Difference between revisions of "Team:Pittsburgh/Collaborations"

 
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<h2>Contents</h2>
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    <p>Our work with other teams</p></div>
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    <div class="table column full_size" style="padding-top:0;">
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<h2 style="color:#1c2957; padding-top:0;">Contents</h2>
 
<ul class="table">
 
<ul class="table">
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<li><a href="#WM" class="table">William and Mary</a></li>
 
<li><a href="#WM" class="table">William and Mary</a></li>
 
<li><a href="#UGA" class="table">University of Georgia</a></li>
 
<li><a href="#UGA" class="table">University of Georgia</a></li>
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<li><a href="#surveys" class="table">Surveys</a></li>
 
<li><a href="#UMD" class="table">Mid-Atlantic Meet-Up</a></li>
 
<li><a href="#UMD" class="table">Mid-Atlantic Meet-Up</a></li>
 
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<h1 class="nav"><a name="UMD" class="nav">Mid-Atlantic Meet-Up</a></h1>
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<p>On July 22, Claire, Praneeth, and Maya visited the University of Maryland to participate in the Second Annual Mid-Atlantic iGEM Conference. They had a great time meeting fellow iGEM'ers, discussing synthetic biology, and exploring College Park and Washington D.C. Thanks to the <a href="https://2016.igem.org/Team:UMaryland" target="_blank"> UMaryland team</a> for organizing such a great event and for being awesome hosts! Take a look at the slideshow presentation <a href="https://static.igem.org/mediawiki/2016/e/e9/T--Pittsburgh--CollabUMD.pdf" target="_blank">here</a>.</p>
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<span class="anchor" id="WM"></span>  
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<h1>William and Mary: Circuit Control Toolbox</h1>
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    <p>The <a href="https://2016.igem.org/Team:William_and_Mary" target="_blank">William & Mary team</a> is developing a toolbox of parts that can be easily integrated into genetic circuits to tune the resulting levels of protein expression. They characterize their parts exclusively in <i>E. coli</i>. We tested eight of their toolbox parts in Promega's S30 Extract System for Circular DNA to compare the behavior of the parts in cells versus <i>in vitro</i>. The eight plasmids had different RBS strengths, which are reflected in our data shown below. Learn more about the experiments we performed and the results by reading our <a href="https://static.igem.org/mediawiki/2016/4/46/T--Pittsburgh--CollaborationsWM_report.pdf" target="_blank">report</a>.</p>
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    <img src="https://static.igem.org/mediawiki/2016/7/7c/T--Pittsburgh--CollaborationsWM_graph.jpg" alt="results" style="width:50%; display:block; margin:auto;">
 
<a href="#Top">Back to Top</a>
 
<a href="#Top">Back to Top</a>
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<h1>University of Georgia: Archaeal InterLab</h1>
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    <p>The <a href="https://2016.igem.org/Team:UGA-Georgia" target="_blank">UGA team</a> is developing an mCherry library for <i>Methanococcus maripaludis</i>, an archaeal organism. Their library currently contains over 30 mutations in the RBS, which cause different levels of protein expression. We took fluorescence readings for several of these mutations as part of the "Archaeal InterLab." Like iGEM's InterLab Study, which aims to standardize fluorescence readings across all machines, the Archaeal InterLab recognizes that fluorescence lacks an absolute unit. Thus, participating teams record the relative fluorescence of the cells containing various RBS mutations for UGA.</p>
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<p>This page is used by the judges to evaluate your team for the <a href="https://2016.igem.org/Judging/Medals">team collaboration silver medal criterion</a>. </p>
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    <p>We were given five samples: three mutants (A, B, and C), a wild type (WT), and suspension buffer (S). Each of the samples was read in triplicate. Here are our average fluorescence readings for each sample. Error bars represent standard deviation. For more detailed protocols, notes, and data, visit our <a href="https://static.igem.org/mediawiki/2016/9/9f/T--Pittsburgh--NotebookWeek11.pdf" target="_blank"> Week 11 Lab Notebook</a>.</p>
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    <img src="https://static.igem.org/mediawiki/2016/3/3f/T--Pittsburgh--CollaborationsUGAgraph.jpg" style="width:60%; display:block; margin: 0 auto;"  alt="Results">
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<p> Delete this box in order to be evaluated for this medal. See more information at <a href="https://2016.igem.org/Judging/Evaluated_Pages/Instructions"> Instructions for Evaluated Pages </a>.</p>
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<h1>Surveys</h1>   
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<p>Our team worked with team <a href="https://2016.igem.org/Team:Tianjin" target="_blank"> Tianjin</a> and other collaborators to create a survey about the use of synthetic biology to solve environmental problems. We also participated in surveys distributed by teams <a href="https://2016.igem.org/Team:Evry" target="_blank">Evry</a> and <a href="https://2016.igem.org/Team:LMU-TUM_Munich" target="_blank">Munich</a>. </p>
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    <h1 style="clear:both;">Mid-Atlantic Meet-Up</h1>
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<p>On July 22, Claire, Praneeth, and Maya visited the University of Maryland to participate in the Second Annual Mid-Atlantic iGEM Conference. They had a great time meeting fellow iGEM'ers, learning about other teams' projects, and discussing synthetic biology. They also explored College Park and the National Portrait Gallery in Washington D.C. with members of the UMaryland team. Thanks to the <a href="https://2016.igem.org/Team:UMaryland" target="_blank"> UMaryland team</a> for organizing such a great event and for being awesome hosts! Take a look at our presentation slides <a href="https://static.igem.org/mediawiki/2016/e/e9/T--Pittsburgh--CollabUMD.pdf" target="_blank">here</a>.</p>
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Latest revision as of 02:06, 19 October 2016

Thank you to our sponsors!

Office of the Provost Department of Bioengineering Department of Biological Sciences Department of Chemistry Swanson School of Engineering
IDT NEB Experiment

Our work with other teams

Contents

William and Mary: Circuit Control Toolbox

The William & Mary team is developing a toolbox of parts that can be easily integrated into genetic circuits to tune the resulting levels of protein expression. They characterize their parts exclusively in E. coli. We tested eight of their toolbox parts in Promega's S30 Extract System for Circular DNA to compare the behavior of the parts in cells versus in vitro. The eight plasmids had different RBS strengths, which are reflected in our data shown below. Learn more about the experiments we performed and the results by reading our report.

results Back to Top

University of Georgia: Archaeal InterLab

The UGA team is developing an mCherry library for Methanococcus maripaludis, an archaeal organism. Their library currently contains over 30 mutations in the RBS, which cause different levels of protein expression. We took fluorescence readings for several of these mutations as part of the "Archaeal InterLab." Like iGEM's InterLab Study, which aims to standardize fluorescence readings across all machines, the Archaeal InterLab recognizes that fluorescence lacks an absolute unit. Thus, participating teams record the relative fluorescence of the cells containing various RBS mutations for UGA.

We were given five samples: three mutants (A, B, and C), a wild type (WT), and suspension buffer (S). Each of the samples was read in triplicate. Here are our average fluorescence readings for each sample. Error bars represent standard deviation. For more detailed protocols, notes, and data, visit our Week 11 Lab Notebook.

Results Back to Top

Surveys

Our team worked with team Tianjin and other collaborators to create a survey about the use of synthetic biology to solve environmental problems. We also participated in surveys distributed by teams Evry and Munich.

Back to Top

Mid-Atlantic Meet-Up

presentation
Presenting our work
group photo
The participants
team photo
Team Pittsburgh
discussion
Discussion session
Capitol
U.S. Capitol
Supreme Court
Supreme Court building
National Portrait Gallery courtyard
Kogod Courtyard

On July 22, Claire, Praneeth, and Maya visited the University of Maryland to participate in the Second Annual Mid-Atlantic iGEM Conference. They had a great time meeting fellow iGEM'ers, learning about other teams' projects, and discussing synthetic biology. They also explored College Park and the National Portrait Gallery in Washington D.C. with members of the UMaryland team. Thanks to the UMaryland team for organizing such a great event and for being awesome hosts! Take a look at our presentation slides here.

Back to Top