Team:UCLA

From 2013.igem.org

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<title>UCLA iGEM </title>
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<img src="https://static.igem.org/mediawiki/2013/e/ea/Grad.png" width="960">
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<p id="text"><a href="#slide2"><font color="white">How it Works</font></a><br>
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&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="#slide2"><img src="https://static.igem.org/mediawiki/2013/6/62/Downarrow.png" href="#slide2" width="50"></a></p>
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<p id="text2"><a href="#slide3"><font color="Black">mRNA Display</font></a><br>
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&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="#slide3"><img src="https://static.igem.org/mediawiki/2013/1/11/Down_arrow_black.png"Width="50">
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<center><a href="https://2013.igem.org/Team:UCLA"><img src="http://www.synbioatucla.com/logo.jpg" width=450></a></center>
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<a href="#slide1"><img src="https://static.igem.org/mediawiki/2013/c/c2/Uparrow_white.png" href="#slide2" width="50"></a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
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&nbsp;<a href="#slide1"><font color="white">Top</font></a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="https://2013.igem.org/Team:UCLA/Project"><font color="white">More Details!</font></a>
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<td><a href="https://2013.igem.org/Team:UCLA">
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<td><a href="https://2013.igem.org/Team:UCLA/Parts">
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<td><a href="https://2013.igem.org/Team:UCLA/Modeling">
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<td><a href="https://2013.igem.org/Team:UCLA/Notebook">
 
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<td><a href="https://2013.igem.org/Team:UCLA/Safety">
 
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<img src="https://static.igem.org/mediawiki/2013/c/c2/Safety_ucla.jpg" name="safety"  width=100%></a></td>
 
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<td><a href="https://2013.igem.org/Team:UCLA/Attributions">
 
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<img src="https://static.igem.org/mediawiki/2013/9/91/Attributions.jpg" name="attributions" width=100%></a></td>
 
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<img src="http://www.synbioatucla.com/home_pic1.jpg" width=400 style="float:left">
 
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<h1>UCLA's debut iGEM team!</h1>
 
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<p><b>DiversiPhage: Library Generation for Protein Selection</b></p>
 
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<p>Both the mammalian immune system’s complex defenses and a bacteriophage’s targeting mechanism depend upon protein diversification. These models have inspired innovations ranging from targeted drug delivery to protein display. Using the major tropism determining (MTD) protein expressed on the Bordatella bacteriophage BPP-1, we aim to develop an in vitro system for generating antibody-like proteins that bind specified targets. The MTD protein expressed at the phage’s tail fiber is naturally modified at its variable region to produce nearly 10<sup>13</sup> possible binding variants while preserving its structure. Mutating the MTD’s variable region by PCR can match the massive diversity of MTD in vitro. A library of MTD protein-DNA fusions generated by mRNA display can then be screened for binding against specified protein targets. This in vitro analog to phage display and immune clonal selection can be a powerful tool for constructing target-binding MTD variants with equally many varied applications.
 
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<p>As members of UCLA's Synthetic Biology Club and iGEM team, we are excited to see where the field of synthetic biology, and the iGEM competition, can take us!</p>
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UCLA's debut iGEM team!
 
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We're focusing on developing practical applications for diversity generating retroelements found in bacteria and bacteriophages.
 
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|align="center"|[[Team:UCLA | Team UCLA]]
 
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<!--- The Mission, Experiments --->
 
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<!--{| style="color:#1b2c8a;background-color:#0c6;" cellpadding="3" cellspacing="1" border="1" bordercolor="#fff" width="62%" align="center"
 
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!align="center"|[[Team:UCLA|Home]]
 
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!align="center"|[[Team:UCLA/Team|Team]]
 
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!align="center"|[https://igem.org/Team.cgi?year=2013&team_name=UCLA Official Team Profile]
 
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!align="center"|[[Team:UCLA/Project|Project]]
 
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!align="center"|[[Team:UCLA/Parts|Parts Submitted to the Registry]]
 
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!align="center"|[[Team:UCLA/Modeling|Modeling]]
 
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!align="center"|[[Team:UCLA/Notebook|Notebook]]
 
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!align="center"|[[Team:UCLA/Safety|Safety]]
 
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!align="center"|[[Team:UCLA/Attributions|Attributions]]
 
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Latest revision as of 21:11, 27 September 2013


UCLA iGEM

How it Works
       

mRNA Display
       

           
 Top       More Details!

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