Difference between revisions of "Team:Minnesota/Modeling"

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{{Minnesota}}
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<h2> Modeling</h2>
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<div class="highlightBox">
 
<h4>Note</h4>
 
<p>In order to be considered for the <a href="https://2015.igem.org/Judging/Awards#SpecialPrizes">Best Model award</a>, you must fill out this page.</p>
 
</div>
 
  
  
<p>Mathematical models and computer simulations provide a great way to describe the function and operation of BioBrick Parts and Devices. Synthetic Biology is an engineering discipline, and part of engineering is simulation and modeling to determine the behavior of your design before you build it. Designing and simulating can be iterated many times in a computer before moving to the lab. This award is for teams who build a model of their system and use it to inform system design or simulate expected behavior in conjunction with experiments in the wetlab.</p>
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                class='selected'       ><a href="/Team:Minnesota/Project/Insulin">Page              </a></li>
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                class='new'       ><a href="/wiki/index.php?title=Talk:Team:Minnesota/Project/Insulin&amp;action=edit&amp;redlink=1">Discussion              </a></li>
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              <li
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                    ><a href="/wiki/index.php?title=Team:Minnesota/Project/Insulin&amp;action=edit">View source              </a></li>
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              <li
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                    ><a href="/wiki/index.php?title=Team:Minnesota/Project/Insulin&amp;action=history">History              </a></li>
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Here are a few examples from previous teams:
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<!---START HERE--->
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<h1> 2A Viral Tag Modeling for Biosynthesis </h1><br>
 +
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<i> &nbsp; &nbsp; &nbsp; &nbsp;  Building a 2A eukaryotic biochemical network can be hard, and these viral tags are not without a drawback. Previous research (Beekwilder 2014) has shown there was a decreased level of expression of enzymes downstream of the promoter. This can certainly affect the overall yield of the pathway, but we can certainly minimize this effect!
 +
</i><br><br>
 +
 +
 +
<br>
 +
&nbsp; &nbsp; &nbsp; &nbsp; We have designed a computation tool to combinatorically test all available rearrangements of your biochemical network and display the ideal ordering of your network to optimize reaction efficiency. The model utilizes the heavily studied kinetics of enzymes and implements their behavior in a differential equations model. This is nested within a permutation loop to test all possible orderings.
 +
<br><br>
 +
<br>
 +
 +
<center><i> To prove how easy it is to use, we even redesigned three 2014 iGEM teams circuits for how they would be optimally arranged in eukaryotic 2A systems! </center></i><br><br>
 +
 +
 +
 +
<center> <b> 2014 Arizona State Pyruvate to Fatty Acid Ethyl Esters </b></center><br>
 +
 +
<center> Promoter -> pyruvate dehydrogenase (1st)-> Long-chain acyl-ACP reductase (2nd) -> Alcohol dehydrogenase (3rd) -> Long-chain-fatty-acid-CoA ligase EC (4th) </center><br><br>
 +
 +
                             
 +
 +
<center> <b> 2014 BYU Denitrification </b></center><br>
 +
 +
<center> Promoter -> Nitrite reductase (1st) -> Nitrous-oxide reductase (2nd) -> Nitric Oxide reductase (3rd) ></center><br><br>
 +
 +
 +
 +
<center> <b> 2014UIUC caffeine degradation for dogs </b></center><br>
 +
 +
Promoter -> 7-methylxanthine demethylase (1st)-> Methylxanthine N1-demethylase (2nd) -> Methylxanthine N1-demethylase (3rd) ></center><br><br><br>
 +
 +
&nbsp; &nbsp; &nbsp; &nbsp; To emphasize the portability of this tool, the system was designed in MATLAB and embedded in a graphical user interface (GUI). If you want to test this tool out or use it to optimize your own experiments, head on over to:
 +
 +
 +
<br><br><center>https://github.com/PatrickHolec/Pathway2A</center><br>
 +
<center>or contact:</center><br>
 +
<center>Patrick V. Holec</center>
 +
<center>hole0077@umn.edu</center>
 +
<center>University of Minnesota</center><br>
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Latest revision as of 03:52, 19 September 2015

Team:Minnesota/Project/Insulin - 2015.igem.org

 

Team:Minnesota/Project/Insulin

From 2015.igem.org

Team:Minnesota - Main Style Template Team:Minnesota - Template

2A Viral Tag Modeling for Biosynthesis


        Building a 2A eukaryotic biochemical network can be hard, and these viral tags are not without a drawback. Previous research (Beekwilder 2014) has shown there was a decreased level of expression of enzymes downstream of the promoter. This can certainly affect the overall yield of the pathway, but we can certainly minimize this effect!


        We have designed a computation tool to combinatorically test all available rearrangements of your biochemical network and display the ideal ordering of your network to optimize reaction efficiency. The model utilizes the heavily studied kinetics of enzymes and implements their behavior in a differential equations model. This is nested within a permutation loop to test all possible orderings.


To prove how easy it is to use, we even redesigned three 2014 iGEM teams circuits for how they would be optimally arranged in eukaryotic 2A systems!


2014 Arizona State Pyruvate to Fatty Acid Ethyl Esters

Promoter -> pyruvate dehydrogenase (1st)-> Long-chain acyl-ACP reductase (2nd) -> Alcohol dehydrogenase (3rd) -> Long-chain-fatty-acid-CoA ligase EC (4th)


2014 BYU Denitrification

Promoter -> Nitrite reductase (1st) -> Nitrous-oxide reductase (2nd) -> Nitric Oxide reductase (3rd) >


2014UIUC caffeine degradation for dogs

Promoter -> 7-methylxanthine demethylase (1st)-> Methylxanthine N1-demethylase (2nd) -> Methylxanthine N1-demethylase (3rd) >


        To emphasize the portability of this tool, the system was designed in MATLAB and embedded in a graphical user interface (GUI). If you want to test this tool out or use it to optimize your own experiments, head on over to:

https://github.com/PatrickHolec/Pathway2A

or contact:

Patrick V. Holec
hole0077@umn.edu
University of Minnesota