Difference between revisions of "Team:Lethbridge/Parts"

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<p class="text12">The N<i>ex</i>t <i>vivo</i> system is made up of >40 unique parts encoding both protein and RNA components. The main focus of our team this year was to submit all 38 TX-TL protein components to the registry as a <a href="https://2017.igem.org/wiki/index.php?title=Team:Lethbridge/Part_Collection">collection of parts</a> that anyone could use to produce their own N<i>ex</i>t <i>vivo</i> system. Several of these TX-TL components were already in the registry but were under different expression control, lacked purification tags, and/or were not codon optimized for expression in <i>E. coli</i>. As such we sought to <a href="https://2017.igem.org/Team:Lethbridge/Improve">improve these parts</a> for future use.
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<p class="text12">The N<i>ex</i>t <i>vivo</i> system is made up of >40 unique parts encoding both protein and RNA components. The main focus of our team this year was to submit all 38 TX-TL protein components to the registry as a <a href="https://2017.igem.org/wiki/index.php?title=Team:Lethbridge/Part_Collection" id="pageLink">collection of parts</a> that anyone could use to produce their own N<i>ex</i>t <i>vivo</i> system. Several of these TX-TL components were already in the registry but were under different expression control, lacked purification tags, and/or were not codon optimized for expression in <i>E. coli</i>. As such we sought to <a href="https://2017.igem.org/Team:Lethbridge/Improve" id="pageLink">improve these parts</a> for future use.
 
</p>
 
</p>
  
<p class="text12">In addition to the TX-TL proteins, we also sought to BioBrick the ribosomal RNA genes and twenty tRNA genes. As a proof of concept for our novel tRNA purification design we only synthesized one representative tRNA gene before ordering them all. Additionally, the N<i>ex</i>t <i>vivo</i> system makes use of a previously submitted MS2BP part (<a href="http://parts.igem.org/Part:BBa_K2109108">BBA_K2109108</a>).
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<p class="text12">In addition to the TX-TL proteins, we also sought to BioBrick the ribosomal RNA genes and twenty tRNA genes. As a proof of concept for our novel tRNA purification design we only synthesized one representative tRNA gene before ordering them all. Additionally, the N<i>ex</i>t <i>vivo</i> system makes use of a previously submitted MS2BP part (<a href="http://parts.igem.org/Part:BBa_K2109108">BBA_K2109108 id="pageLink" />).
 
</p>
 
</p>
  
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             <h2 class="segmentHeader">Part Collection</h2>
 
             <h2 class="segmentHeader">Part Collection</h2>
  
<p class="text12">The <a href="https://2017.igem.org/wiki/index.php?title=Team:Lethbridge/Part_Collection">N<i>ex</i>t <i>vivo</i> part collection</a> consists of the 38 TX-TL proteins required for RNA transcription and protein synthesis. Each part in the collection has a hexahistidine tag for simultaneous purification of all components, the T7 promoter (<a href="http://partsregistry.org/Part:BBa_I719005">BBa_I719005</a>), medium RBS (<a href="http://parts.igem.org/Part:BBa_B0034">BBa_B0034</a>), and double terminator (<a href="http://parts.igem.org/Part:BBa_B0015">BBa_B0015</a>).
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<p class="text12">The <a href="https://2017.igem.org/wiki/index.php?title=Team:Lethbridge/Part_Collection" id="pageLink">N<i>ex</i>t <i>vivo</i> part collection</a> consists of the 38 TX-TL proteins required for RNA transcription and protein synthesis. Each part in the collection has a hexahistidine tag for simultaneous purification of all components, the T7 promoter (<a href="http://partsregistry.org/Part:BBa_I719005">BBa_I719005</a>), medium RBS (<a href="http://parts.igem.org/Part:BBa_B0034">BBa_B0034 id="pageLink" />), and double terminator (<a href="http://parts.igem.org/Part:BBa_B0015">BBa_B0015 id="pageLink" />).
 
</p>
 
</p>
 
   </div>
 
   </div>
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<div style="clear: both"></div>
 
<div style="clear: both"></div>
  
<p class="text12">This year we designed <a href="https://2017.igem.org/wiki/index.php?title=Team:Lethbridge/Composite_Part">41 composite parts</a>. Of the 41 parts, it contains 38 proteins essential for prokaryotic transcription and translation (TX-TL) as well 3 additional constructs for tRNA purification and TX-TL validation.</p>
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<p class="text12">This year we designed <a href="https://2017.igem.org/wiki/index.php?title=Team:Lethbridge/Composite_Part">41 composite parts id="pageLink" />. Of the 41 parts, it contains 38 proteins essential for prokaryotic transcription and translation (TX-TL) as well 3 additional constructs for tRNA purification and TX-TL validation.</p>
 
   
 
   
 
<div style="clear: both"></div>
 
<div style="clear: both"></div>
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<p>Basic parts paragraph.</p>
 
<p>Basic parts paragraph.</p>
<p><a href="https://2017.igem.org/wiki/index.php?title=Team:Lethbridge/Improve">Improved parts table</a></p>  </div>
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<p><a href="https://2017.igem.org/wiki/index.php?title=Team:Lethbridge/Improve" id="pageLink">Improved parts table</a></p>  </div>
 
     </div>
 
     </div>
 
<div style="clear: both"></div>
 
<div style="clear: both"></div>
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<p>All basic parts pages created on the registry of standard biological parts. Contains all 38 proteins essential for prokaryotic transcription and translation (Tx/Tl) as well as the parts for our tRNA purification and Tx/Tl validation construct.</p>
 
<p>All basic parts pages created on the registry of standard biological parts. Contains all 38 proteins essential for prokaryotic transcription and translation (Tx/Tl) as well as the parts for our tRNA purification and Tx/Tl validation construct.</p>
<p><a href="https://2017.igem.org/wiki/index.php?title=Team:Lethbridge/Basic_Part">Basic parts table</a>
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<p><a href="https://2017.igem.org/wiki/index.php?title=Team:Lethbridge/Basic_Part" id="pageLink">Basic parts table</a>
  
 
     </div>
 
     </div>

Revision as of 20:41, 29 October 2017





The Next vivo system is made up of >40 unique parts encoding both protein and RNA components. The main focus of our team this year was to submit all 38 TX-TL protein components to the registry as a collection of parts that anyone could use to produce their own Next vivo system. Several of these TX-TL components were already in the registry but were under different expression control, lacked purification tags, and/or were not codon optimized for expression in E. coli. As such we sought to improve these parts for future use.

In addition to the TX-TL proteins, we also sought to BioBrick the ribosomal RNA genes and twenty tRNA genes. As a proof of concept for our novel tRNA purification design we only synthesized one representative tRNA gene before ordering them all. Additionally, the Next vivo system makes use of a previously submitted MS2BP part (BBA_K2109108 id="pageLink" />).

Part Collection

The Next vivo part collection consists of the 38 TX-TL proteins required for RNA transcription and protein synthesis. Each part in the collection has a hexahistidine tag for simultaneous purification of all components, the T7 promoter (BBa_I719005), medium RBS (BBa_B0034 id="pageLink" />), and double terminator (BBa_B0015 id="pageLink" />).

Composite Parts

General Protein Construct





General RNA Construct






This year we designed 41 composite parts id="pageLink" />. Of the 41 parts, it contains 38 proteins essential for prokaryotic transcription and translation (TX-TL) as well 3 additional constructs for tRNA purification and TX-TL validation.

Basic Parts

All basic parts pages created on the registry of standard biological parts. Contains all 38 proteins essential for prokaryotic transcription and translation (Tx/Tl) as well as the parts for our tRNA purification and Tx/Tl validation construct.

Basic parts table