		<updated>2014-11-19T20:28:58Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Cancer cell migration, Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Integrin Beta 1 and Alpha 5&#039; scene=&#039;60/609772/Integrinb1alpha5/1&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
Blue-Alpha 5 chain&lt;br /&gt;
Red-Beta 1 chain&lt;br /&gt;
Grey-SG/19 Fab fragment light chain&lt;br /&gt;
Green-SG/19 Fab fragment heavy chain&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extracellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including collagen, laminin and fibronectin.  Integrin adhesion to the extra cellular matrix is key for cell ability to adhere, migrate and proliferate in both 2D and 3D systems. These will eventually form adhesion complexes, which regulate actomyocin polymerization. During migration, cells continually form new focal adhesions at the leading edge of the cell and release adhesion complexes at the back of the cell, enabling forward movement.&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt; N-acetyl-D-glucosamine may regulate integrin signaling during cancer cell migration.[1]&lt;br /&gt;
&lt;br /&gt;
==Integrins and cancer==&lt;br /&gt;
&lt;br /&gt;
Integrins binding to the extracellular matrix provide cells the ability to migrate and remodel the surrounding microenvironment. For these reasons, integrins are extremely important in cancer metastasis, and the progression of solid tumors. Cells bind to extracellular matrix proteins, like&amp;lt;scene name=&#039;60/609772/Rgd_bound/2&#039;&amp;gt;RGD (black) on fibronectin&amp;lt;/scene&amp;gt;, with integrins to stimulate survival, migration/invasion, and proliferation  [2]. High expression of integrin beta 1 has been shown to drive primary tumor progression and metastasis, but targeting integrins for cancer treatment has seen limited success [3]. Likely, these failures stem from differential integrin expression between cancer cells, and new technologies to screen cancer cell populations are being developed to screen for affective therapies [4]. These technologies will likely allow for more selective treatment and better clinical efficacy for integrin inhibitors. &lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. &lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
[1] C. Saravanan, F. Liu, I.K. Gipson and N. Panjwani1. Galectin-3 promotes lamellipodia formation in epithelial cells by interacting with complex N-glycans on 31 integrin. Journal of Cell Science 122, 3684-3693 Published by The Company of Biologists (2009). doi:10.1242/jcs.045674.&lt;br /&gt;
&lt;br /&gt;
[2] Desgrossellier JS,  and Cheresh DA. Integrins in cancer: biological implications and therapeutic opportunities. Nature Reviews Cancer 10, 9-22 (January 2010) | doi:10.1038/nrc2748&lt;br /&gt;
&lt;br /&gt;
[3]Dos Santos PB, Zanetti JS, Ribeiro-Silva A, Beltrão EIC. Beta 1 integrin predicts survival in breast cancer: a clinicopathological and immunohistochemical study. Diagn Pathol 7:104.(2012)&lt;br /&gt;
&lt;br /&gt;
[4] Barney LE, Dandley EC, Jansen LE, Reich NG, Mercurio AM, Peyton SR. “A Cell-ECM Screening Method to Predict Breast Cancer Metastasis”. (2014) In Review.&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065660</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065660"/>
		<updated>2014-11-19T20:19:13Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Cancer cell migration, Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Integrin Beta 1 and Alpha 5&#039; scene=&#039;60/609772/Integrinb1alpha5/1&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
Blue-Alpha 5 chain&lt;br /&gt;
Red-Beta 1 chain&lt;br /&gt;
Grey-SG/19 Fab fragment light chain&lt;br /&gt;
Green-SG/19 Fab fragment heavy chain&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extracellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including collagen, laminin and fibronectin.  Integrin adhesion to the extra cellular matrix is key for cell ability to adhere, migrate and proliferate in both 2D and 3D systems. These will eventually form adhesion complexes, which regulate actomyocin polymerization. During migration, cells continually form new focal adhesions at the leading edge of the cell and release adhesion complexes at the back of the cell, enabling forward movement.&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt; N-acetyl-D-glucosamine may regulate integrin signaling during cancer cell migration.[1]&lt;br /&gt;
&lt;br /&gt;
==Integrins and cancer==&lt;br /&gt;
&lt;br /&gt;
Integrins binding to the extracellular matrix provide cells the ability to migrate and remodel the surrounding microenvironment. For these reasons, integrins are extremely important in cancer metastasis, and the progression of solid tumors. When cells bind to extracellular matrix proteins, like &amp;lt;scene name=&#039;60/609772/Rgd_bound/1&#039;&amp;gt;RGD (black)&amp;lt;/scene&amp;gt; with integrins, these proteins can stimulate survival, migration/invasion, and proliferation  [2]. High expression of integrin beta 1 has been shown to drive primary tumor progression and metastasis, but targeting integrins for cancer treatment has seen limited success [3]. Likely, these failures stem from differential integrin expression between cancer cells, and new technologies to screen cancer cell populations are being developed to screen for affective therapies [4]. These technologies will likely allow for more selective treatment and better clinical efficacy for integrin inhibitors. &lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. &lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
[1] C. Saravanan, F. Liu, I.K. Gipson and N. Panjwani1. Galectin-3 promotes lamellipodia formation in epithelial cells by interacting with complex N-glycans on 31 integrin. Journal of Cell Science 122, 3684-3693 Published by The Company of Biologists (2009). doi:10.1242/jcs.045674.&lt;br /&gt;
&lt;br /&gt;
[2] Desgrossellier JS,  and Cheresh DA. Integrins in cancer: biological implications and therapeutic opportunities. Nature Reviews Cancer 10, 9-22 (January 2010) | doi:10.1038/nrc2748&lt;br /&gt;
&lt;br /&gt;
[3]Dos Santos PB, Zanetti JS, Ribeiro-Silva A, Beltrão EIC. Beta 1 integrin predicts survival in breast cancer: a clinicopathological and immunohistochemical study. Diagn Pathol 7:104.(2012)&lt;br /&gt;
&lt;br /&gt;
[4] Barney LE, Dandley EC, Jansen LE, Reich NG, Mercurio AM, Peyton SR. “A Cell-ECM Screening Method to Predict Breast Cancer Metastasis”. (2014) In Review.&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065659</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065659"/>
		<updated>2014-11-19T20:06:50Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Cancer cell migration, Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Integrin Beta 1 and Alpha 5&#039; scene=&#039;60/609772/Integrinb1alpha5/1&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
Blue-Alpha 5 chain&lt;br /&gt;
Red-Beta 1 chain&lt;br /&gt;
Grey-SG/19 Fab fragment light chain&lt;br /&gt;
Green-SG/19 Fab fragment heavy chain&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extracellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including collagen, laminin and fibronectin.  Integrin adhesion to the extra cellular matrix is key for cell ability to adhere, migrate and proliferate in both 2D and 3D systems. These will eventually form adhesion complexes, which regulate actomyocin polymerization. During migration, cells continually form new focal adhesions at the leading edge of the cell and release adhesion complexes at the back of the cell, enabling forward movement.&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt; N-acetyl-D-glucosamine may regulate integrin signaling during cancer cell migration.[1]&lt;br /&gt;
&lt;br /&gt;
==Integrins and cancer==&lt;br /&gt;
&lt;br /&gt;
Integrins binding to the extracellular matrix provide cells the ability to migrate and remodel the surrounding microenvironment. For these reasons, integrins are extremely important in cancer metastasis, and the progression of solid tumors. When cells bind to extracellular matrix proteins with integrins, these proteins can stimulate survival, migration/invasion, and proliferation  [2]. High expression of integrin beta 1 has been shown to drive primary tumor progression and metastasis, but targeting integrins for cancer treatment has seen limited success [3]. Likely, these failures stem from differential integrin expression between cancer cells, and new technologies to screen cancer cell populations are being developed to screen for affective therapies [4]. These technologies will likely allow for more selective treatment and better clinical efficacy for integrin inhibitors. &lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. &lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
[1] C. Saravanan, F. Liu, I.K. Gipson and N. Panjwani1. Galectin-3 promotes lamellipodia formation in epithelial cells by interacting with complex N-glycans on 31 integrin. Journal of Cell Science 122, 3684-3693 Published by The Company of Biologists (2009). doi:10.1242/jcs.045674.&lt;br /&gt;
&lt;br /&gt;
[2] Desgrossellier JS,  and Cheresh DA. Integrins in cancer: biological implications and therapeutic opportunities. Nature Reviews Cancer 10, 9-22 (January 2010) | doi:10.1038/nrc2748&lt;br /&gt;
&lt;br /&gt;
[3]Dos Santos PB, Zanetti JS, Ribeiro-Silva A, Beltrão EIC. Beta 1 integrin predicts survival in breast cancer: a clinicopathological and immunohistochemical study. Diagn Pathol 7:104.(2012)&lt;br /&gt;
&lt;br /&gt;
[4] Barney LE, Dandley EC, Jansen LE, Reich NG, Mercurio AM, Peyton SR. “A Cell-ECM Screening Method to Predict Breast Cancer Metastasis”. (2014) In Review.&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065658</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065658"/>
		<updated>2014-11-19T20:05:20Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Cancer cell migration, Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Integrin Beta 1 and Alpha 5&#039; scene=&#039;60/609772/Integrinb1alpha5/1&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extracellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including collagen, laminin and fibronectin.  Integrin adhesion to the extra cellular matrix is key for cell ability to adhere, migrate and proliferate in both 2D and 3D systems. These will eventually form adhesion complexes, which regulate actomyocin polymerization. During migration, cells continually form new focal adhesions at the leading edge of the cell and release adhesion complexes at the back of the cell, enabling forward movement.&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt; N-acetyl-D-glucosamine may regulate integrin signaling during cancer cell migration.[1]&lt;br /&gt;
&lt;br /&gt;
==Integrins and cancer==&lt;br /&gt;
&lt;br /&gt;
Integrins binding to the extracellular matrix provide cells the ability to migrate and remodel the surrounding microenvironment. For these reasons, integrins are extremely important in cancer metastasis, and the progression of solid tumors. When cells bind to extracellular matrix proteins with integrins, these proteins can stimulate survival, migration/invasion, and proliferation  [2]. High expression of integrin beta 1 has been shown to drive primary tumor progression and metastasis, but targeting integrins for cancer treatment has seen limited success [3]. Likely, these failures stem from differential integrin expression between cancer cells, and new technologies to screen cancer cell populations are being developed to screen for affective therapies [4]. These technologies will likely allow for more selective treatment and better clinical efficacy for integrin inhibitors. &lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. &lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
[1] C. Saravanan, F. Liu, I.K. Gipson and N. Panjwani1. Galectin-3 promotes lamellipodia formation in epithelial cells by interacting with complex N-glycans on 31 integrin. Journal of Cell Science 122, 3684-3693 Published by The Company of Biologists (2009). doi:10.1242/jcs.045674.&lt;br /&gt;
&lt;br /&gt;
[2] Desgrossellier JS,  and Cheresh DA. Integrins in cancer: biological implications and therapeutic opportunities. Nature Reviews Cancer 10, 9-22 (January 2010) | doi:10.1038/nrc2748&lt;br /&gt;
&lt;br /&gt;
[3]Dos Santos PB, Zanetti JS, Ribeiro-Silva A, Beltrão EIC. Beta 1 integrin predicts survival in breast cancer: a clinicopathological and immunohistochemical study. Diagn Pathol 7:104.(2012)&lt;br /&gt;
&lt;br /&gt;
[4] Barney LE, Dandley EC, Jansen LE, Reich NG, Mercurio AM, Peyton SR. “A Cell-ECM Screening Method to Predict Breast Cancer Metastasis”. (2014) In Review.&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065656</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065656"/>
		<updated>2014-11-19T19:43:35Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Cancer cell migration, Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extracellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including collagen, laminin and fibronectin.  Integrin adhesion to the extra cellular matrix is key for cell ability to adhere, migrate and proliferate in both 2D and 3D systems. These will eventually form adhesion complexes, which regulate actomyocin polymerization. During migration, cells continually form new focal adhesions at the leading edge of the cell and release adhesion complexes at the back of the cell, enabling forward movement.&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt; N-acetyl-D-glucosamine may regulate integrin signaling during cancer cell migration.[1]&lt;br /&gt;
&lt;br /&gt;
==Integrins and cancer==&lt;br /&gt;
&lt;br /&gt;
Integrins binding to the extracellular matrix provide cells the ability to migrate and remodel the surrounding microenvironment. For these reasons, integrins are extremely important in cancer metastasis, and the progression of solid tumors. When cells bind to extracellular matrix proteins with integrins, these proteins can stimulate survival, migration/invasion, and proliferation  [2]. High expression of integrin beta 1 has been shown to drive primary tumor progression and metastasis, but targeting integrins for cancer treatment has seen limited success [3]. Likely, these failures stem from differential integrin expression between cancer cells, and new technologies to screen cancer cell populations are being developed to screen for affective therapies [4]. These technologies will likely allow for more selective treatment and better clinical efficacy for integrin inhibitors. &lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. &lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
[1] C. Saravanan, F. Liu, I.K. Gipson and N. Panjwani1. Galectin-3 promotes lamellipodia formation in epithelial cells by interacting with complex N-glycans on 31 integrin. Journal of Cell Science 122, 3684-3693 Published by The Company of Biologists (2009). doi:10.1242/jcs.045674.&lt;br /&gt;
&lt;br /&gt;
[2] Desgrossellier JS,  and Cheresh DA. Integrins in cancer: biological implications and therapeutic opportunities. Nature Reviews Cancer 10, 9-22 (January 2010) | doi:10.1038/nrc2748&lt;br /&gt;
&lt;br /&gt;
[3]Dos Santos PB, Zanetti JS, Ribeiro-Silva A, Beltrão EIC. Beta 1 integrin predicts survival in breast cancer: a clinicopathological and immunohistochemical study. Diagn Pathol 7:104.(2012)&lt;br /&gt;
&lt;br /&gt;
[4] Barney LE, Dandley EC, Jansen LE, Reich NG, Mercurio AM, Peyton SR. “A Cell-ECM Screening Method to Predict Breast Cancer Metastasis”. (2014) In Review.&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065655</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065655"/>
		<updated>2014-11-19T19:41:06Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Cancer cell migration, Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extracellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including collagen, laminin and fibronectin.  Integrin adhesion to the extra cellular matrix is key for cell ability to adhere, migrate and proliferate in both 2D and 3D systems. These will eventually form adhesion complexes, which regulate actomyocin polymerization. During migration, cells continually form new focal adhesions at the leading edge of the cell and release adhesion complexes at the back of the cell, enabling forward movement.&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt; N-acetyl-D-glucosamine may regulate integrin signaling during cancer cell migration.[1]&lt;br /&gt;
&lt;br /&gt;
==Integrins and cancer==&lt;br /&gt;
&lt;br /&gt;
Integrins binding to the extracellular matrix provide cells the ability to migrate and remodel the surrounding extracellular matrix. For these reasons, integrins are extremely important in cancer metastasis, and the progression of solid tumors; which stiffen over time from ECM remodeling [2,3]. When cells bind to extracellular matrix proteins with integrins, these proteins can stimulate survival, migration/invasion, and proliferation. High expression of integrin beta 1 has been shown to drive primary tumor profession and metastasis, but targeting integrins for cancer treatment has seen limited success [4]. Likely, these failures stem from differential integrin expression between cancer cells, and new technologies to screen cancer cell populations are being developed to screen for affective therapies [5]. Hopefully these technologies will allow for more selective treatment and better clinical efficacy for integrin inhibitors. &lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. &lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
[1] C. Saravanan, F. Liu, I.K. Gipson and N. Panjwani1. Galectin-3 promotes lamellipodia formation in epithelial cells by interacting with complex N-glycans on 31 integrin. Journal of Cell Science 122, 3684-3693 Published by The Company of Biologists (2009). doi:10.1242/jcs.045674.&lt;br /&gt;
&lt;br /&gt;
[2] Desgrossellier JS,  and Cheresh DA. Integrins in cancer: biological implications and therapeutic opportunities. Nature Reviews Cancer 10, 9-22 (January 2010) | doi:10.1038/nrc2748&lt;br /&gt;
&lt;br /&gt;
[3] Oranto M, Sarrazy V, Bonte F, Hinz B, Gabbiani G, and Desmouliere A. The role of the myofibroblast in tumor stroma remodeling. Cell Adh Migr 6, 203-219 (2012)&lt;br /&gt;
&lt;br /&gt;
[4]Dos Santos PB, Zanetti JS, Ribeiro-Silva A, Beltrão EIC. Beta 1 integrin predicts survival in breast cancer: a clinicopathological and immunohistochemical study. Diagn Pathol 7:104.(2012)&lt;br /&gt;
&lt;br /&gt;
[5] Barney LE, Dandley EC, Jansen LE, Reich NG, Mercurio AM, Peyton SR. “A Cell-ECM Screening Method to Predict Breast Cancer Metastasis”. (2014) In Review.&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065654</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065654"/>
		<updated>2014-11-19T19:35:33Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Cancer cell migration, Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extracellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including collagen, laminin and fibronectin.  Integrin adhesion to the extra cellular matrix is key for cell ability to adhere, migrate and proliferate in both 2D and 3D systems. These will eventually form adhesion complexes, which regulate actomyocin polymerization. During migration, cells continually form new focal adhesions at the leading edge of the cell and release adhesion complexes at the back of the cell, enabling forward movement.&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt; N-acetyl-D-glucosamine may regulate integrin signaling during cancer cell migration.[1]&lt;br /&gt;
&lt;br /&gt;
==Integrins and cancer==&lt;br /&gt;
&lt;br /&gt;
Integrins binding to the extracellular matrix provide cells the ability to migrate and remodel the surrounding extracellular matrix. For these reasons, integrins are extremely important in cancer metastasis, and the progression of solid tumors; which stiffen over time from ECM remodeling [2,3]. When cells bind to extracellular matrix proteins with integrins, these proteins can stimulate survival, migration/invasion, and proliferation. Integrins are over expressed in cancer, but targeting integrins to treat cancer has seen limited success. Likely, these failures stem from differential integrin expression between cancer cells, and new technologies to screen cancer cell populations are being developed to screen for affective therapies [4]. Hopefully these technologies will allow for more selective treatment and better clinical efficacy for integrin inhibitors. &lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. &lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
[1] C. Saravanan, F. Liu, I.K. Gipson and N. Panjwani1. Galectin-3 promotes lamellipodia formation in epithelial cells by interacting with complex N-glycans on 31 integrin. Journal of Cell Science 122, 3684-3693 Published by The Company of Biologists (2009). doi:10.1242/jcs.045674.&lt;br /&gt;
&lt;br /&gt;
[2] Desgrossellier JS,  and Cheresh DA. Integrins in cancer: biological implications and therapeutic opportunities. Nature Reviews Cancer 10, 9-22 (January 2010) | doi:10.1038/nrc2748&lt;br /&gt;
&lt;br /&gt;
[3] Oranto M, Sarrazy V, Bonte F, Hinz B, Gabbiani G, and Desmouliere A. The role of the myofibroblast in tumor stroma remodeling. Cell Adh Migr 6, 203-219 (2012)&lt;br /&gt;
&lt;br /&gt;
[4] Barney LE, Dandley EC, Jansen LE, Reich NG, Mercurio AM, Peyton SR. “A Cell-ECM Screening Method to Predict Breast Cancer Metastasis”. (2014) In Review.&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065653</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065653"/>
		<updated>2014-11-19T19:31:20Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Cancer cell migration, Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extracellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including collagen, laminin and fibronectin.  Integrin adhesion to the extra cellular matrix is key for cell ability to adhere, migrate and proliferate in both 2D and 3D systems. These will eventually form adhesion complexes, which regulate actomyocin polymerization. During migration, cells continually form new focal adhesions at the leading edge of the cell and release adhesion complexes at the back of the cell, enabling forward movement.&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt; N-acetyl-D-glucosamine may regulate integrin signaling during cancer cell migration.[1]&lt;br /&gt;
&lt;br /&gt;
==Integrins and cancer==&lt;br /&gt;
&lt;br /&gt;
Integrins binding to the extracellular matrix provide cells the ability to migrate and remodel the surrounding extracellular matrix. For these reasons, integrins are extremely important in cancer metastasis, and the progression of solid tumors; which stiffen over time from ECM remodeling [2,3]. When cells bind to extracellular matrix proteins with integrins, these proteins can stimulate survival, migration/invasion, and proliferation. Integrins are over expressed in cancer, but targeting integrins to treat cancer has seen limited success. Likely, these failures stem from differential integrin expression between cancer cells, and new technologies to screen cancer cell populations are being developed to screen for affective therapies [4]. Hopefully these technologies will allow for more selective treatment and better clinical efficacy for integrin inhibitors. &lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. &lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
[1] C. Saravanan, F. Liu, I.K. Gipson and N. Panjwani1. Galectin-3 promotes lamellipodia formation in epithelial cells by interacting with complex N-glycans on 31 integrin. Journal of Cell Science 122, 3684-3693 Published by The Company of Biologists (2009). doi:10.1242/jcs.045674.&lt;br /&gt;
[2] JS. Desgrossellier and DA. Cheresh. Integrins in cancer: biological implications and therapeutic opportunities. Nature Reviews Cancer 10, 9-22 (January 2010) | doi:10.1038/nrc2748&lt;br /&gt;
[3] M. Oranto, V. Sarrazy, F. Bonte, B. Hinz, G. Gabbiani and A. Desmouliere. The role of the myofibroblast in tumor stroma remodeling. Cell Adh Migr 6, 203-219 (2012)&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065651</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065651"/>
		<updated>2014-11-19T19:12:25Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Cancer cell migration, Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extracellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including collagen, laminin and fibronectin.  Integrin adhesion to the extra cellular matrix is key for cell ability to adhere, migrate and proliferate in both 2D and 3D systems. These will eventually form adhesion complexes, which regulate actomyocin polymerization. During migration, cells continually form new focal adhesions at the leading edge of the cell and release adhesion complexes at the back of the cell, enabling forward movement.&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt; N-acetyl-D-glucosamine may regulate integrin signaling during cancer cell migration.[1]&lt;br /&gt;
&lt;br /&gt;
==Integrins and cancer==&lt;br /&gt;
&lt;br /&gt;
Integrins binding to the extracellular matrix provide cells with the traction to migrate and regulates their ability to remodel the extracellular matrix. For these reasons, integrins are extremely important in cancer metastasis, and the progression of solid tumors; which often stiffens from ECM remodeling [,]. When cells bind to extracellular matrix proteins with integrins, these proteins can stimulate survival, migration/invasion, and proliferation. Integrins are over expressed in cancer, but targeting integrins to treat cancer has seen limited success. Likely, these failures stem from differential integrin expression between cancer cells, and new technologies to screen cancer cell populations are being developed to screen for affective therapies []. Hopefully these technologies will allow for more selective treatment and better clinical efficacy for integrin inhibitors. &lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. &lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
[1] C. Saravanan, F. Liu, I.K. Gipson and N. Panjwani1. Galectin-3 promotes lamellipodia formation in epithelial cells by interacting with complex N-glycans on 31 integrin. Journal of Cell Science 122, 3684-3693 Published by The Company of Biologists (2009). doi:10.1242/jcs.045674.&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065649</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065649"/>
		<updated>2014-11-19T18:43:56Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt;&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extracellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including collagen, laminin and fibronectin. &lt;br /&gt;
&lt;br /&gt;
==Integrins and cancer==&lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. &lt;br /&gt;
&lt;br /&gt;
==References==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065648</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065648"/>
		<updated>2014-11-19T18:41:40Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt;&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extracellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including collagen, laminin and fibronectin. &lt;br /&gt;
&lt;br /&gt;
==Disease==&lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. &lt;br /&gt;
&lt;br /&gt;
==References==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065642</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065642"/>
		<updated>2014-11-19T18:15:39Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt;&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extra cellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including collagen, laminin and fibronectin. &lt;br /&gt;
&lt;br /&gt;
==Disease==&lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role in the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. &lt;br /&gt;
&lt;br /&gt;
==References==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065640</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065640"/>
		<updated>2014-11-19T18:15:11Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt;&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
Integrins are a class of surface proteins that bind to extra cellular matrix components and transmit chemical and mechanical cues to internal signaling pathways. Integrin beta 1 binds many proteins when dimerized with an alpha subunit, including collagen, laminin and fibronectin. &lt;br /&gt;
&lt;br /&gt;
==Disease==&lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix and how these interactions play a role the progression of cardiovascular disease and cancer. We aim to understand the downstream signaling pathways activated when cells use their integrins to bind to matrix and how this translates to the disease of interest. &lt;br /&gt;
&lt;br /&gt;
==References==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065606</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065606"/>
		<updated>2014-11-19T18:07:59Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt;&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
==Disease==&lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from the extracellular matrix, and how these interactions play a role in disease progression. By creating synthetic microenvironments, we are able to have tight control of cell-matirx interactions, allowing us to better understand how cells use their integrins to bind to matrix, and what downstream signaling pathways this binding sets off. &lt;br /&gt;
&lt;br /&gt;
==References==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065604</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065604"/>
		<updated>2014-11-19T18:07:38Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Here are the &amp;lt;scene name=&#039;60/609772/N-acetyl-d-glucosamine/2&#039;&amp;gt;N-acetyl-d-glucosamine locations!&amp;lt;/scene&amp;gt;&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
==Disease==&lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies how cells process chemical and physical cues from there extracellular matrix, and how these interactions play a role in disease progression. By creating synthetic microenvironments, we are able to have tight control of cell-matirx interactions, allowing us to better understand how cells use their integrins to bind to matrix, and what downstream signaling pathways this binding sets off. &lt;br /&gt;
&lt;br /&gt;
==References==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065568</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065568"/>
		<updated>2014-11-19T17:45:49Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
==Disease==&lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies ...&lt;br /&gt;
&lt;br /&gt;
==References==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065563</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065563"/>
		<updated>2014-11-19T17:44:25Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
==Integrin Beta 1==&lt;br /&gt;
&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
==Disease==&lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies ...&lt;br /&gt;
&lt;br /&gt;
==References==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065560</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065560"/>
		<updated>2014-11-19T17:43:50Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
==Integrin Beta 1==&lt;br /&gt;
&amp;lt;StructureSection load=&#039;3rec&#039; size=&#039;350&#039;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
==Disease==&lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies ...&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
==References==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065554</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065554"/>
		<updated>2014-11-19T17:42:53Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
==Integrin Beta 1==&lt;br /&gt;
&amp;lt;StructureSection load=&#039;3rec&#039; size=&#039;350&#039; &#039;&#039;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
==Disease==&lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies ...&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
==References==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065553</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065553"/>
		<updated>2014-11-19T17:42:19Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
==Integrin Beta 1==&lt;br /&gt;
&amp;lt;StructureSection load=&#039;3rec&#039; size=&#039;350&#039; side=&#039;right&#039; scene=&#039;&#039;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
==Disease==&lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies ...&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
==References==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065549</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065549"/>
		<updated>2014-11-19T17:41:47Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
==Your Heading Here (maybe something like &#039;Structure&#039;)==&lt;br /&gt;
&amp;lt;StructureSection load=&#039;3rec&#039; size=&#039;350&#039; side=&#039;right&#039; scene=&#039;&#039;&amp;gt;&lt;br /&gt;
==Integrin Beta 1==&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
==Disease==&lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies ...&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
==References==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065546</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065546"/>
		<updated>2014-11-19T17:40:31Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
==Integrin Beta 1==&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
==Disease==&lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
The [http://www.peytonlab.org/ Peyton lab] studies ...&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
==References==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065544</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065544"/>
		<updated>2014-11-19T17:39:42Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
==Integrin Beta 1==&lt;br /&gt;
&amp;lt;StructureSection load=&#039;3rec&#039; size=&#039;350&#039; side=&#039;right&#039; caption=&#039;Escherichia coli reca protein-bound DNA (PDB entry [[3rec]])&#039; scene=&#039;&#039;&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
==Disease==&lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
==References==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065541</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065541"/>
		<updated>2014-11-19T17:38:44Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;Structure load=&#039;3VI4&#039; size=&#039;350&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;Insert caption here&#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
==Integrin Beta 1==&lt;br /&gt;
&amp;lt;StructureSection load=&#039;3rec&#039; size=&#039;350&#039; side=&#039;right&#039; caption=&#039;Escherichia coli reca protein-bound DNA (PDB entry [[3rec]])&#039; scene=&#039;&#039;&amp;gt;==Structure==&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
==Disease==&lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;br /&gt;
&lt;br /&gt;
&amp;lt;/StructureSection&amp;gt;&lt;br /&gt;
==References==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=CBI_Molecules&amp;diff=2065523</id>
		<title>CBI Molecules</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=CBI_Molecules&amp;diff=2065523"/>
		<updated>2014-11-19T17:32:49Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;These are molecules under study by members of the [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program].&lt;br /&gt;
Many of the  molecules we study are featured at the [http://www.molecularplayground.org/ Molecular Playground] (see also [[Molecular Playground|Molecular Playground in Proteopedia]]). Follow the links below to read nontechnical descriptions, in Proteopedia, of these molecules.&lt;br /&gt;
&lt;br /&gt;
UMass CBI Members, add your molecules to the list (which is alphabetical by CBI research mentor); follow the instructions below the list.&lt;br /&gt;
&lt;br /&gt;
Fall 2014: CBI Molecules are due 12/3/14 and should be added at the TOP of the list from your lab. Label it as &amp;quot;in progress&amp;quot; until you are finished, and then as &amp;quot;New 2014&amp;quot; or &amp;quot;Revised 2014&amp;quot;. For those editing an existing CBI Molecule, start by making a copy of that entry (leaving the original intact) so that it retains the full author list of all authors that contributed (or include credits and a link to the original page and authors if it does not).&lt;br /&gt;
Follow the instructions at the bottom of this page.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Molecules==&lt;br /&gt;
&#039;&#039;&#039;** Designates CBI Molecules Featured on [http://www.umass.edu/cbi/ CBI website]&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
[http://chamberslab.com/wp/ Chambers Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Glutamate Receptor]]&#039;&#039;&#039;,  Amanda Hussey, Steve McCarron, Rosie Combs-Bachmann, Mariel Feliciano&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/~chenlab/index.HTML Chen Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/ClyA]]&#039;&#039;&#039;, Bib Yang&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/OmpG]]&#039;&#039;&#039;, Christina Chisholm&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://openwetware.org/wiki/Chien Chien Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Homo-dimeric RcdA]]&#039;&#039;&#039;, Kamal K. Joshi &lt;br /&gt;
: **&#039;&#039;&#039;[[Molecular Playground/Hexameric ClpX]]&#039;&#039;&#039;, Joanne Lau &#039;&#039;&#039;Best CBI Molecule 2011&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/DNA replication initiator DnaA]]&#039;&#039;&#039;, Jing Liu&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Farkas Lab&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Forbes Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CheR]]&#039;&#039;&#039;,  Miaomin Zhang&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/RBP]]&#039;&#039;&#039;,  Jan Panteli&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/TRAIL]]&#039;&#039;&#039;,  Charley Swofford&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.biochem.umass.edu/garman/index.html Garman Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Human Protective Protein Cathepsin A]]&#039;&#039;&#039;, Yadilette Rivera-Colon&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Human PPCA]]&#039;&#039;&#039;, Nilima Kolli&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/gieraschlab/ Gierasch Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[CRABP I ( Cellular Retinoic Acid Binding Protein )|Molecular Playground/CRABP I]]&#039;&#039;&#039;, Kristine Faye Pobre, Mylene Ferrolino,Mangai Periasamy  &#039;&#039;&#039;Best Overall CBI Molecule 2010&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CRABP I (Cellular Retinoic Acid Binding Protein)]]&#039;&#039;&#039;, Gustavo Elberto Epalza Sanchez&lt;br /&gt;
: **&#039;&#039;&#039;[[Molecular_Playground/DHFR]]&#039;&#039;&#039;, Karan Hingorani &#039;&#039;&#039;Best CBI Molecule 2012&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/jhardy/ Hardy Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Executioner Caspase-7]]&#039;&#039;&#039;, Derek MacPherson, Maureen E. Hill&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-3 Regulatory Mechanisms]]&#039;&#039;&#039;, Scott Eron, Bay Serrano, Yunlong Zhao&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-6 and neurodegeneration]]&#039;&#039;&#039;, Kevin Buadlart Dagbay&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-7 Dynamics]]&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-9 Regulation]]&#039;&#039;&#039;, Kristen Huber&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-6 (new)]]&#039;&#039;&#039;, Elih Velazquez&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Influenza A M2 transmembrane domain]]&#039;&#039;&#039;, Samantha Nicholls&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Dengue Virus Protease]]&#039;&#039;&#039;, Muslum Yildiz&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Hebert Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular_Playground/Hsp70-Hsp90]]&#039;&#039;&#039;,  Jill Graham&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular_Playground/ERDj5]]&#039;&#039;&#039;,  Lydia Lamriben&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Saposin C]]&#039;&#039;&#039;, Abla Tannous&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular_Playground/ERMan1]]&#039;&#039;&#039;,  Johan Sunryd&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.biochem.umass.edu/aheuck/aph.html Heuck Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular_Playground/Pcr H]]&#039;&#039;&#039;,  Fabian Romano, Carolina Morell-Pérez&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/mholden/ Holden Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Protective Antigen]]&#039;&#039;&#039;,  Jing Huang&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/people/kaltashovlab/ Kaltashov Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[http://proteopedia.org/wiki/index.php/Chengfeng_Ren Molecular Playground/Inteferon]&#039;&#039;&#039;, Chengfeng Ren&lt;br /&gt;
: &#039;&#039;&#039; [[Molecular Playground/Transferrin]]&#039;&#039;&#039;, Khaja Muneeruddin, Jake Pawlowski&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Velaglucerase]]&#039;&#039;&#039;, Adriana Kita&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Antithrombin-Heparin]]&#039;&#039;&#039;, Yunlong Zhao&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Knapp lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/FIH]]&#039;&#039;&#039;, Vanessa Chaplin, Cornelius Taabazuing, Breanne Holmes, John Hangasky&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Prolyl Hydroxylase Domain (PHD) Enzyme]]&#039;&#039;&#039;, Cristina Martin, Serap Pektas &#039;&#039;&#039;Best CBI Molecule Proteopedia Page 2010&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/mmaroney/ Maroney Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Nickel Superoxide Dismutase]]&#039;&#039;&#039;, Carolyn Carr&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CsoR and RcnR]]&#039;&#039;&#039;, Heidi Hu, Carolyn Carr&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/HypA]]&#039;&#039;&#039;, Heidi Hu&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/~cmartin/ Martin Lab]&lt;br /&gt;
&lt;br /&gt;
: **&#039;&#039;&#039;[[Molecular Playground/T7 RNAP Conformations]]&#039;&#039;&#039;, Luis E. Ramirez-Tapia &#039;&#039;&#039;Best CBI Molecule 2011&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/T7 RNA Polymerase (7 mer int)]]&#039;&#039;&#039;, Ankit Vahia&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Human mtRNA pol]]&#039;&#039;&#039;, Ketan Mathavan &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.peytonlab.org/ Peyton Lab]&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/IntegrinBeta1]]&#039;&#039;&#039;, Lauren Jansen, Lauren Barney, Elizabeth Brooks, Alyssa Schwartz ***&#039;&#039;&#039;NEW FALL 2014&#039;&#039;&#039;&#039;***&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/MMP14]]&#039;&#039;&#039;, Lauren Jansen&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/C-Raf]]&#039;&#039;&#039;, Thuy Nguyen&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/FAK]]&#039;&#039;&#039;, Dannielle Ryman&lt;br /&gt;
&lt;br /&gt;
[http://roberts.openwetware.org/ Roberts Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Taxol]]&#039;&#039;&#039;,  Rohan Patil, Sarah Wilson&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Insulin]]&#039;&#039;&#039;, Whitney Stoppel&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.umass.edu/rotellogroup/ Rotello Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Reverse transcriptase|Molecular Playground/Reverse Transcriptase]]&#039;&#039;&#039;, Daniel Moyano-Marino&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Pancreatic Lipase]]&#039;&#039;&#039;,  Rui Tang&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular playground/Chymotrypsin]]&#039;&#039;&#039;,  Brad&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Targeting Peptide]]&#039;&#039;&#039;, David Solfiell&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://http://www.umass.edu/schiffman/  Schiffman Lab]&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Streptavidin]]&#039;&#039;&#039;, Katrina Rieger&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.biochem.umass.edu/faculty/danny-j-schnell Schnell Lab]&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Tic40]]&#039;&#039;&#039;, Mine Canakci&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Tew Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/HIV Tat]]&#039;&#039;&#039;, Brittany deRonde&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Thayumanavan Lab&lt;br /&gt;
: &#039;&#039;&#039;[[Interleukin-1 beta]]&#039;&#039;&#039;, Huan He&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Lysozyme ]]&#039;&#039;&#039;, Daniella Gonzalez&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Beta-galactosidase]]&#039;&#039;&#039;, Judy Ventura&lt;br /&gt;
: &#039;&#039;&#039;[[User:Krishna Reddy Ragupathi|Molecular Playground/Carbonic Anhydrase]]&#039;&#039;&#039;, Krishna Reddy Raghupathi&lt;br /&gt;
: &#039;&#039;&#039;[[User:Rami Rajasekhar Reddy|Molecular Playground/Avidin]]&#039;&#039;&#039;, Rami Rajasekar Reddy&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Biotin binding avidin]]&#039;&#039;&#039;, Diego Amado &lt;br /&gt;
: &#039;&#039;&#039;[[User:Jiaming Zhuang|Molecular Playground/MMP12]]&#039;&#039;&#039;, Jiaming Zhuang&lt;br /&gt;
: &#039;&#039;&#039; [[User:Jing Guo|Molecular Playground/Gluconase]]&#039;&#039;&#039;, Jing Guo&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Glutathione Reductase]]&#039;&#039;&#039;, Reuben Chacko&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Thayumanavan &amp;amp; Vachet Labs&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Trypsin]]&#039;&#039;&#039;, Gladys Murage&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/thompson/index.html Thompson Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Bacterial Chemotaxis Complex]]&#039;&#039;&#039;, Elizabeth R. Haglin, Maryam Kashefi&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CheA]]&#039;&#039;&#039;, Elizabeth R. Haglin&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Bacterial Chemotaxis Receptors]]&#039;&#039;&#039;, Lynmarie K. Thompson, Shiela M. Jones&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Cytoplasmic domain of chemoreceptor of Thermotoga maritima]]&#039;&#039;&#039;,  Xuni Li&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/~vachet/index.html Vachet Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;[[Molecular Playground/Human Serum Albumin]]&#039;&#039;&#039;, Mahalia Serrano&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular playground/beta 2 microglobulin]]&#039;&#039;&#039;,  Nick Borotto &#039;&#039;&#039;Best CBI Molecule Jmol scenes 2010&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Myoglobin]]&#039;&#039;&#039;,  Yuping Zhou &lt;br /&gt;
:&#039;&#039;&#039;[[Molecular Playground/ Copper-Zinc Superoxide Dismutase]]&#039;&#039;&#039;, Shaynah Browne&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Ubiquitin salt bridge discussion]]&#039;&#039;&#039;, Zhe Zhang&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Other Molecules of interest&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/PcrA Helicase]]&#039;&#039;&#039;, Luis E Ramirez-Tapia, [http://www.chem.umass.edu/~cmartin/ Martin Lab]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Other Laboratories&lt;br /&gt;
&lt;br /&gt;
:&#039;&#039;&#039;[[Molecular Playground/4&#039;-PHOSPHOPANTETHEINYL TRANSFERASE (Sfp)]]&#039;&#039;&#039;, Jon Amoroso, Gitanjeli Prasad, Lawrence Sheringham Borketey, Schnarr lab&lt;br /&gt;
: &#039;&#039;&#039;[[6-deoxyerythronolide_B_synthase_(DEBS)|Molecular Playground/6-Deoxyerythronolide B Synthase]]&#039;&#039;&#039;, Tsung-Yi Lin, Jon Amoroso, Lawrence Sheringham Borketey, Schnarr lab&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/ACP apo]]&#039;&#039;&#039;, Gitanjeli Prasad,  Schnarr lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/cytoplasmic domain of a serine chemotaxis receptor]]&#039;&#039;&#039;,  Meili Yang, Weis lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Alginate-Fall2011]]&#039;&#039;&#039;, Joe White, David Griffi, Bhatia Lab&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Poly(ethylene glycol)]]&#039;&#039;&#039;, Erika M. Saffer, Bhatia Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/YKL-40]]&#039;&#039;&#039;, Ralph A. Francescone III, [http://www.bio.umass.edu/mcb/faculty/Shao.html Shao Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/BLG|Molecular Playground/β-lactoglobulin]]&#039;&#039;&#039;, Daniel Seeman, Dubin Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/ADAM13]]&#039;&#039;&#039;, Genevieve Abbruzzese, Alfandari Lab&lt;br /&gt;
&lt;br /&gt;
==Instructions==&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;The goal is for students to work collaboratively to create one excellent CBI Molecule for each CBI research group, to be featured on the CBI website.&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Fall 2014: Complete steps 1-3 before the CBI Molecule Workshop on 11/19; bring your computer to the CBI Molecule Workshop in ISB 321. You will be able to start work on your CBI Molecule at the workshop. You should plan to stay and finish your molecule after the workshop (or as soon as possible) while the instructions and ideas are fresh in your mind.&lt;br /&gt;
&lt;br /&gt;
A successful CBI Molecule is an interesting, nontechnical description of a molecule related to your group&#039;s research. It should tell an interesting story with few words and many green scenes. Green scenes should be clear and attractive illustrations that tell your story. It&#039;s great if you can end with a brief statement about how it relates to your group&#039;s research goals.&lt;br /&gt;
&lt;br /&gt;
1. If you don&#039;t already have one, request a Proteopedia account and log in. &lt;br /&gt;
&lt;br /&gt;
2. Read through the rest of the instructions, do the tutorials below, and look at any existing CBI Molecules from your research group. Talk with other CBI students in your research group and decide how you will collaborate to make an improved CBI Molecule related to your group&#039;s research. Develop ideas for the scenes that each of you will make.&lt;br /&gt;
&lt;br /&gt;
3. Get started working in Proteopedia. Make yourself a sandbox page: Enter &amp;quot;User:Your Name/Sandbox 1&amp;quot; (omit quotes) in the search box, then follow instructions to edit this page. Practice entering text, inserting a structure window with scrolling text (green 4-square button on the right), and creating a green scene. Explore the HELP links below to learn how to make a green scene. You can look at other Proteopedia pages in edit mode to see how different effects (like colored text) are achieved (but this won&#039;t show you how the scene effects are made). &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Complete the above steps before the CBI Molecule Workshop.&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
4. When editing an existing CBI Molecule, leave the original intact and make a copy that you will edit so that it retains the full author list of all authors that contributed. You are encouraged to collaborate on the CBI Molecules, but everyone will need to log in as themself and create a green scene to get credit for their work and to appear as authors on the final list. If you are the sole student from your group enrolled in Chalk Talk and have not previously made a CBI Molecule, try to convince another group member who has previously made a CBI Molecule (see  list above) to join us for the workshop so that you can work together.&lt;br /&gt;
&lt;br /&gt;
5. Your final pages should be called &amp;quot;Molecular Playground/your molecule&amp;quot; and should have links on this CBI Molecule page -- put the new ones first on the list from your research group. Label them &amp;quot;in progress&amp;quot; until you are finished, and then &amp;quot;new 2014&amp;quot; or &amp;quot;revised 2014&amp;quot;. Minimize text; tell your story with green scenes!&lt;br /&gt;
&lt;br /&gt;
6. When your CBI Molecule is complete, send Lynmarie an email to nominate a cool scene/clever caption you would like to feature at the Molecular Playground (include a link to your CBI Molecule, name of the green scene, and caption).&lt;br /&gt;
&lt;br /&gt;
==Links to HELP pages==&lt;br /&gt;
Overview at [[Help:Contents ]]&lt;br /&gt;
&lt;br /&gt;
See also [[Help:Getting_Started_in_Proteopedia]] &lt;br /&gt;
&lt;br /&gt;
Videos showing how to use Proteopedia:&lt;br /&gt;
[[Proteopedia:Video_Guide]]&lt;br /&gt;
(Sometimes slow -- if you pause the video and wait awhile it will download and then you can play it without interruptions)&lt;br /&gt;
&lt;br /&gt;
[[Proteopedia:DIY:Scenes|Proteopedia Scenes: Do It Yourself]]&lt;br /&gt;
gives succinct step by step instructions on how to create a molecular scene.&lt;br /&gt;
&lt;br /&gt;
A powerpoint-like set of slides that walks a user through the process of creating a new page and a new molecular scene/green link.&lt;br /&gt;
[http://www.proteopedia.org/wiki/images/1/1b/2009_07_13_Proteopedia_Workshop.pdf Proteopedia Workshop Slides]&lt;br /&gt;
&lt;br /&gt;
[[Proteopedia:Guidelines for Ethical Writing]].&lt;br /&gt;
Please pay attention to the section about images. There are links to examples of images re-used with explicit permission.&lt;br /&gt;
&lt;br /&gt;
For other help resources, click on [[Help:Contents|Help]] in the &#039;&#039;navigation&#039;&#039; box at the upper left of every page in Proteopedia.&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=CBI_Molecules&amp;diff=2065511</id>
		<title>CBI Molecules</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=CBI_Molecules&amp;diff=2065511"/>
		<updated>2014-11-19T17:31:23Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;These are molecules under study by members of the [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program].&lt;br /&gt;
Many of the  molecules we study are featured at the [http://www.molecularplayground.org/ Molecular Playground] (see also [[Molecular Playground|Molecular Playground in Proteopedia]]). Follow the links below to read nontechnical descriptions, in Proteopedia, of these molecules.&lt;br /&gt;
&lt;br /&gt;
UMass CBI Members, add your molecules to the list (which is alphabetical by CBI research mentor); follow the instructions below the list.&lt;br /&gt;
&lt;br /&gt;
Fall 2014: CBI Molecules are due 12/3/14 and should be added at the TOP of the list from your lab. Label it as &amp;quot;in progress&amp;quot; until you are finished, and then as &amp;quot;New 2014&amp;quot; or &amp;quot;Revised 2014&amp;quot;. For those editing an existing CBI Molecule, start by making a copy of that entry (leaving the original intact) so that it retains the full author list of all authors that contributed (or include credits and a link to the original page and authors if it does not).&lt;br /&gt;
Follow the instructions at the bottom of this page.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Molecules==&lt;br /&gt;
&#039;&#039;&#039;** Designates CBI Molecules Featured on [http://www.umass.edu/cbi/ CBI website]&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
[http://chamberslab.com/wp/ Chambers Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Glutamate Receptor]]&#039;&#039;&#039;,  Amanda Hussey, Steve McCarron, Rosie Combs-Bachmann, Mariel Feliciano&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/~chenlab/index.HTML Chen Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/ClyA]]&#039;&#039;&#039;, Bib Yang&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/OmpG]]&#039;&#039;&#039;, Christina Chisholm&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://openwetware.org/wiki/Chien Chien Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Homo-dimeric RcdA]]&#039;&#039;&#039;, Kamal K. Joshi &lt;br /&gt;
: **&#039;&#039;&#039;[[Molecular Playground/Hexameric ClpX]]&#039;&#039;&#039;, Joanne Lau &#039;&#039;&#039;Best CBI Molecule 2011&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/DNA replication initiator DnaA]]&#039;&#039;&#039;, Jing Liu&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Farkas Lab&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Forbes Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CheR]]&#039;&#039;&#039;,  Miaomin Zhang&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/RBP]]&#039;&#039;&#039;,  Jan Panteli&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/TRAIL]]&#039;&#039;&#039;,  Charley Swofford&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.biochem.umass.edu/garman/index.html Garman Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Human Protective Protein Cathepsin A]]&#039;&#039;&#039;, Yadilette Rivera-Colon&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Human PPCA]]&#039;&#039;&#039;, Nilima Kolli&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/gieraschlab/ Gierasch Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[CRABP I ( Cellular Retinoic Acid Binding Protein )|Molecular Playground/CRABP I]]&#039;&#039;&#039;, Kristine Faye Pobre, Mylene Ferrolino,Mangai Periasamy  &#039;&#039;&#039;Best Overall CBI Molecule 2010&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CRABP I (Cellular Retinoic Acid Binding Protein)]]&#039;&#039;&#039;, Gustavo Elberto Epalza Sanchez&lt;br /&gt;
: **&#039;&#039;&#039;[[Molecular_Playground/DHFR]]&#039;&#039;&#039;, Karan Hingorani &#039;&#039;&#039;Best CBI Molecule 2012&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/jhardy/ Hardy Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Executioner Caspase-7]]&#039;&#039;&#039;, Derek MacPherson, Maureen E. Hill&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-3 Regulatory Mechanisms]]&#039;&#039;&#039;, Scott Eron, Bay Serrano, Yunlong Zhao&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-6 and neurodegeneration]]&#039;&#039;&#039;, Kevin Buadlart Dagbay&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-7 Dynamics]]&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-9 Regulation]]&#039;&#039;&#039;, Kristen Huber&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-6 (new)]]&#039;&#039;&#039;, Elih Velazquez&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Influenza A M2 transmembrane domain]]&#039;&#039;&#039;, Samantha Nicholls&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Dengue Virus Protease]]&#039;&#039;&#039;, Muslum Yildiz&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Hebert Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular_Playground/Hsp70-Hsp90]]&#039;&#039;&#039;,  Jill Graham&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular_Playground/ERDj5]]&#039;&#039;&#039;,  Lydia Lamriben&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Saposin C]]&#039;&#039;&#039;, Abla Tannous&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular_Playground/ERMan1]]&#039;&#039;&#039;,  Johan Sunryd&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.biochem.umass.edu/aheuck/aph.html Heuck Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular_Playground/Pcr H]]&#039;&#039;&#039;,  Fabian Romano, Carolina Morell-Pérez&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/mholden/ Holden Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Protective Antigen]]&#039;&#039;&#039;,  Jing Huang&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/people/kaltashovlab/ Kaltashov Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[http://proteopedia.org/wiki/index.php/Chengfeng_Ren Molecular Playground/Inteferon]&#039;&#039;&#039;, Chengfeng Ren&lt;br /&gt;
: &#039;&#039;&#039; [[Molecular Playground/Transferrin]]&#039;&#039;&#039;, Khaja Muneeruddin, Jake Pawlowski&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Velaglucerase]]&#039;&#039;&#039;, Adriana Kita&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Antithrombin-Heparin]]&#039;&#039;&#039;, Yunlong Zhao&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Knapp lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/FIH]]&#039;&#039;&#039;, Vanessa Chaplin, Cornelius Taabazuing, Breanne Holmes, John Hangasky&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Prolyl Hydroxylase Domain (PHD) Enzyme]]&#039;&#039;&#039;, Cristina Martin, Serap Pektas &#039;&#039;&#039;Best CBI Molecule Proteopedia Page 2010&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/mmaroney/ Maroney Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Nickel Superoxide Dismutase]]&#039;&#039;&#039;, Carolyn Carr&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CsoR and RcnR]]&#039;&#039;&#039;, Heidi Hu, Carolyn Carr&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/HypA]]&#039;&#039;&#039;, Heidi Hu&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/~cmartin/ Martin Lab]&lt;br /&gt;
&lt;br /&gt;
: **&#039;&#039;&#039;[[Molecular Playground/T7 RNAP Conformations]]&#039;&#039;&#039;, Luis E. Ramirez-Tapia &#039;&#039;&#039;Best CBI Molecule 2011&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/T7 RNA Polymerase (7 mer int)]]&#039;&#039;&#039;, Ankit Vahia&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Human mtRNA pol]]&#039;&#039;&#039;, Ketan Mathavan &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.peytonlab.org/ Peyton Lab]&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/IntegrinBeta1]]&#039;&#039;&#039;, Lauren Jansen, Lauren Barney, Elizabeth Brooks, Alyssa Schwartz&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/MMP14]]&#039;&#039;&#039;, Lauren Jansen&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/C-Raf]]&#039;&#039;&#039;, Thuy Nguyen&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/FAK]]&#039;&#039;&#039;, Dannielle Ryman&lt;br /&gt;
&lt;br /&gt;
[http://roberts.openwetware.org/ Roberts Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Taxol]]&#039;&#039;&#039;,  Rohan Patil, Sarah Wilson&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Insulin]]&#039;&#039;&#039;, Whitney Stoppel&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.umass.edu/rotellogroup/ Rotello Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Reverse transcriptase|Molecular Playground/Reverse Transcriptase]]&#039;&#039;&#039;, Daniel Moyano-Marino&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Pancreatic Lipase]]&#039;&#039;&#039;,  Rui Tang&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular playground/Chymotrypsin]]&#039;&#039;&#039;,  Brad&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Targeting Peptide]]&#039;&#039;&#039;, David Solfiell&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://http://www.umass.edu/schiffman/  Schiffman Lab]&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Streptavidin]]&#039;&#039;&#039;, Katrina Rieger&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.biochem.umass.edu/faculty/danny-j-schnell Schnell Lab]&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Tic40]]&#039;&#039;&#039;, Mine Canakci&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Tew Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/HIV Tat]]&#039;&#039;&#039;, Brittany deRonde&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Thayumanavan Lab&lt;br /&gt;
: &#039;&#039;&#039;[[Interleukin-1 beta]]&#039;&#039;&#039;, Huan He&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Lysozyme ]]&#039;&#039;&#039;, Daniella Gonzalez&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Beta-galactosidase]]&#039;&#039;&#039;, Judy Ventura&lt;br /&gt;
: &#039;&#039;&#039;[[User:Krishna Reddy Ragupathi|Molecular Playground/Carbonic Anhydrase]]&#039;&#039;&#039;, Krishna Reddy Raghupathi&lt;br /&gt;
: &#039;&#039;&#039;[[User:Rami Rajasekhar Reddy|Molecular Playground/Avidin]]&#039;&#039;&#039;, Rami Rajasekar Reddy&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Biotin binding avidin]]&#039;&#039;&#039;, Diego Amado &lt;br /&gt;
: &#039;&#039;&#039;[[User:Jiaming Zhuang|Molecular Playground/MMP12]]&#039;&#039;&#039;, Jiaming Zhuang&lt;br /&gt;
: &#039;&#039;&#039; [[User:Jing Guo|Molecular Playground/Gluconase]]&#039;&#039;&#039;, Jing Guo&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Glutathione Reductase]]&#039;&#039;&#039;, Reuben Chacko&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Thayumanavan &amp;amp; Vachet Labs&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Trypsin]]&#039;&#039;&#039;, Gladys Murage&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/thompson/index.html Thompson Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Bacterial Chemotaxis Complex]]&#039;&#039;&#039;, Elizabeth R. Haglin, Maryam Kashefi&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CheA]]&#039;&#039;&#039;, Elizabeth R. Haglin&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Bacterial Chemotaxis Receptors]]&#039;&#039;&#039;, Lynmarie K. Thompson, Shiela M. Jones&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Cytoplasmic domain of chemoreceptor of Thermotoga maritima]]&#039;&#039;&#039;,  Xuni Li&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/~vachet/index.html Vachet Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;[[Molecular Playground/Human Serum Albumin]]&#039;&#039;&#039;, Mahalia Serrano&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular playground/beta 2 microglobulin]]&#039;&#039;&#039;,  Nick Borotto &#039;&#039;&#039;Best CBI Molecule Jmol scenes 2010&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Myoglobin]]&#039;&#039;&#039;,  Yuping Zhou &lt;br /&gt;
:&#039;&#039;&#039;[[Molecular Playground/ Copper-Zinc Superoxide Dismutase]]&#039;&#039;&#039;, Shaynah Browne&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Ubiquitin salt bridge discussion]]&#039;&#039;&#039;, Zhe Zhang&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Other Molecules of interest&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/PcrA Helicase]]&#039;&#039;&#039;, Luis E Ramirez-Tapia, [http://www.chem.umass.edu/~cmartin/ Martin Lab]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Other Laboratories&lt;br /&gt;
&lt;br /&gt;
:&#039;&#039;&#039;[[Molecular Playground/4&#039;-PHOSPHOPANTETHEINYL TRANSFERASE (Sfp)]]&#039;&#039;&#039;, Jon Amoroso, Gitanjeli Prasad, Lawrence Sheringham Borketey, Schnarr lab&lt;br /&gt;
: &#039;&#039;&#039;[[6-deoxyerythronolide_B_synthase_(DEBS)|Molecular Playground/6-Deoxyerythronolide B Synthase]]&#039;&#039;&#039;, Tsung-Yi Lin, Jon Amoroso, Lawrence Sheringham Borketey, Schnarr lab&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/ACP apo]]&#039;&#039;&#039;, Gitanjeli Prasad,  Schnarr lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/cytoplasmic domain of a serine chemotaxis receptor]]&#039;&#039;&#039;,  Meili Yang, Weis lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Alginate-Fall2011]]&#039;&#039;&#039;, Joe White, David Griffi, Bhatia Lab&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Poly(ethylene glycol)]]&#039;&#039;&#039;, Erika M. Saffer, Bhatia Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/YKL-40]]&#039;&#039;&#039;, Ralph A. Francescone III, [http://www.bio.umass.edu/mcb/faculty/Shao.html Shao Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/BLG|Molecular Playground/β-lactoglobulin]]&#039;&#039;&#039;, Daniel Seeman, Dubin Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/ADAM13]]&#039;&#039;&#039;, Genevieve Abbruzzese, Alfandari Lab&lt;br /&gt;
&lt;br /&gt;
==Instructions==&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;The goal is for students to work collaboratively to create one excellent CBI Molecule for each CBI research group, to be featured on the CBI website.&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Fall 2014: Complete steps 1-3 before the CBI Molecule Workshop on 11/19; bring your computer to the CBI Molecule Workshop in ISB 321. You will be able to start work on your CBI Molecule at the workshop. You should plan to stay and finish your molecule after the workshop (or as soon as possible) while the instructions and ideas are fresh in your mind.&lt;br /&gt;
&lt;br /&gt;
A successful CBI Molecule is an interesting, nontechnical description of a molecule related to your group&#039;s research. It should tell an interesting story with few words and many green scenes. Green scenes should be clear and attractive illustrations that tell your story. It&#039;s great if you can end with a brief statement about how it relates to your group&#039;s research goals.&lt;br /&gt;
&lt;br /&gt;
1. If you don&#039;t already have one, request a Proteopedia account and log in. &lt;br /&gt;
&lt;br /&gt;
2. Read through the rest of the instructions, do the tutorials below, and look at any existing CBI Molecules from your research group. Talk with other CBI students in your research group and decide how you will collaborate to make an improved CBI Molecule related to your group&#039;s research. Develop ideas for the scenes that each of you will make.&lt;br /&gt;
&lt;br /&gt;
3. Get started working in Proteopedia. Make yourself a sandbox page: Enter &amp;quot;User:Your Name/Sandbox 1&amp;quot; (omit quotes) in the search box, then follow instructions to edit this page. Practice entering text, inserting a structure window with scrolling text (green 4-square button on the right), and creating a green scene. Explore the HELP links below to learn how to make a green scene. You can look at other Proteopedia pages in edit mode to see how different effects (like colored text) are achieved (but this won&#039;t show you how the scene effects are made). &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Complete the above steps before the CBI Molecule Workshop.&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
4. When editing an existing CBI Molecule, leave the original intact and make a copy that you will edit so that it retains the full author list of all authors that contributed. You are encouraged to collaborate on the CBI Molecules, but everyone will need to log in as themself and create a green scene to get credit for their work and to appear as authors on the final list. If you are the sole student from your group enrolled in Chalk Talk and have not previously made a CBI Molecule, try to convince another group member who has previously made a CBI Molecule (see  list above) to join us for the workshop so that you can work together.&lt;br /&gt;
&lt;br /&gt;
5. Your final pages should be called &amp;quot;Molecular Playground/your molecule&amp;quot; and should have links on this CBI Molecule page -- put the new ones first on the list from your research group. Label them &amp;quot;in progress&amp;quot; until you are finished, and then &amp;quot;new 2014&amp;quot; or &amp;quot;revised 2014&amp;quot;. Minimize text; tell your story with green scenes!&lt;br /&gt;
&lt;br /&gt;
6. When your CBI Molecule is complete, send Lynmarie an email to nominate a cool scene/clever caption you would like to feature at the Molecular Playground (include a link to your CBI Molecule, name of the green scene, and caption).&lt;br /&gt;
&lt;br /&gt;
==Links to HELP pages==&lt;br /&gt;
Overview at [[Help:Contents ]]&lt;br /&gt;
&lt;br /&gt;
See also [[Help:Getting_Started_in_Proteopedia]] &lt;br /&gt;
&lt;br /&gt;
Videos showing how to use Proteopedia:&lt;br /&gt;
[[Proteopedia:Video_Guide]]&lt;br /&gt;
(Sometimes slow -- if you pause the video and wait awhile it will download and then you can play it without interruptions)&lt;br /&gt;
&lt;br /&gt;
[[Proteopedia:DIY:Scenes|Proteopedia Scenes: Do It Yourself]]&lt;br /&gt;
gives succinct step by step instructions on how to create a molecular scene.&lt;br /&gt;
&lt;br /&gt;
A powerpoint-like set of slides that walks a user through the process of creating a new page and a new molecular scene/green link.&lt;br /&gt;
[http://www.proteopedia.org/wiki/images/1/1b/2009_07_13_Proteopedia_Workshop.pdf Proteopedia Workshop Slides]&lt;br /&gt;
&lt;br /&gt;
[[Proteopedia:Guidelines for Ethical Writing]].&lt;br /&gt;
Please pay attention to the section about images. There are links to examples of images re-used with explicit permission.&lt;br /&gt;
&lt;br /&gt;
For other help resources, click on [[Help:Contents|Help]] in the &#039;&#039;navigation&#039;&#039; box at the upper left of every page in Proteopedia.&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=CBI_Molecules&amp;diff=2065506</id>
		<title>CBI Molecules</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=CBI_Molecules&amp;diff=2065506"/>
		<updated>2014-11-19T17:30:25Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;These are molecules under study by members of the [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program].&lt;br /&gt;
Many of the  molecules we study are featured at the [http://www.molecularplayground.org/ Molecular Playground] (see also [[Molecular Playground|Molecular Playground in Proteopedia]]). Follow the links below to read nontechnical descriptions, in Proteopedia, of these molecules.&lt;br /&gt;
&lt;br /&gt;
UMass CBI Members, add your molecules to the list (which is alphabetical by CBI research mentor); follow the instructions below the list.&lt;br /&gt;
&lt;br /&gt;
Fall 2014: CBI Molecules are due 12/3/14 and should be added at the TOP of the list from your lab. Label it as &amp;quot;in progress&amp;quot; until you are finished, and then as &amp;quot;New 2014&amp;quot; or &amp;quot;Revised 2014&amp;quot;. For those editing an existing CBI Molecule, start by making a copy of that entry (leaving the original intact) so that it retains the full author list of all authors that contributed (or include credits and a link to the original page and authors if it does not).&lt;br /&gt;
Follow the instructions at the bottom of this page.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Molecules==&lt;br /&gt;
&#039;&#039;&#039;** Designates CBI Molecules Featured on [http://www.umass.edu/cbi/ CBI website]&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
[http://chamberslab.com/wp/ Chambers Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Glutamate Receptor]]&#039;&#039;&#039;,  Amanda Hussey, Steve McCarron, Rosie Combs-Bachmann, Mariel Feliciano&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/~chenlab/index.HTML Chen Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/ClyA]]&#039;&#039;&#039;, Bib Yang&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/OmpG]]&#039;&#039;&#039;, Christina Chisholm&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://openwetware.org/wiki/Chien Chien Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Homo-dimeric RcdA]]&#039;&#039;&#039;, Kamal K. Joshi &lt;br /&gt;
: **&#039;&#039;&#039;[[Molecular Playground/Hexameric ClpX]]&#039;&#039;&#039;, Joanne Lau &#039;&#039;&#039;Best CBI Molecule 2011&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/DNA replication initiator DnaA]]&#039;&#039;&#039;, Jing Liu&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Farkas Lab&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Forbes Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CheR]]&#039;&#039;&#039;,  Miaomin Zhang&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/RBP]]&#039;&#039;&#039;,  Jan Panteli&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/TRAIL]]&#039;&#039;&#039;,  Charley Swofford&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.biochem.umass.edu/garman/index.html Garman Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Human Protective Protein Cathepsin A]]&#039;&#039;&#039;, Yadilette Rivera-Colon&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Human PPCA]]&#039;&#039;&#039;, Nilima Kolli&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/gieraschlab/ Gierasch Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[CRABP I ( Cellular Retinoic Acid Binding Protein )|Molecular Playground/CRABP I]]&#039;&#039;&#039;, Kristine Faye Pobre, Mylene Ferrolino,Mangai Periasamy  &#039;&#039;&#039;Best Overall CBI Molecule 2010&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CRABP I (Cellular Retinoic Acid Binding Protein)]]&#039;&#039;&#039;, Gustavo Elberto Epalza Sanchez&lt;br /&gt;
: **&#039;&#039;&#039;[[Molecular_Playground/DHFR]]&#039;&#039;&#039;, Karan Hingorani &#039;&#039;&#039;Best CBI Molecule 2012&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/jhardy/ Hardy Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Executioner Caspase-7]]&#039;&#039;&#039;, Derek MacPherson, Maureen E. Hill&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-3 Regulatory Mechanisms]]&#039;&#039;&#039;, Scott Eron, Bay Serrano, Yunlong Zhao&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-6 and neurodegeneration]]&#039;&#039;&#039;, Kevin Buadlart Dagbay&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-7 Dynamics]]&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-9 Regulation]]&#039;&#039;&#039;, Kristen Huber&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-6 (new)]]&#039;&#039;&#039;, Elih Velazquez&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Influenza A M2 transmembrane domain]]&#039;&#039;&#039;, Samantha Nicholls&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Dengue Virus Protease]]&#039;&#039;&#039;, Muslum Yildiz&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Hebert Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular_Playground/Hsp70-Hsp90]]&#039;&#039;&#039;,  Jill Graham&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular_Playground/ERDj5]]&#039;&#039;&#039;,  Lydia Lamriben&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Saposin C]]&#039;&#039;&#039;, Abla Tannous&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular_Playground/ERMan1]]&#039;&#039;&#039;,  Johan Sunryd&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.biochem.umass.edu/aheuck/aph.html Heuck Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular_Playground/Pcr H]]&#039;&#039;&#039;,  Fabian Romano, Carolina Morell-Pérez&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/mholden/ Holden Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Protective Antigen]]&#039;&#039;&#039;,  Jing Huang&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/people/kaltashovlab/ Kaltashov Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[http://proteopedia.org/wiki/index.php/Chengfeng_Ren Molecular Playground/Inteferon]&#039;&#039;&#039;, Chengfeng Ren&lt;br /&gt;
: &#039;&#039;&#039; [[Molecular Playground/Transferrin]]&#039;&#039;&#039;, Khaja Muneeruddin, Jake Pawlowski&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Velaglucerase]]&#039;&#039;&#039;, Adriana Kita&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Antithrombin-Heparin]]&#039;&#039;&#039;, Yunlong Zhao&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Knapp lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/FIH]]&#039;&#039;&#039;, Vanessa Chaplin, Cornelius Taabazuing, Breanne Holmes, John Hangasky&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Prolyl Hydroxylase Domain (PHD) Enzyme]]&#039;&#039;&#039;, Cristina Martin, Serap Pektas &#039;&#039;&#039;Best CBI Molecule Proteopedia Page 2010&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/mmaroney/ Maroney Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Nickel Superoxide Dismutase]]&#039;&#039;&#039;, Carolyn Carr&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CsoR and RcnR]]&#039;&#039;&#039;, Heidi Hu, Carolyn Carr&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/HypA]]&#039;&#039;&#039;, Heidi Hu&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/~cmartin/ Martin Lab]&lt;br /&gt;
&lt;br /&gt;
: **&#039;&#039;&#039;[[Molecular Playground/T7 RNAP Conformations]]&#039;&#039;&#039;, Luis E. Ramirez-Tapia &#039;&#039;&#039;Best CBI Molecule 2011&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/T7 RNA Polymerase (7 mer int)]]&#039;&#039;&#039;, Ankit Vahia&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Human mtRNA pol]]&#039;&#039;&#039;, Ketan Mathavan &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.peytonlab.org/ Peyton Lab]&lt;br /&gt;
: &amp;quot;&#039;[[Molecular Playground/IntegrinBeta1]]&#039;&amp;quot;, Lauren Jansen, Lauren Barney, Elizabeth Brooks, Alyssa Schwartz&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/MMP14]]&#039;&#039;&#039;, Lauren Jansen&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/C-Raf]]&#039;&#039;&#039;, Thuy Nguyen&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/FAK]]&#039;&#039;&#039;, Dannielle Ryman&lt;br /&gt;
&lt;br /&gt;
[http://roberts.openwetware.org/ Roberts Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Taxol]]&#039;&#039;&#039;,  Rohan Patil, Sarah Wilson&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Insulin]]&#039;&#039;&#039;, Whitney Stoppel&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.umass.edu/rotellogroup/ Rotello Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Reverse transcriptase|Molecular Playground/Reverse Transcriptase]]&#039;&#039;&#039;, Daniel Moyano-Marino&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Pancreatic Lipase]]&#039;&#039;&#039;,  Rui Tang&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular playground/Chymotrypsin]]&#039;&#039;&#039;,  Brad&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Targeting Peptide]]&#039;&#039;&#039;, David Solfiell&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://http://www.umass.edu/schiffman/  Schiffman Lab]&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Streptavidin]]&#039;&#039;&#039;, Katrina Rieger&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.biochem.umass.edu/faculty/danny-j-schnell Schnell Lab]&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Tic40]]&#039;&#039;&#039;, Mine Canakci&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Tew Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/HIV Tat]]&#039;&#039;&#039;, Brittany deRonde&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Thayumanavan Lab&lt;br /&gt;
: &#039;&#039;&#039;[[Interleukin-1 beta]]&#039;&#039;&#039;, Huan He&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Lysozyme ]]&#039;&#039;&#039;, Daniella Gonzalez&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Beta-galactosidase]]&#039;&#039;&#039;, Judy Ventura&lt;br /&gt;
: &#039;&#039;&#039;[[User:Krishna Reddy Ragupathi|Molecular Playground/Carbonic Anhydrase]]&#039;&#039;&#039;, Krishna Reddy Raghupathi&lt;br /&gt;
: &#039;&#039;&#039;[[User:Rami Rajasekhar Reddy|Molecular Playground/Avidin]]&#039;&#039;&#039;, Rami Rajasekar Reddy&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Biotin binding avidin]]&#039;&#039;&#039;, Diego Amado &lt;br /&gt;
: &#039;&#039;&#039;[[User:Jiaming Zhuang|Molecular Playground/MMP12]]&#039;&#039;&#039;, Jiaming Zhuang&lt;br /&gt;
: &#039;&#039;&#039; [[User:Jing Guo|Molecular Playground/Gluconase]]&#039;&#039;&#039;, Jing Guo&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Glutathione Reductase]]&#039;&#039;&#039;, Reuben Chacko&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Thayumanavan &amp;amp; Vachet Labs&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Trypsin]]&#039;&#039;&#039;, Gladys Murage&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/thompson/index.html Thompson Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Bacterial Chemotaxis Complex]]&#039;&#039;&#039;, Elizabeth R. Haglin, Maryam Kashefi&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CheA]]&#039;&#039;&#039;, Elizabeth R. Haglin&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Bacterial Chemotaxis Receptors]]&#039;&#039;&#039;, Lynmarie K. Thompson, Shiela M. Jones&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Cytoplasmic domain of chemoreceptor of Thermotoga maritima]]&#039;&#039;&#039;,  Xuni Li&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/~vachet/index.html Vachet Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;[[Molecular Playground/Human Serum Albumin]]&#039;&#039;&#039;, Mahalia Serrano&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular playground/beta 2 microglobulin]]&#039;&#039;&#039;,  Nick Borotto &#039;&#039;&#039;Best CBI Molecule Jmol scenes 2010&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Myoglobin]]&#039;&#039;&#039;,  Yuping Zhou &lt;br /&gt;
:&#039;&#039;&#039;[[Molecular Playground/ Copper-Zinc Superoxide Dismutase]]&#039;&#039;&#039;, Shaynah Browne&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Ubiquitin salt bridge discussion]]&#039;&#039;&#039;, Zhe Zhang&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Other Molecules of interest&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/PcrA Helicase]]&#039;&#039;&#039;, Luis E Ramirez-Tapia, [http://www.chem.umass.edu/~cmartin/ Martin Lab]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Other Laboratories&lt;br /&gt;
&lt;br /&gt;
:&#039;&#039;&#039;[[Molecular Playground/4&#039;-PHOSPHOPANTETHEINYL TRANSFERASE (Sfp)]]&#039;&#039;&#039;, Jon Amoroso, Gitanjeli Prasad, Lawrence Sheringham Borketey, Schnarr lab&lt;br /&gt;
: &#039;&#039;&#039;[[6-deoxyerythronolide_B_synthase_(DEBS)|Molecular Playground/6-Deoxyerythronolide B Synthase]]&#039;&#039;&#039;, Tsung-Yi Lin, Jon Amoroso, Lawrence Sheringham Borketey, Schnarr lab&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/ACP apo]]&#039;&#039;&#039;, Gitanjeli Prasad,  Schnarr lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/cytoplasmic domain of a serine chemotaxis receptor]]&#039;&#039;&#039;,  Meili Yang, Weis lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Alginate-Fall2011]]&#039;&#039;&#039;, Joe White, David Griffi, Bhatia Lab&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Poly(ethylene glycol)]]&#039;&#039;&#039;, Erika M. Saffer, Bhatia Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/YKL-40]]&#039;&#039;&#039;, Ralph A. Francescone III, [http://www.bio.umass.edu/mcb/faculty/Shao.html Shao Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/BLG|Molecular Playground/β-lactoglobulin]]&#039;&#039;&#039;, Daniel Seeman, Dubin Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/ADAM13]]&#039;&#039;&#039;, Genevieve Abbruzzese, Alfandari Lab&lt;br /&gt;
&lt;br /&gt;
==Instructions==&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;The goal is for students to work collaboratively to create one excellent CBI Molecule for each CBI research group, to be featured on the CBI website.&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Fall 2014: Complete steps 1-3 before the CBI Molecule Workshop on 11/19; bring your computer to the CBI Molecule Workshop in ISB 321. You will be able to start work on your CBI Molecule at the workshop. You should plan to stay and finish your molecule after the workshop (or as soon as possible) while the instructions and ideas are fresh in your mind.&lt;br /&gt;
&lt;br /&gt;
A successful CBI Molecule is an interesting, nontechnical description of a molecule related to your group&#039;s research. It should tell an interesting story with few words and many green scenes. Green scenes should be clear and attractive illustrations that tell your story. It&#039;s great if you can end with a brief statement about how it relates to your group&#039;s research goals.&lt;br /&gt;
&lt;br /&gt;
1. If you don&#039;t already have one, request a Proteopedia account and log in. &lt;br /&gt;
&lt;br /&gt;
2. Read through the rest of the instructions, do the tutorials below, and look at any existing CBI Molecules from your research group. Talk with other CBI students in your research group and decide how you will collaborate to make an improved CBI Molecule related to your group&#039;s research. Develop ideas for the scenes that each of you will make.&lt;br /&gt;
&lt;br /&gt;
3. Get started working in Proteopedia. Make yourself a sandbox page: Enter &amp;quot;User:Your Name/Sandbox 1&amp;quot; (omit quotes) in the search box, then follow instructions to edit this page. Practice entering text, inserting a structure window with scrolling text (green 4-square button on the right), and creating a green scene. Explore the HELP links below to learn how to make a green scene. You can look at other Proteopedia pages in edit mode to see how different effects (like colored text) are achieved (but this won&#039;t show you how the scene effects are made). &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Complete the above steps before the CBI Molecule Workshop.&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
4. When editing an existing CBI Molecule, leave the original intact and make a copy that you will edit so that it retains the full author list of all authors that contributed. You are encouraged to collaborate on the CBI Molecules, but everyone will need to log in as themself and create a green scene to get credit for their work and to appear as authors on the final list. If you are the sole student from your group enrolled in Chalk Talk and have not previously made a CBI Molecule, try to convince another group member who has previously made a CBI Molecule (see  list above) to join us for the workshop so that you can work together.&lt;br /&gt;
&lt;br /&gt;
5. Your final pages should be called &amp;quot;Molecular Playground/your molecule&amp;quot; and should have links on this CBI Molecule page -- put the new ones first on the list from your research group. Label them &amp;quot;in progress&amp;quot; until you are finished, and then &amp;quot;new 2014&amp;quot; or &amp;quot;revised 2014&amp;quot;. Minimize text; tell your story with green scenes!&lt;br /&gt;
&lt;br /&gt;
6. When your CBI Molecule is complete, send Lynmarie an email to nominate a cool scene/clever caption you would like to feature at the Molecular Playground (include a link to your CBI Molecule, name of the green scene, and caption).&lt;br /&gt;
&lt;br /&gt;
==Links to HELP pages==&lt;br /&gt;
Overview at [[Help:Contents ]]&lt;br /&gt;
&lt;br /&gt;
See also [[Help:Getting_Started_in_Proteopedia]] &lt;br /&gt;
&lt;br /&gt;
Videos showing how to use Proteopedia:&lt;br /&gt;
[[Proteopedia:Video_Guide]]&lt;br /&gt;
(Sometimes slow -- if you pause the video and wait awhile it will download and then you can play it without interruptions)&lt;br /&gt;
&lt;br /&gt;
[[Proteopedia:DIY:Scenes|Proteopedia Scenes: Do It Yourself]]&lt;br /&gt;
gives succinct step by step instructions on how to create a molecular scene.&lt;br /&gt;
&lt;br /&gt;
A powerpoint-like set of slides that walks a user through the process of creating a new page and a new molecular scene/green link.&lt;br /&gt;
[http://www.proteopedia.org/wiki/images/1/1b/2009_07_13_Proteopedia_Workshop.pdf Proteopedia Workshop Slides]&lt;br /&gt;
&lt;br /&gt;
[[Proteopedia:Guidelines for Ethical Writing]].&lt;br /&gt;
Please pay attention to the section about images. There are links to examples of images re-used with explicit permission.&lt;br /&gt;
&lt;br /&gt;
For other help resources, click on [[Help:Contents|Help]] in the &#039;&#039;navigation&#039;&#039; box at the upper left of every page in Proteopedia.&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=CBI_Molecules&amp;diff=2065505</id>
		<title>CBI Molecules</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=CBI_Molecules&amp;diff=2065505"/>
		<updated>2014-11-19T17:29:49Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;These are molecules under study by members of the [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program].&lt;br /&gt;
Many of the  molecules we study are featured at the [http://www.molecularplayground.org/ Molecular Playground] (see also [[Molecular Playground|Molecular Playground in Proteopedia]]). Follow the links below to read nontechnical descriptions, in Proteopedia, of these molecules.&lt;br /&gt;
&lt;br /&gt;
UMass CBI Members, add your molecules to the list (which is alphabetical by CBI research mentor); follow the instructions below the list.&lt;br /&gt;
&lt;br /&gt;
Fall 2014: CBI Molecules are due 12/3/14 and should be added at the TOP of the list from your lab. Label it as &amp;quot;in progress&amp;quot; until you are finished, and then as &amp;quot;New 2014&amp;quot; or &amp;quot;Revised 2014&amp;quot;. For those editing an existing CBI Molecule, start by making a copy of that entry (leaving the original intact) so that it retains the full author list of all authors that contributed (or include credits and a link to the original page and authors if it does not).&lt;br /&gt;
Follow the instructions at the bottom of this page.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Molecules==&lt;br /&gt;
&#039;&#039;&#039;** Designates CBI Molecules Featured on [http://www.umass.edu/cbi/ CBI website]&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
[http://chamberslab.com/wp/ Chambers Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Glutamate Receptor]]&#039;&#039;&#039;,  Amanda Hussey, Steve McCarron, Rosie Combs-Bachmann, Mariel Feliciano&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/~chenlab/index.HTML Chen Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/ClyA]]&#039;&#039;&#039;, Bib Yang&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/OmpG]]&#039;&#039;&#039;, Christina Chisholm&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://openwetware.org/wiki/Chien Chien Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Homo-dimeric RcdA]]&#039;&#039;&#039;, Kamal K. Joshi &lt;br /&gt;
: **&#039;&#039;&#039;[[Molecular Playground/Hexameric ClpX]]&#039;&#039;&#039;, Joanne Lau &#039;&#039;&#039;Best CBI Molecule 2011&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/DNA replication initiator DnaA]]&#039;&#039;&#039;, Jing Liu&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Farkas Lab&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Forbes Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CheR]]&#039;&#039;&#039;,  Miaomin Zhang&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/RBP]]&#039;&#039;&#039;,  Jan Panteli&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/TRAIL]]&#039;&#039;&#039;,  Charley Swofford&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.biochem.umass.edu/garman/index.html Garman Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Human Protective Protein Cathepsin A]]&#039;&#039;&#039;, Yadilette Rivera-Colon&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Human PPCA]]&#039;&#039;&#039;, Nilima Kolli&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/gieraschlab/ Gierasch Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[CRABP I ( Cellular Retinoic Acid Binding Protein )|Molecular Playground/CRABP I]]&#039;&#039;&#039;, Kristine Faye Pobre, Mylene Ferrolino,Mangai Periasamy  &#039;&#039;&#039;Best Overall CBI Molecule 2010&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CRABP I (Cellular Retinoic Acid Binding Protein)]]&#039;&#039;&#039;, Gustavo Elberto Epalza Sanchez&lt;br /&gt;
: **&#039;&#039;&#039;[[Molecular_Playground/DHFR]]&#039;&#039;&#039;, Karan Hingorani &#039;&#039;&#039;Best CBI Molecule 2012&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/jhardy/ Hardy Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Executioner Caspase-7]]&#039;&#039;&#039;, Derek MacPherson, Maureen E. Hill&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-3 Regulatory Mechanisms]]&#039;&#039;&#039;, Scott Eron, Bay Serrano, Yunlong Zhao&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-6 and neurodegeneration]]&#039;&#039;&#039;, Kevin Buadlart Dagbay&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-7 Dynamics]]&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-9 Regulation]]&#039;&#039;&#039;, Kristen Huber&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-6 (new)]]&#039;&#039;&#039;, Elih Velazquez&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Influenza A M2 transmembrane domain]]&#039;&#039;&#039;, Samantha Nicholls&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Dengue Virus Protease]]&#039;&#039;&#039;, Muslum Yildiz&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Hebert Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular_Playground/Hsp70-Hsp90]]&#039;&#039;&#039;,  Jill Graham&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular_Playground/ERDj5]]&#039;&#039;&#039;,  Lydia Lamriben&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Saposin C]]&#039;&#039;&#039;, Abla Tannous&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular_Playground/ERMan1]]&#039;&#039;&#039;,  Johan Sunryd&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.biochem.umass.edu/aheuck/aph.html Heuck Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular_Playground/Pcr H]]&#039;&#039;&#039;,  Fabian Romano, Carolina Morell-Pérez&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/mholden/ Holden Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Protective Antigen]]&#039;&#039;&#039;,  Jing Huang&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/people/kaltashovlab/ Kaltashov Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[http://proteopedia.org/wiki/index.php/Chengfeng_Ren Molecular Playground/Inteferon]&#039;&#039;&#039;, Chengfeng Ren&lt;br /&gt;
: &#039;&#039;&#039; [[Molecular Playground/Transferrin]]&#039;&#039;&#039;, Khaja Muneeruddin, Jake Pawlowski&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Velaglucerase]]&#039;&#039;&#039;, Adriana Kita&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Antithrombin-Heparin]]&#039;&#039;&#039;, Yunlong Zhao&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Knapp lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/FIH]]&#039;&#039;&#039;, Vanessa Chaplin, Cornelius Taabazuing, Breanne Holmes, John Hangasky&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Prolyl Hydroxylase Domain (PHD) Enzyme]]&#039;&#039;&#039;, Cristina Martin, Serap Pektas &#039;&#039;&#039;Best CBI Molecule Proteopedia Page 2010&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/mmaroney/ Maroney Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Nickel Superoxide Dismutase]]&#039;&#039;&#039;, Carolyn Carr&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CsoR and RcnR]]&#039;&#039;&#039;, Heidi Hu, Carolyn Carr&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/HypA]]&#039;&#039;&#039;, Heidi Hu&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/~cmartin/ Martin Lab]&lt;br /&gt;
&lt;br /&gt;
: **&#039;&#039;&#039;[[Molecular Playground/T7 RNAP Conformations]]&#039;&#039;&#039;, Luis E. Ramirez-Tapia &#039;&#039;&#039;Best CBI Molecule 2011&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/T7 RNA Polymerase (7 mer int)]]&#039;&#039;&#039;, Ankit Vahia&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Human mtRNA pol]]&#039;&#039;&#039;, Ketan Mathavan &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.peytonlab.org/ Peyton Lab]&lt;br /&gt;
:&amp;quot;&amp;quot;[[Molecular Playground/IntegrinBeta1]]&amp;quot;&amp;quot;, Lauren Jansen, Lauren Barney, Elizabeth Brooks, Alyssa Schwartz&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/MMP14]]&#039;&#039;&#039;, Lauren Jansen&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/C-Raf]]&#039;&#039;&#039;, Thuy Nguyen&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/FAK]]&#039;&#039;&#039;, Dannielle Ryman&lt;br /&gt;
&lt;br /&gt;
[http://roberts.openwetware.org/ Roberts Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Taxol]]&#039;&#039;&#039;,  Rohan Patil, Sarah Wilson&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Insulin]]&#039;&#039;&#039;, Whitney Stoppel&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.umass.edu/rotellogroup/ Rotello Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Reverse transcriptase|Molecular Playground/Reverse Transcriptase]]&#039;&#039;&#039;, Daniel Moyano-Marino&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Pancreatic Lipase]]&#039;&#039;&#039;,  Rui Tang&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular playground/Chymotrypsin]]&#039;&#039;&#039;,  Brad&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Targeting Peptide]]&#039;&#039;&#039;, David Solfiell&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://http://www.umass.edu/schiffman/  Schiffman Lab]&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Streptavidin]]&#039;&#039;&#039;, Katrina Rieger&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.biochem.umass.edu/faculty/danny-j-schnell Schnell Lab]&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Tic40]]&#039;&#039;&#039;, Mine Canakci&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Tew Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/HIV Tat]]&#039;&#039;&#039;, Brittany deRonde&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Thayumanavan Lab&lt;br /&gt;
: &#039;&#039;&#039;[[Interleukin-1 beta]]&#039;&#039;&#039;, Huan He&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Lysozyme ]]&#039;&#039;&#039;, Daniella Gonzalez&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Beta-galactosidase]]&#039;&#039;&#039;, Judy Ventura&lt;br /&gt;
: &#039;&#039;&#039;[[User:Krishna Reddy Ragupathi|Molecular Playground/Carbonic Anhydrase]]&#039;&#039;&#039;, Krishna Reddy Raghupathi&lt;br /&gt;
: &#039;&#039;&#039;[[User:Rami Rajasekhar Reddy|Molecular Playground/Avidin]]&#039;&#039;&#039;, Rami Rajasekar Reddy&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Biotin binding avidin]]&#039;&#039;&#039;, Diego Amado &lt;br /&gt;
: &#039;&#039;&#039;[[User:Jiaming Zhuang|Molecular Playground/MMP12]]&#039;&#039;&#039;, Jiaming Zhuang&lt;br /&gt;
: &#039;&#039;&#039; [[User:Jing Guo|Molecular Playground/Gluconase]]&#039;&#039;&#039;, Jing Guo&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Glutathione Reductase]]&#039;&#039;&#039;, Reuben Chacko&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Thayumanavan &amp;amp; Vachet Labs&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Trypsin]]&#039;&#039;&#039;, Gladys Murage&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/thompson/index.html Thompson Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Bacterial Chemotaxis Complex]]&#039;&#039;&#039;, Elizabeth R. Haglin, Maryam Kashefi&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CheA]]&#039;&#039;&#039;, Elizabeth R. Haglin&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Bacterial Chemotaxis Receptors]]&#039;&#039;&#039;, Lynmarie K. Thompson, Shiela M. Jones&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Cytoplasmic domain of chemoreceptor of Thermotoga maritima]]&#039;&#039;&#039;,  Xuni Li&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/~vachet/index.html Vachet Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;[[Molecular Playground/Human Serum Albumin]]&#039;&#039;&#039;, Mahalia Serrano&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular playground/beta 2 microglobulin]]&#039;&#039;&#039;,  Nick Borotto &#039;&#039;&#039;Best CBI Molecule Jmol scenes 2010&#039;&#039;&#039;&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Myoglobin]]&#039;&#039;&#039;,  Yuping Zhou &lt;br /&gt;
:&#039;&#039;&#039;[[Molecular Playground/ Copper-Zinc Superoxide Dismutase]]&#039;&#039;&#039;, Shaynah Browne&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Ubiquitin salt bridge discussion]]&#039;&#039;&#039;, Zhe Zhang&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Other Molecules of interest&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/PcrA Helicase]]&#039;&#039;&#039;, Luis E Ramirez-Tapia, [http://www.chem.umass.edu/~cmartin/ Martin Lab]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Other Laboratories&lt;br /&gt;
&lt;br /&gt;
:&#039;&#039;&#039;[[Molecular Playground/4&#039;-PHOSPHOPANTETHEINYL TRANSFERASE (Sfp)]]&#039;&#039;&#039;, Jon Amoroso, Gitanjeli Prasad, Lawrence Sheringham Borketey, Schnarr lab&lt;br /&gt;
: &#039;&#039;&#039;[[6-deoxyerythronolide_B_synthase_(DEBS)|Molecular Playground/6-Deoxyerythronolide B Synthase]]&#039;&#039;&#039;, Tsung-Yi Lin, Jon Amoroso, Lawrence Sheringham Borketey, Schnarr lab&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/ACP apo]]&#039;&#039;&#039;, Gitanjeli Prasad,  Schnarr lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/cytoplasmic domain of a serine chemotaxis receptor]]&#039;&#039;&#039;,  Meili Yang, Weis lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Alginate-Fall2011]]&#039;&#039;&#039;, Joe White, David Griffi, Bhatia Lab&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Poly(ethylene glycol)]]&#039;&#039;&#039;, Erika M. Saffer, Bhatia Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/YKL-40]]&#039;&#039;&#039;, Ralph A. Francescone III, [http://www.bio.umass.edu/mcb/faculty/Shao.html Shao Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/BLG|Molecular Playground/β-lactoglobulin]]&#039;&#039;&#039;, Daniel Seeman, Dubin Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/ADAM13]]&#039;&#039;&#039;, Genevieve Abbruzzese, Alfandari Lab&lt;br /&gt;
&lt;br /&gt;
==Instructions==&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;The goal is for students to work collaboratively to create one excellent CBI Molecule for each CBI research group, to be featured on the CBI website.&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Fall 2014: Complete steps 1-3 before the CBI Molecule Workshop on 11/19; bring your computer to the CBI Molecule Workshop in ISB 321. You will be able to start work on your CBI Molecule at the workshop. You should plan to stay and finish your molecule after the workshop (or as soon as possible) while the instructions and ideas are fresh in your mind.&lt;br /&gt;
&lt;br /&gt;
A successful CBI Molecule is an interesting, nontechnical description of a molecule related to your group&#039;s research. It should tell an interesting story with few words and many green scenes. Green scenes should be clear and attractive illustrations that tell your story. It&#039;s great if you can end with a brief statement about how it relates to your group&#039;s research goals.&lt;br /&gt;
&lt;br /&gt;
1. If you don&#039;t already have one, request a Proteopedia account and log in. &lt;br /&gt;
&lt;br /&gt;
2. Read through the rest of the instructions, do the tutorials below, and look at any existing CBI Molecules from your research group. Talk with other CBI students in your research group and decide how you will collaborate to make an improved CBI Molecule related to your group&#039;s research. Develop ideas for the scenes that each of you will make.&lt;br /&gt;
&lt;br /&gt;
3. Get started working in Proteopedia. Make yourself a sandbox page: Enter &amp;quot;User:Your Name/Sandbox 1&amp;quot; (omit quotes) in the search box, then follow instructions to edit this page. Practice entering text, inserting a structure window with scrolling text (green 4-square button on the right), and creating a green scene. Explore the HELP links below to learn how to make a green scene. You can look at other Proteopedia pages in edit mode to see how different effects (like colored text) are achieved (but this won&#039;t show you how the scene effects are made). &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Complete the above steps before the CBI Molecule Workshop.&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
4. When editing an existing CBI Molecule, leave the original intact and make a copy that you will edit so that it retains the full author list of all authors that contributed. You are encouraged to collaborate on the CBI Molecules, but everyone will need to log in as themself and create a green scene to get credit for their work and to appear as authors on the final list. If you are the sole student from your group enrolled in Chalk Talk and have not previously made a CBI Molecule, try to convince another group member who has previously made a CBI Molecule (see  list above) to join us for the workshop so that you can work together.&lt;br /&gt;
&lt;br /&gt;
5. Your final pages should be called &amp;quot;Molecular Playground/your molecule&amp;quot; and should have links on this CBI Molecule page -- put the new ones first on the list from your research group. Label them &amp;quot;in progress&amp;quot; until you are finished, and then &amp;quot;new 2014&amp;quot; or &amp;quot;revised 2014&amp;quot;. Minimize text; tell your story with green scenes!&lt;br /&gt;
&lt;br /&gt;
6. When your CBI Molecule is complete, send Lynmarie an email to nominate a cool scene/clever caption you would like to feature at the Molecular Playground (include a link to your CBI Molecule, name of the green scene, and caption).&lt;br /&gt;
&lt;br /&gt;
==Links to HELP pages==&lt;br /&gt;
Overview at [[Help:Contents ]]&lt;br /&gt;
&lt;br /&gt;
See also [[Help:Getting_Started_in_Proteopedia]] &lt;br /&gt;
&lt;br /&gt;
Videos showing how to use Proteopedia:&lt;br /&gt;
[[Proteopedia:Video_Guide]]&lt;br /&gt;
(Sometimes slow -- if you pause the video and wait awhile it will download and then you can play it without interruptions)&lt;br /&gt;
&lt;br /&gt;
[[Proteopedia:DIY:Scenes|Proteopedia Scenes: Do It Yourself]]&lt;br /&gt;
gives succinct step by step instructions on how to create a molecular scene.&lt;br /&gt;
&lt;br /&gt;
A powerpoint-like set of slides that walks a user through the process of creating a new page and a new molecular scene/green link.&lt;br /&gt;
[http://www.proteopedia.org/wiki/images/1/1b/2009_07_13_Proteopedia_Workshop.pdf Proteopedia Workshop Slides]&lt;br /&gt;
&lt;br /&gt;
[[Proteopedia:Guidelines for Ethical Writing]].&lt;br /&gt;
Please pay attention to the section about images. There are links to examples of images re-used with explicit permission.&lt;br /&gt;
&lt;br /&gt;
For other help resources, click on [[Help:Contents|Help]] in the &#039;&#039;navigation&#039;&#039; box at the upper left of every page in Proteopedia.&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065492</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065492"/>
		<updated>2014-11-19T17:27:48Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
==Disease==&lt;br /&gt;
&lt;br /&gt;
==Studying Integrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065485</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065485"/>
		<updated>2014-11-19T17:27:27Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
==Studying Intergrin Beta-1&#039;&#039; in vitro&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065471</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065471"/>
		<updated>2014-11-19T17:26:27Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;br /&gt;
&lt;br /&gt;
==Peyton Lab Research Interests==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065469</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065469"/>
		<updated>2014-11-19T17:25:46Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 binds to ECM proteins and allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
&lt;br /&gt;
==Function==&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065466</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065466"/>
		<updated>2014-11-19T17:23:44Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&#039;&#039;&#039; Integrin Beta 1 allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065465</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065465"/>
		<updated>2014-11-19T17:23:19Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Banner:&amp;quot;&amp;quot; Integrin Beta 1 allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065464</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065464"/>
		<updated>2014-11-19T17:22:54Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&#039;Integrin Beta 1 allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&amp;quot;&#039;&#039;&#039;&#039;&#039;&#039;&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065463</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065463"/>
		<updated>2014-11-19T17:22:17Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
&lt;br /&gt;
Integrin Beta 1 allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&amp;quot;&#039;&#039;&#039;&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065462</id>
		<title>Molecular Playground/IntegrinBeta1</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/IntegrinBeta1&amp;diff=2065462"/>
		<updated>2014-11-19T17:19:36Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: New page: One of the CBI Molecules being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at th...&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
Integrin Beta 1 allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&amp;quot;&#039;&#039;&#039;&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/MMP14&amp;diff=1873395</id>
		<title>Molecular Playground/MMP14</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/MMP14&amp;diff=1873395"/>
		<updated>2013-12-06T20:51:01Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
MMP-14 allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&amp;quot;&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
Membrane Type 1 Matrix Metalloproteinase (MT1-MMP) is 1 of ~24 members of the MMP family of endopeptidases.  MMPs are zinc dependent proteinases that are capable of degrading virtually any extracellular matrix component [1].  Inherently, this enables MMPs to be a key player in regulation of cell behavior.  There are 8 structure classes for MMPs and of these classes,  5 are secreted molecules and 3 are membrane-type [2]. MT1-MMP or also known as MMP-14 is covalently linked to the cell membrane. &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3C7X&#039; size=&#039;400&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;PBD file obtained from http://pdb.org/pdb/explore/explore.do?structureId=3C7X &#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
More information on MMPs can be found on proteopedia at [[MMP]].&lt;br /&gt;
&lt;br /&gt;
==Inhibition==&lt;br /&gt;
&lt;br /&gt;
Tissue inhibitors of metalloproteinases (TIMPs)  are small molecules that can regulate the activity of MMPs. &amp;lt;scene name=&#039;56/567281/2/1&#039;&amp;gt;TIMP-2&amp;lt;/scene&amp;gt; is capable of binding the &amp;lt;scene name=&#039;56/567281/2/5&#039;&amp;gt;catalytic domain&amp;lt;/scene&amp;gt; of MMP-14, creating a new cell surface &amp;lt;scene name=&#039;56/567281/2/4&#039;&amp;gt;molecule&amp;lt;/scene&amp;gt; involved in the activation of MMP-2 [3].&lt;br /&gt;
&lt;br /&gt;
==Extracellular Matrix Components==&lt;br /&gt;
MMP-14 degrades the following substrates in the extracellular matrix [2]:&lt;br /&gt;
:Aggrecan&lt;br /&gt;
:Collagen I&lt;br /&gt;
:Collagen II&lt;br /&gt;
:Collagen III&lt;br /&gt;
:Entactin/Nidogen&lt;br /&gt;
:Fibrillin&lt;br /&gt;
:Fibronectin&lt;br /&gt;
:Gelatin I&lt;br /&gt;
:Laminin&lt;br /&gt;
:Vitronectin&lt;br /&gt;
:α2-M&lt;br /&gt;
:α1-PI&lt;br /&gt;
:Factor XII&lt;br /&gt;
:Fibrin&lt;br /&gt;
:Fibrinogen&lt;br /&gt;
:ProMMP2&lt;br /&gt;
:ProTNFα&lt;br /&gt;
&lt;br /&gt;
==My Research Interest==&lt;br /&gt;
&lt;br /&gt;
In the [http://www.peytonlab.org/ Peyton Lab] I work to combine materials science with stem cell and cancer biology to design &#039;&#039;in vitro&#039;&#039; model biomaterial systems to understand cell motility. My project aims to design 3D biomaterial tissue mimics using poly(ethylene glycol). I incorporate degradable MMP crosslinkers into these biomaterials to allow cells the opportunity to move throughout the matrix and remodel their surrounding microenvironment.&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&lt;br /&gt;
[1]  L. Coussens, et al., Matrix Metalloproteinase Inhibitors and Cancer: Trials and Tribulations, Science, 2002. 295: p. 2387-92&lt;br /&gt;
&lt;br /&gt;
[2] M. Sternlicht, et al., How Matrix Metalloproteinases Regulate Cell Behavior,  Annu Rev Cell Dev Biol,  2001. 17: p. 463–516.&lt;br /&gt;
&lt;br /&gt;
[3] Egeblad, et. al., New Functions for the Matrix Metalloproteinases in Cancer Progression, Nat. Rev. Can., 2002, 2: 162-74&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=CBI_Molecules&amp;diff=1873394</id>
		<title>CBI Molecules</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=CBI_Molecules&amp;diff=1873394"/>
		<updated>2013-12-06T20:50:32Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;These are molecules under study by members of the [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program].&lt;br /&gt;
Many of the  molecules we study are featured at the [http://www.molecularplayground.org/ Molecular Playground] (see also [[Molecular Playground|Molecular Playground in Proteopedia]]). Follow the links below to read nontechnical descriptions, in Proteopedia, of these molecules.&lt;br /&gt;
&lt;br /&gt;
UMass CBI Members, add your molecules to the list (which is alphabetical by CBI research mentor); follow the instructions below the list.&lt;br /&gt;
&lt;br /&gt;
Fall 2013: CBI Molecules are due 12/4/13 and should be added at the TOP of the list from your lab. Label it as &amp;quot;in progress&amp;quot; until you are finished, and then as &amp;quot;New 2013&amp;quot; or &amp;quot;Revised 2013&amp;quot;. For those editing an existing CBI Molecule, start from that entry so that it retains the full author list of all authors that contributed (or include credits to the original page and authors if it does not).&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==Molecules==&lt;br /&gt;
&#039;&#039;&#039;** Designates CBI Molecules Featured on [http://http://www.umass.edu/cbi/ CBI website]&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Bhatia Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Alginate-Fall2011]]&#039;&#039;&#039;, Joe White, David Griffin&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Alginate-Fall2010]]&#039;&#039;&#039;, Joe White, David Griffin&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Poly(ethylene glycol)]]&#039;&#039;&#039;, Erika M. Saffer&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://chamberslab.com/wp/ Chambers Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Glutamate Receptor]]&#039;&#039;&#039;,  Amanda Hussey, Steve McCarron, Rosie Combs-Bachmann, Mariel Feliciano&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/~chenlab/index.HTML Chen Lab]&lt;br /&gt;
&lt;br /&gt;
: New Fall 2012!! &#039;&#039;&#039;[[Molecular Playground/OmpG]]&#039;&#039;&#039;, Christina Chisholm&lt;br /&gt;
: New Fall 2013!! &#039;&#039;&#039;[[Molecular Playground/ClyA]]&#039;&#039;&#039;, Bib Yang&lt;br /&gt;
&lt;br /&gt;
[http://openwetware.org/wiki/Chien Chien Lab]&lt;br /&gt;
&lt;br /&gt;
New Fall 2013! : **&#039;&#039;&#039;[[Molecular Playground/Homo-dimeric RcdA]]&#039;&#039;&#039;, Kamal K. Joshi &lt;br /&gt;
&lt;br /&gt;
: **&#039;&#039;&#039;[[Molecular Playground/Hexameric ClpX]]&#039;&#039;&#039;, Joanne Lau &lt;br /&gt;
:: Best CBI Molecule 2011&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/DNA replication initiator DnaA]]&#039;&#039;&#039;, Jing Liu&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Forbes Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CheR]]&#039;&#039;&#039;,  Miaomin Zhang&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/RBP]]&#039;&#039;&#039;,  Jan Panteli&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/TRAIL]]&#039;&#039;&#039;,  Charley Swofford&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.biochem.umass.edu/garman/index.html Garman Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Human Protective Protein Cathepsin A]]&#039;&#039;&#039;, Yadilette Rivera-Colon&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Human PPCA]]&#039;&#039;&#039;, Nilima Kolli&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/gieraschlab/ Gierasch Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[CRABP I ( Cellular Retinoic Acid Binding Protein )|Molecular Playground/CRABP I]]&#039;&#039;&#039;, Kristine Faye Pobre, Mylene Ferrolino,Mangai Periasamy&lt;br /&gt;
:: Best Overall CBI Molecule 2010&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/CRABP I (Cellular Retinoic Acid Binding Protein)]]&#039;&#039;&#039;, Gustavo Elberto Epalza Sanchez&lt;br /&gt;
(compare this to the previous version above to see what&#039;s new)&lt;br /&gt;
&lt;br /&gt;
: **&#039;&#039;&#039;[[Molecular_Playground/DHFR]]&#039;&#039;&#039;, Karan Hingorani &lt;br /&gt;
:: Best CBI Molecule 2012&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/jhardy/ Hardy Lab]&lt;br /&gt;
&lt;br /&gt;
: New Fall 2013!! &#039;&#039;&#039;[[Molecular Playground/Executioner Caspase-7]]&#039;&#039;&#039;, Derek MacPherson, Maureen E. Hill&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/[[Caspase-3 Regulatory Mechanisms]]&#039;&#039;&#039;, Scott Eron, Bay Serrano, Yunlong Zhao&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039; [[Molecular Playground/Caspase-6 and neurodegeneration]]&#039;&#039;&#039;, Kevin Buadlart Dagbay&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-7 Dynamics]]&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-9 Regulation]]&#039;&#039;&#039;, Kristen Huber&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Caspase-6 (new)]]&#039;&#039;&#039;, Elih Velazquez&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Influenza A M2 transmembrane domain]]&#039;&#039;&#039;, Samantha Nicholls&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Dengue Virus Protease]]&#039;&#039;&#039;, Muslum Yildiz&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Hebert Lab&lt;br /&gt;
&lt;br /&gt;
: New Fall 2013!! &#039;&#039;&#039;[[Molecular_Playground/Hsp70-Hsp90]]&#039;&#039;&#039;,  Jill Graham&lt;br /&gt;
: New Fall 2012!! &#039;&#039;&#039;[[Molecular_Playground/ERDj5]]&#039;&#039;&#039;,  Lydia Lamriben&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Saposin C]]&#039;&#039;&#039;, Abla Tannous&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular_Playground/ERMan1]]&#039;&#039;&#039;,  Johan Sunryd&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.biochem.umass.edu/aheuck/aph.html Heuck Lab]&lt;br /&gt;
&lt;br /&gt;
: Updated Fall 2012!! &#039;&#039;&#039;[[Molecular_Playground/Pcr H]]&#039;&#039;&#039;,  Fabian Romano, Carolina Morell-Pérez&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/mholden/ Holden Lab]&lt;br /&gt;
&lt;br /&gt;
: New Fall 2012!! &#039;&#039;&#039;[[Molecular Playground/Protective Antigen]]&#039;&#039;&#039;,  Jing Huang&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/people/kaltashovlab/ Kaltashov Lab]&lt;br /&gt;
&lt;br /&gt;
New 2013! &#039;&#039;&#039;[http://proteopedia.org/wiki/index.php/Chengfeng_Ren Molecular Playground/Inteferon]&#039;&#039;&#039;, Chengfeng Ren&lt;br /&gt;
&lt;br /&gt;
: Updated Fall 2012!! &#039;&#039;&#039; [[Molecular Playground/Transferrin]]&#039;&#039;&#039;, Khaja Muneeruddin, Jake Pawlowski&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Velaglucerase]]&#039;&#039;&#039;, Adriana Kita&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Knapp lab&lt;br /&gt;
&lt;br /&gt;
: Updated Fall 2013!! &#039;&#039;&#039;[[Molecular Playground/FIH]]&#039;&#039;&#039;, Vanessa Chaplin, Cornelius Taabazuing, Breanne Holmes, John Hangasky&lt;br /&gt;
 &lt;br /&gt;
: Updated Fall 2012!! &#039;&#039;&#039;[[Molecular Playground/Prolyl Hydroxylase Domain (PHD) Enzyme]]&#039;&#039;&#039;, Cristina Martin, Serap Pektas&lt;br /&gt;
:: Best CBI Molecule Proteopedia Page 2010&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/mmaroney/ Maroney Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Nickel Superoxide Dismutase]]&#039;&#039;&#039;, Carolyn Carr&lt;br /&gt;
: Updated Fall 2013!!  &#039;&#039;&#039;[[Molecular Playground/CsoR and RcnR]]&#039;&#039;&#039;, Heidi Hu, Carolyn Carr&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/HypA]]&#039;&#039;&#039;, Heidi Hu&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/~cmartin/ Martin Lab]&lt;br /&gt;
&lt;br /&gt;
: **&#039;&#039;&#039;[[Molecular Playground/T7 RNAP Conformations]]&#039;&#039;&#039;, Luis E. Ramirez-Tapia &lt;br /&gt;
:: Best CBI Molecule 2011&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/T7 RNA Polymerase (7 mer int)]]&#039;&#039;&#039;, Ankit Vahia&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Human mtRNA pol]]&#039;&#039;&#039;, Ketan Mathavan &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.peytonlab.org/ Peyton Lab]&lt;br /&gt;
: New Fall 2013! &#039;&#039;&#039;[[Molecular Playground/MMP14]]&#039;&#039;&#039;, Lauren Jansen&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/C-Raf]]&#039;&#039;&#039;, Thuy Nguyen&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/FAK]]&#039;&#039;&#039;, Dannielle Ryman&lt;br /&gt;
&lt;br /&gt;
[http://roberts.openwetware.org/ Roberts Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Taxol]]&#039;&#039;&#039;,  Rohan Patil, Sarah Wilson&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Insulin]]&#039;&#039;&#039;, Whitney Stoppel&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.umass.edu/rotellogroup/ Rotello Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Reverse transcriptase|Molecular Playground/Reverse Transcriptase]]&#039;&#039;&#039;, Daniel Moyano-Marino&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Pancreatic Lipase]]&#039;&#039;&#039;,  Rui Tang&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular playground/Chymotrypsin]]&#039;&#039;&#039;,  Brad&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Targeting Peptide]]&#039;&#039;&#039;, David Solfiell&lt;br /&gt;
&lt;br /&gt;
[http://http://www.umass.edu/schiffman/  Schiffman Lab]&lt;br /&gt;
:New Fall 2013! &#039;&#039;&#039;[[Molecular Playground/Streptavidin]]&#039;&#039;&#039;, Katrina Rieger&lt;br /&gt;
&lt;br /&gt;
[https://elements.chem.umass.edu/schnarrlab/ Schnarr Lab] &lt;br /&gt;
&lt;br /&gt;
: New Fall 2012!! &#039;&#039;&#039;[[Molecular Playground/4&#039;-PHOSPHOPANTETHEINYL TRANSFERASE (Sfp)]]&#039;&#039;&#039;, Jon Amoroso, Gitanjeli Prasad, Lawrence Sheringham Borketey &lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[6-deoxyerythronolide_B_synthase_(DEBS)|Molecular Playground/6-Deoxyerythronolide B Synthase]]&#039;&#039;&#039;, Tsung-Yi Lin, Jon Amoroso, Lawrence Sheringham Borketey&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/ACP apo]]&#039;&#039;&#039;, Gitanjeli Prasad&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.biochem.umass.edu/faculty/danny-j-schnell Schnell Lab]&lt;br /&gt;
: New Fall 2012!! &#039;&#039;&#039;[[Molecular Playground/Tic40]]&#039;&#039;&#039;, Mine Canakci&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Tew Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/HIV Tat]]&#039;&#039;&#039;, Brittany deRonde&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Thayumanavan Lab&lt;br /&gt;
: New Fall 2013!! &#039;&#039;&#039;[[Interleukin-1 beta]]&#039;&#039;&#039;, Huan He&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Lysozyme ]]&#039;&#039;&#039;, Daniella Gonzalez&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Beta-galactosidase]]&#039;&#039;&#039;, Judy Ventura&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[User:Krishna Reddy Ragupathi|Molecular Playground/Carbonic Anhydrase]]&#039;&#039;&#039;, Krishna Reddy Raghupathi&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[User:Rami Rajasekhar Reddy|Molecular Playground/Avidin]]&#039;&#039;&#039;, Rami Rajasekar Reddy&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Biotin binding avidin]]&#039;&#039;&#039;, Diego Amado &lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[User:Jiaming Zhuang|Molecular Playground/MMP12]]&#039;&#039;&#039;, Jiaming Zhuang&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039; [[User:Jing Guo|Molecular Playground/Gluconase]]&#039;&#039;&#039;, Jing Guo&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Glutathione Reductase]]&#039;&#039;&#039;, Reuben Chacko&lt;br /&gt;
&lt;br /&gt;
Thayumanavan &amp;amp; Vachet Labs&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Trypsin]]&#039;&#039;&#039;, Gladys Murage&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://people.chem.umass.edu/thompson/index.html Thompson] &amp;amp; [http://www.chem.umass.edu/~rmweis/weislab/ Weis] Labs&lt;br /&gt;
&lt;br /&gt;
: New Fall 2012!! &#039;&#039;&#039;[[Molecular Playground/CheA]]&#039;&#039;&#039;, Elizabeth R. Haglin&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Bacterial Chemotaxis Receptors]]&#039;&#039;&#039;, Lynmarie K. Thompson, Shiela M. Jones&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/cytoplasmic domain of a serine chemotaxis receptor]]&#039;&#039;&#039;,  Meili Yang&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Cytoplasmic domain of chemoreceptor of Thermotoga maritima]]&#039;&#039;&#039;,  Xuni Li&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[http://www.chem.umass.edu/~vachet/index.html Vachet Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular playground/beta 2 microglobulin]]&#039;&#039;&#039;,  Nick Borotto&lt;br /&gt;
:: Best CBI Molecule Jmol scenes 2010&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/Myoglobin]]&#039;&#039;&#039;,  Yuping Zhou &lt;br /&gt;
&lt;br /&gt;
:&#039;&#039;&#039;[[Molecular Playground/ Copper-Zinc Superoxide Dismutase]]&#039;&#039;&#039;, Shaynah Browne&lt;br /&gt;
&lt;br /&gt;
: New Fall 2012!! &#039;&#039;&#039;[[Molecular Playground/Ubiquitin salt bridge discussion]]&#039;&#039;&#039;, Zhe Zhang&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Other Molecules of interest&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/PcrA Helicase]]&#039;&#039;&#039;, Luis E Ramirez-Tapia, [http://www.chem.umass.edu/~cmartin/ Martin Lab]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Other Laboratories&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/YKL-40]]&#039;&#039;&#039;, Ralph A. Francescone III, [http://www.bio.umass.edu/mcb/faculty/Shao.html Shao Lab]&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/BLG|Molecular Playground/β-lactoglobulin]]&#039;&#039;&#039;, Daniel Seeman, Dubin Lab&lt;br /&gt;
&lt;br /&gt;
: &#039;&#039;&#039;[[Molecular Playground/ADAM13]]&#039;&#039;&#039;, Genevieve Abbruzzese, Alfandari Lab&lt;br /&gt;
&lt;br /&gt;
==Instructions==&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;The goal is for students to work collaboratively to create one excellent CBI Molecule for each CBI research group, to be featured on the CBI website.&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Fall 2013: Complete steps 1-2 by 10/18, and bring your computer to the CBI Molecule Workshop on Wed 10/23 in ISB 321. &lt;br /&gt;
&lt;br /&gt;
A successful CBI Molecule will be an interesting, nontechnical description of a molecule related to your group&#039;s research. It should not be super long, but instead have multiple green scenes. Green scenes should clearly show an interesting feature and should be attractive. Use the green scenes to help you make interesting points about the molecule (do not try to describe every feature of the molecule). It&#039;s great if you can end with a brief statement about how it relates to your group&#039;s research goals.&lt;br /&gt;
&lt;br /&gt;
1. If you don&#039;t already have one, request a Proteopedia account and log in. &lt;br /&gt;
&lt;br /&gt;
2. Read through the rest of the instructions and look at any existing CBI Molecules from your research group. Talk with other Chalk Talk students in your research group and think about how you can make a new or improved CBI Molecule related to your group&#039;s research. Develop ideas for the scenes you wish to show. You will work learn how to make scenes during the workshop. &lt;br /&gt;
&lt;br /&gt;
3. Get started working in Proteopedia by using the links at [[Help:Contents]]. Make yourself a sandbox page: Enter &amp;quot;User:Your Name/Sandbox 1&amp;quot; (omit quotes) in the search box, then follow instructions to edit this page. Practice entering text, inserting a structure window with scrolling text (green 4-square button on the right), and creating a green scene. You can look at other Proteopedia pages in edit mode to see how different effects (like colored text) are achieved (but this won&#039;t show you how the scene effects are made). &lt;br /&gt;
&lt;br /&gt;
4. For those editing an existing CBI Molecule, start from that entry so that it retains the full author list of all authors that contributed. You are encouraged to collaborate on the CBI Molecules, but everyone will need to do some editing of the molecule so that they each appear as authors on the final list. If you are the sole student from your group enrolled in Chalk Talk and have not previously made a CBI Molecule, try to convince another group member who has previously made a CBI Molecule (see  list above) to join us for the workshop so that you can work together.&lt;br /&gt;
&lt;br /&gt;
5. Your final pages should be called &amp;quot;Molecular Playground/your molecule&amp;quot; and should have links on this CBI Molecule page -- put the new ones first on the list from your research group. Label them &amp;quot;in progress&amp;quot; until you are finished, and then &amp;quot;new 2013&amp;quot; or &amp;quot;revised 2013&amp;quot;.&lt;br /&gt;
&lt;br /&gt;
==Links to HELP pages==&lt;br /&gt;
Overview at [[Help:Contents ]]&lt;br /&gt;
&lt;br /&gt;
See also [[Help:Getting_Started_in_Proteopedia]] &lt;br /&gt;
&lt;br /&gt;
Videos showing how to use Proteopedia:&lt;br /&gt;
[[Proteopedia:Video_Guide]]&lt;br /&gt;
(Sometimes slow -- if you pause the video and wait awhile it will download and then you can play it without interruptions)&lt;br /&gt;
&lt;br /&gt;
[[Proteopedia:DIY:Scenes|Proteopedia Scenes: Do It Yourself]]&lt;br /&gt;
gives succinct step by step instructions on how to create a molecular scene.&lt;br /&gt;
&lt;br /&gt;
A powerpoint-like set of slides that walks a user through the process of creating a new page and a new molecular scene/green link.&lt;br /&gt;
[http://www.proteopedia.org/wiki/images/1/1b/2009_07_13_Proteopedia_Workshop.pdf Proteopedia Workshop Slides]&lt;br /&gt;
&lt;br /&gt;
[[Proteopedia:Guidelines for Ethical Writing]].&lt;br /&gt;
Please pay attention to the section about images. There are links to examples of images re-used with explicit permission.&lt;br /&gt;
&lt;br /&gt;
For other help resources, click on [[Help:Contents|Help]] in the &#039;&#039;navigation&#039;&#039; box at the upper left of every page in Proteopedia.&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/MMP14&amp;diff=1861717</id>
		<title>Molecular Playground/MMP14</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/MMP14&amp;diff=1861717"/>
		<updated>2013-11-06T21:55:57Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: /* Inhibition */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
MMp-14 allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&amp;quot;&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
Membrane Type 1 Matrix Metalloproteinase (MT1-MMP) is 1 of ~24 members of the MMP family of endopeptidases.  MMPs are zinc dependent proteinases that are capable of degrading virtually any extracellular matrix component [1].  Inherently, this enables MMPs to be a key player in regulation of cell behavior.  There are 8 structure classes for MMPs and of these classes,  5 are secreted molecules and 3 are membrane-type [2]. MT1-MMP or also known as MMP-14 is covalently linked to the cell membrane. &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3C7X&#039; size=&#039;400&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;PBD file obtained from http://pdb.org/pdb/explore/explore.do?structureId=3C7X &#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
More information on MMPs can be found on proteopedia at [[MMP]].&lt;br /&gt;
&lt;br /&gt;
==Inhibition==&lt;br /&gt;
&lt;br /&gt;
Tissue inhibitors of metalloproteinases (TIMPs)  are small molecules that can regulate the activity of MMPs. &amp;lt;scene name=&#039;56/567281/2/1&#039;&amp;gt;TIMP-2&amp;lt;/scene&amp;gt; is capable of binding the &amp;lt;scene name=&#039;56/567281/2/5&#039;&amp;gt;catalytic domain&amp;lt;/scene&amp;gt; of MMP-14, creating a new cell surface &amp;lt;scene name=&#039;56/567281/2/4&#039;&amp;gt;molecule&amp;lt;/scene&amp;gt; involved in the activation of MMP-2 [3].&lt;br /&gt;
&lt;br /&gt;
==Extracellular Matrix Components==&lt;br /&gt;
MMP-14 degrades the following substrates in the extracellular matrix [2]:&lt;br /&gt;
:Aggrecan&lt;br /&gt;
:Collagen I&lt;br /&gt;
:Collagen II&lt;br /&gt;
:Collagen III&lt;br /&gt;
:Entactin/Nidogen&lt;br /&gt;
:Fibrillin&lt;br /&gt;
:Fibronectin&lt;br /&gt;
:Gelatin I&lt;br /&gt;
:Laminin&lt;br /&gt;
:Vitronectin&lt;br /&gt;
:α2-M&lt;br /&gt;
:α1-PI&lt;br /&gt;
:Factor XII&lt;br /&gt;
:Fibrin&lt;br /&gt;
:Fibrinogen&lt;br /&gt;
:ProMMP2&lt;br /&gt;
:ProTNFα&lt;br /&gt;
&lt;br /&gt;
==My Research Interest==&lt;br /&gt;
&lt;br /&gt;
In the [http://www.peytonlab.org/ Peyton Lab] I work to combine materials science with stem cell and cancer biology to design &#039;&#039;in vitro&#039;&#039; model biomaterial systems to understand cell motility. My project aims to design 3D biomaterial tissue mimics using poly(ethylene glycol). I incorporate degradable MMP crosslinkers into these biomaterials to allow cells the opportunity to move throughout the matrix and remodel their surrounding microenvironment.&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&lt;br /&gt;
[1]  L. Coussens, et al., Matrix Metalloproteinase Inhibitors and Cancer: Trials and Tribulations, Science, 2002. 295: p. 2387-92&lt;br /&gt;
&lt;br /&gt;
[2] M. Sternlicht, et al., How Matrix Metalloproteinases Regulate Cell Behavior,  Annu Rev Cell Dev Biol,  2001. 17: p. 463–516.&lt;br /&gt;
&lt;br /&gt;
[3] Egeblad, et. al., New Functions for the Matrix Metalloproteinases in Cancer Progression, Nat. Rev. Can., 2002, 2: 162-74&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/MMP14&amp;diff=1861716</id>
		<title>Molecular Playground/MMP14</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/MMP14&amp;diff=1861716"/>
		<updated>2013-11-06T21:47:47Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: /* Inhibition */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
MMp-14 allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&amp;quot;&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
Membrane Type 1 Matrix Metalloproteinase (MT1-MMP) is 1 of ~24 members of the MMP family of endopeptidases.  MMPs are zinc dependent proteinases that are capable of degrading virtually any extracellular matrix component [1].  Inherently, this enables MMPs to be a key player in regulation of cell behavior.  There are 8 structure classes for MMPs and of these classes,  5 are secreted molecules and 3 are membrane-type [2]. MT1-MMP or also known as MMP-14 is covalently linked to the cell membrane. &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3C7X&#039; size=&#039;400&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;PBD file obtained from http://pdb.org/pdb/explore/explore.do?structureId=3C7X &#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
More information on MMPs can be found on proteopedia at [[MMP]].&lt;br /&gt;
&lt;br /&gt;
==Inhibition==&lt;br /&gt;
&lt;br /&gt;
Tissue inhibitors of metalloproteinases (TIMPs)  are small molecules that can regulate the activity of MMPs. &amp;lt;scene name=&#039;56/567281/2/1&#039;&amp;gt;TIMP-2&amp;lt;/scene&amp;gt; is capable of binding the &amp;lt;scene name=&#039;56/567281/2/2&#039;&amp;gt;catalytic domain&amp;lt;/scene&amp;gt; of MMP-14, creating a new cell surface &amp;lt;scene name=&#039;56/567281/2/4&#039;&amp;gt;molecule&amp;lt;/scene&amp;gt; involved in the activation of MMP-2 [3].&lt;br /&gt;
&lt;br /&gt;
==Extracellular Matrix Components==&lt;br /&gt;
MMP-14 degrades the following substrates in the extracellular matrix [2]:&lt;br /&gt;
:Aggrecan&lt;br /&gt;
:Collagen I&lt;br /&gt;
:Collagen II&lt;br /&gt;
:Collagen III&lt;br /&gt;
:Entactin/Nidogen&lt;br /&gt;
:Fibrillin&lt;br /&gt;
:Fibronectin&lt;br /&gt;
:Gelatin I&lt;br /&gt;
:Laminin&lt;br /&gt;
:Vitronectin&lt;br /&gt;
:α2-M&lt;br /&gt;
:α1-PI&lt;br /&gt;
:Factor XII&lt;br /&gt;
:Fibrin&lt;br /&gt;
:Fibrinogen&lt;br /&gt;
:ProMMP2&lt;br /&gt;
:ProTNFα&lt;br /&gt;
&lt;br /&gt;
==My Research Interest==&lt;br /&gt;
&lt;br /&gt;
In the [http://www.peytonlab.org/ Peyton Lab] I work to combine materials science with stem cell and cancer biology to design &#039;&#039;in vitro&#039;&#039; model biomaterial systems to understand cell motility. My project aims to design 3D biomaterial tissue mimics using poly(ethylene glycol). I incorporate degradable MMP crosslinkers into these biomaterials to allow cells the opportunity to move throughout the matrix and remodel their surrounding microenvironment.&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&lt;br /&gt;
[1]  L. Coussens, et al., Matrix Metalloproteinase Inhibitors and Cancer: Trials and Tribulations, Science, 2002. 295: p. 2387-92&lt;br /&gt;
&lt;br /&gt;
[2] M. Sternlicht, et al., How Matrix Metalloproteinases Regulate Cell Behavior,  Annu Rev Cell Dev Biol,  2001. 17: p. 463–516.&lt;br /&gt;
&lt;br /&gt;
[3] Egeblad, et. al., New Functions for the Matrix Metalloproteinases in Cancer Progression, Nat. Rev. Can., 2002, 2: 162-74&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/MMP14&amp;diff=1861715</id>
		<title>Molecular Playground/MMP14</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/MMP14&amp;diff=1861715"/>
		<updated>2013-11-06T21:43:18Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: /* Inhibition */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
MMp-14 allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&amp;quot;&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
Membrane Type 1 Matrix Metalloproteinase (MT1-MMP) is 1 of ~24 members of the MMP family of endopeptidases.  MMPs are zinc dependent proteinases that are capable of degrading virtually any extracellular matrix component [1].  Inherently, this enables MMPs to be a key player in regulation of cell behavior.  There are 8 structure classes for MMPs and of these classes,  5 are secreted molecules and 3 are membrane-type [2]. MT1-MMP or also known as MMP-14 is covalently linked to the cell membrane. &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3C7X&#039; size=&#039;400&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;PBD file obtained from http://pdb.org/pdb/explore/explore.do?structureId=3C7X &#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
More information on MMPs can be found on proteopedia at [[MMP]].&lt;br /&gt;
&lt;br /&gt;
==Inhibition==&lt;br /&gt;
&lt;br /&gt;
Tissue inhibitors of metalloproteinases (TIMPs)  are small molecules that can regulate the activity of MMPs. &amp;lt;scene name=&#039;56/567281/2/1&#039;&amp;gt;TIMP-2&amp;lt;/scene&amp;gt; is capable of binding the &amp;lt;scene name=&#039;56/567281/2/2&#039;&amp;gt;catalytic domain&amp;lt;/scene&amp;gt; of MMP-14, creating a new cell surface &amp;lt;scene name=&#039;56/566496/Timp1_bind_mmp1/1&#039;&amp;gt;molecule&amp;lt;/scene&amp;gt; involved in the activation of MMP-2 [3].&lt;br /&gt;
&lt;br /&gt;
==Extracellular Matrix Components==&lt;br /&gt;
MMP-14 degrades the following substrates in the extracellular matrix [2]:&lt;br /&gt;
:Aggrecan&lt;br /&gt;
:Collagen I&lt;br /&gt;
:Collagen II&lt;br /&gt;
:Collagen III&lt;br /&gt;
:Entactin/Nidogen&lt;br /&gt;
:Fibrillin&lt;br /&gt;
:Fibronectin&lt;br /&gt;
:Gelatin I&lt;br /&gt;
:Laminin&lt;br /&gt;
:Vitronectin&lt;br /&gt;
:α2-M&lt;br /&gt;
:α1-PI&lt;br /&gt;
:Factor XII&lt;br /&gt;
:Fibrin&lt;br /&gt;
:Fibrinogen&lt;br /&gt;
:ProMMP2&lt;br /&gt;
:ProTNFα&lt;br /&gt;
&lt;br /&gt;
==My Research Interest==&lt;br /&gt;
&lt;br /&gt;
In the [http://www.peytonlab.org/ Peyton Lab] I work to combine materials science with stem cell and cancer biology to design &#039;&#039;in vitro&#039;&#039; model biomaterial systems to understand cell motility. My project aims to design 3D biomaterial tissue mimics using poly(ethylene glycol). I incorporate degradable MMP crosslinkers into these biomaterials to allow cells the opportunity to move throughout the matrix and remodel their surrounding microenvironment.&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&lt;br /&gt;
[1]  L. Coussens, et al., Matrix Metalloproteinase Inhibitors and Cancer: Trials and Tribulations, Science, 2002. 295: p. 2387-92&lt;br /&gt;
&lt;br /&gt;
[2] M. Sternlicht, et al., How Matrix Metalloproteinases Regulate Cell Behavior,  Annu Rev Cell Dev Biol,  2001. 17: p. 463–516.&lt;br /&gt;
&lt;br /&gt;
[3] Egeblad, et. al., New Functions for the Matrix Metalloproteinases in Cancer Progression, Nat. Rev. Can., 2002, 2: 162-74&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/MMP14&amp;diff=1861714</id>
		<title>Molecular Playground/MMP14</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/MMP14&amp;diff=1861714"/>
		<updated>2013-11-06T21:42:09Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: /* Inhibition */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
MMp-14 allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&amp;quot;&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
Membrane Type 1 Matrix Metalloproteinase (MT1-MMP) is 1 of ~24 members of the MMP family of endopeptidases.  MMPs are zinc dependent proteinases that are capable of degrading virtually any extracellular matrix component [1].  Inherently, this enables MMPs to be a key player in regulation of cell behavior.  There are 8 structure classes for MMPs and of these classes,  5 are secreted molecules and 3 are membrane-type [2]. MT1-MMP or also known as MMP-14 is covalently linked to the cell membrane. &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3C7X&#039; size=&#039;400&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;PBD file obtained from http://pdb.org/pdb/explore/explore.do?structureId=3C7X &#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
More information on MMPs can be found on proteopedia at [[MMP]].&lt;br /&gt;
&lt;br /&gt;
==Inhibition==&lt;br /&gt;
&lt;br /&gt;
Tissue inhibitors of metalloproteinases (TIMPs)  are small molecules that can regulate the activity of MMPs. A unique  relationship exists between &amp;lt;scene name=&#039;56/567281/2/1&#039;&amp;gt;TIMP-2&amp;lt;/scene&amp;gt;. TIMP-2 binds the &amp;lt;scene name=&#039;56/567281/2/2&#039;&amp;gt;catalytic domain&amp;lt;/scene&amp;gt; of MMP14, creating a new cell surface &amp;lt;scene name=&#039;56/566496/Timp1_bind_mmp1/1&#039;&amp;gt;molecule&amp;lt;/scene&amp;gt; involved in the activation of MMP-2 [3].&lt;br /&gt;
&lt;br /&gt;
==Extracellular Matrix Components==&lt;br /&gt;
MMP-14 degrades the following substrates in the extracellular matrix [2]:&lt;br /&gt;
:Aggrecan&lt;br /&gt;
:Collagen I&lt;br /&gt;
:Collagen II&lt;br /&gt;
:Collagen III&lt;br /&gt;
:Entactin/Nidogen&lt;br /&gt;
:Fibrillin&lt;br /&gt;
:Fibronectin&lt;br /&gt;
:Gelatin I&lt;br /&gt;
:Laminin&lt;br /&gt;
:Vitronectin&lt;br /&gt;
:α2-M&lt;br /&gt;
:α1-PI&lt;br /&gt;
:Factor XII&lt;br /&gt;
:Fibrin&lt;br /&gt;
:Fibrinogen&lt;br /&gt;
:ProMMP2&lt;br /&gt;
:ProTNFα&lt;br /&gt;
&lt;br /&gt;
==My Research Interest==&lt;br /&gt;
&lt;br /&gt;
In the [http://www.peytonlab.org/ Peyton Lab] I work to combine materials science with stem cell and cancer biology to design &#039;&#039;in vitro&#039;&#039; model biomaterial systems to understand cell motility. My project aims to design 3D biomaterial tissue mimics using poly(ethylene glycol). I incorporate degradable MMP crosslinkers into these biomaterials to allow cells the opportunity to move throughout the matrix and remodel their surrounding microenvironment.&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&lt;br /&gt;
[1]  L. Coussens, et al., Matrix Metalloproteinase Inhibitors and Cancer: Trials and Tribulations, Science, 2002. 295: p. 2387-92&lt;br /&gt;
&lt;br /&gt;
[2] M. Sternlicht, et al., How Matrix Metalloproteinases Regulate Cell Behavior,  Annu Rev Cell Dev Biol,  2001. 17: p. 463–516.&lt;br /&gt;
&lt;br /&gt;
[3] Egeblad, et. al., New Functions for the Matrix Metalloproteinases in Cancer Progression, Nat. Rev. Can., 2002, 2: 162-74&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
	<entry>
		<id>https://proteopedia.org/index.php?title=Molecular_Playground/MMP14&amp;diff=1861713</id>
		<title>Molecular Playground/MMP14</title>
		<link rel="alternate" type="text/html" href="https://proteopedia.org/index.php?title=Molecular_Playground/MMP14&amp;diff=1861713"/>
		<updated>2013-11-06T21:36:34Z</updated>

		<summary type="html">&lt;p&gt;Lauren Jansen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;One of the [[CBI Molecules]] being studied in the  [http://www.umass.edu/cbi/ University of Massachusetts Amherst Chemistry-Biology Interface Program] at UMass Amherst and on display at the [http://www.molecularplayground.org/ Molecular Playground].&lt;br /&gt;
Molecular Playground banner: &#039;&#039;&#039;&amp;quot;&lt;br /&gt;
MMp-14 allows for 3D &#039;&#039;in vitro&#039;&#039; cell migration&amp;quot;&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
Membrane Type 1 Matrix Metalloproteinase (MT1-MMP) is 1 of ~24 members of the MMP family of endopeptidases.  MMPs are zinc dependent proteinases that are capable of degrading virtually any extracellular matrix component [1].  Inherently, this enables MMPs to be a key player in regulation of cell behavior.  There are 8 structure classes for MMPs and of these classes,  5 are secreted molecules and 3 are membrane-type [2]. MT1-MMP or also known as MMP-14 is covalently linked to the cell membrane. &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;Structure load=&#039;3C7X&#039; size=&#039;400&#039; frame=&#039;true&#039; align=&#039;right&#039; caption=&#039;PBD file obtained from http://pdb.org/pdb/explore/explore.do?structureId=3C7X &#039; scene=&#039;Insert optional scene name here&#039; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
More information on MMPs can be found on proteopedia at [[MMP]].&lt;br /&gt;
&lt;br /&gt;
==Inhibition==&lt;br /&gt;
&lt;br /&gt;
Tissue inhibitors of metalloproteinases (TIMPs)  are small molecules that can regulate the activity of MMPs. A unique  relationship exists between &amp;lt;scene name=&#039;56/567281/2/1&#039;&amp;gt;TIMP-2&amp;lt;/scene&amp;gt; and MMP-14 where TIMP-2 binds the &amp;lt;scene name=&#039;56/567281/2/2&#039;&amp;gt;catalytic site&amp;lt;/scene&amp;gt; of MMP14 and creates a &amp;lt;scene name=&#039;56/566496/Timp1_bind_mmp1/1&#039;&amp;gt;structure&amp;lt;/scene&amp;gt; and activates MMP-2 [3].&lt;br /&gt;
&lt;br /&gt;
==Extracellular Matrix Components==&lt;br /&gt;
MMP-14 degrades the following substrates in the extracellular matrix [2]:&lt;br /&gt;
:Aggrecan&lt;br /&gt;
:Collagen I&lt;br /&gt;
:Collagen II&lt;br /&gt;
:Collagen III&lt;br /&gt;
:Entactin/Nidogen&lt;br /&gt;
:Fibrillin&lt;br /&gt;
:Fibronectin&lt;br /&gt;
:Gelatin I&lt;br /&gt;
:Laminin&lt;br /&gt;
:Vitronectin&lt;br /&gt;
:α2-M&lt;br /&gt;
:α1-PI&lt;br /&gt;
:Factor XII&lt;br /&gt;
:Fibrin&lt;br /&gt;
:Fibrinogen&lt;br /&gt;
:ProMMP2&lt;br /&gt;
:ProTNFα&lt;br /&gt;
&lt;br /&gt;
==My Research Interest==&lt;br /&gt;
&lt;br /&gt;
In the [http://www.peytonlab.org/ Peyton Lab] I work to combine materials science with stem cell and cancer biology to design &#039;&#039;in vitro&#039;&#039; model biomaterial systems to understand cell motility. My project aims to design 3D biomaterial tissue mimics using poly(ethylene glycol). I incorporate degradable MMP crosslinkers into these biomaterials to allow cells the opportunity to move throughout the matrix and remodel their surrounding microenvironment.&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&lt;br /&gt;
[1]  L. Coussens, et al., Matrix Metalloproteinase Inhibitors and Cancer: Trials and Tribulations, Science, 2002. 295: p. 2387-92&lt;br /&gt;
&lt;br /&gt;
[2] M. Sternlicht, et al., How Matrix Metalloproteinases Regulate Cell Behavior,  Annu Rev Cell Dev Biol,  2001. 17: p. 463–516.&lt;br /&gt;
&lt;br /&gt;
[3] Egeblad, et. al., New Functions for the Matrix Metalloproteinases in Cancer Progression, Nat. Rev. Can., 2002, 2: 162-74&lt;/div&gt;</summary>
		<author><name>Lauren Jansen</name></author>
	</entry>
</feed>