Difference between revisions of "Team:NCTU Formosa/Composite Part"

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<h2> Composite Parts</h2>
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<h4>Note</h4>
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ins {
<p>In order to be considered for the <a href="https://2015.igem.org/Judging/Awards#SpecialPrizes">Best New Composite Part award</a>, you must fill out this page. Please give links to the Registry entries for the Composite parts you have made. Please see the Registry's <a href="http://parts.igem.org/Help:Parts#Basic_and_Composite_Parts"> Help:Parts page</a> for more information on part types.</p>
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<div class="title">Composite Parts</div>
 
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<h2>Composite Part</h2>
  
<p>
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<table>  
A composite part is a functional unit of DNA consisting of two or more basic parts assembled together. <a href="http://parts.igem.org/wiki/index.php/Part:BBa_I13507">BBa_I13507</a> is an example of a composite part, consisting of an RBS, a protein coding region for a red fluorescent protein, and a terminator.
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  <tr><td width="20%"></td><td width="13%"></td><td width="67%"></td></tr>  
</p>
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<p>New composite BioBrick devices can be made by combining existing BioBrick Parts (like Inverters, Amplifiers, Smell Generators, Protein Balloon Generators, Senders, Receivers, Actuators, and so on).</p>
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  <tr><td class="part"><span><a href="http://parts.igem.org/Part:BBa_K1694013">BBa_K1694013</a></span><br>
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                                  OmpA-anti-VEGF<br>
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                      <span><a href="http://parts.igem.org/Part:BBa_K1694014">BBa_K1694014</a></span><br>
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                                OmpA-anti-EGFR<br>
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                      <span><a href="http://parts.igem.org/Part:BBa_K1694015">BBa_K1694015</a></span><br>
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                                OmpA-anti-HER2<br>
 +
</td><td></td><td>In order to change the scFv parts easily, we added a <i>Nco</i>I restriction site between OmpA and scFv so that we can change various scFv DNA sequence using the <i>Nco</i>I restriction enzyme.</td></tr>  
  
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<tr><td class="part"><span><a href="http://parts.igem.org/Part:BBa_K1694023">BBa_K1694023</a></span><br>
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                                  P<sub>cons</sub>+RBS+OmpA-anti-VEGF<br>
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                      <span><a href="http://parts.igem.org/Part:BBa_K1694024">BBa_K1694024</a></span><br>
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                                P<sub>cons</sub>+RBS+OmpA-anti-EGFR<br>
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                      <span><a href="http://parts.igem.org/Part:BBa_K1694025">BBa_K1694025</a></span><br>
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                                P<sub>cons</sub>+RBS+OmpA-anti-HER2<br>
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</td><td></td><td>By ligating the constitutive promoter (<a href="http://parts.igem.org/Part:BBa_J23101">BBa_J23101</a>), strong ribosome binding site (<a href="http://parts.igem.org/Part:BBa_B0034">BBa_B0034</a>) and Lpp-OmpA-scFv, we were able to display scFv on the <i>E.coli</i> outer membrane continuously.
 +
Having this part, we can co-transform with other parts in order to produce color as the detection signal.<br><br>
  
 +
In addition, by co-transforming these different types of <i>E.coli</i> with different fluorescence or color as signals, we are able to create a platform which can detect multimarker and consequently achieve combination therapy.
 +
</td></tr>
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<tr><td class="part"><span><a href="http://parts.igem.org/Part:BBa_K1694033">BBa_K1694033</a></span><br>
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                                  P<sub>cons</sub>+RBS+OmpA-anti-VEGF+RBS+GFP+Ter<br>
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                      <span><a href="http://parts.igem.org/Part:BBa_K1694034">BBa_K1694034</a></span><br>
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                                P<sub>cons</sub>+RBS+OmpA-anti-EGFR+RBS+GFP+Ter<br>
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                      <span><a href="http://parts.igem.org/Part:BBa_K1694035">BBa_K1694035</a></span><br>
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                                P<sub>cons</sub>+RBS+OmpA-anti-HER2+RBS+GFP+Ter<br>
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                      <span><a href="http://parts.igem.org/Part:BBa_K1694044">BBa_K1694044</a></span><br>
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                      Pcons+RBS+OmpA-anti-EGFR+RBS+RFP+Ter<br>
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                      <span><a href="http://parts.igem.org/Part:BBa_K1694045">BBa_K1694045</a></span><br>
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                                P<sub>cons</sub>+RBS+OmpA-anti-HER2+RBS+BFP+Ter<br>
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</td><td></td><td>The most commonly constructing way of composite parts is to ligate the required parts together. We also provide this kind of parts.<br>
 +
At the back of the Lpp-OmpA-scFv part, we ligated the weaker ribosome biding site (<a href="網址">BBa_B0030</a>), different fluorescent protein and terminator (<a href="http://parts.igem.org/Part:BBa_J61048">BBa_J61048</a>) to make it continuously and simultaneously express the fluorescence and the scFv. We used a weak ribosome binding site to ensure that scFv's production will not be affected.
 +
</td></tr>
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<tr><td class="part"><span><a href="http://parts.igem.org/Part:BBa_K1694053">BBa_K1694053</a></span><br>
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                                  P<sub>cons</sub>+RBS+OmpA-anti-VEGF+RBS+amilCP+Ter<br>
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                      <span><a href="http://parts.igem.org/Part:BBa_K1694054">BBa_K1694054</a></span><br>
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                                P<sub>cons</sub>+RBS+OmpA-anti-EGFR+RBS+amilCP+Ter<br>
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                      <span><a href="http://parts.igem.org/Part:BBa_K1694055">BBa_K1694055</a></span><br>
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                                P<sub>cons</sub>+RBS+OmpA-anti-HER2+RBS+amilCP+Ter<br>
 +
</td><td></td><td>Chromoprotein is another example of what can be added when making your own probe.<br>
 +
We constructed this part as the P<sub>cons</sub>+RBS+OmpA-scFv+RBS+fluorescent protein+Terminator part.
 +
</td></tr>
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<tr><td class="part"><span><a href="http://parts.igem.org/Part:BBa_K1694027">BBa_K1694027</a></span><br>
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                                  P<sub>cons</sub>+RBS+FadL-GBP<br>
 +
</td><td></td><td>By ligating the induced promoter (<a href="http://parts.igem.org/Part:BBa_J23110">BBa_J23110</a>), ribosome binding site (<a href="http://parts.igem.org/Part:BBa_B0034">BBa_B0034</a>) and FadL-GBP, we can continuously display the GBP on the <i>E.coli</i> outer membrane.<br>
 +
Then we co-transform the OmpA-scFv parts and this FadL-GBP parts into the same <i>E.coli</i>, hence allowing our <i>E.coli</i> to bind on gold chips and detect antigens simultaneously.
 +
</td></tr>
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<tr><td class="part"><span><a href="http://parts.igem.org/Part:BBa_K1694037">BBa_K1694037</a></span><br>
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                                P<sub>cons</sub>+RBS+FadL-GBP+RBS+GFP+Ter<br>
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</td><td></td><td>With this part, we can test the GBP function by observing the green fluorescence on the gold chip. Terminator  is (<a href="http://parts.igem.org/Part:BBa_B0015">BBa_B0015</a>).
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</td></tr>
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</table>
 
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{{Team:NCTU_Formosa/footer}}

Latest revision as of 03:58, 19 September 2015

Composite Parts

Composite Part

BBa_K1694013
OmpA-anti-VEGF
BBa_K1694014
OmpA-anti-EGFR
BBa_K1694015
OmpA-anti-HER2
In order to change the scFv parts easily, we added a NcoI restriction site between OmpA and scFv so that we can change various scFv DNA sequence using the NcoI restriction enzyme.
BBa_K1694023
Pcons+RBS+OmpA-anti-VEGF
BBa_K1694024
Pcons+RBS+OmpA-anti-EGFR
BBa_K1694025
Pcons+RBS+OmpA-anti-HER2
By ligating the constitutive promoter (BBa_J23101), strong ribosome binding site (BBa_B0034) and Lpp-OmpA-scFv, we were able to display scFv on the E.coli outer membrane continuously. Having this part, we can co-transform with other parts in order to produce color as the detection signal.

In addition, by co-transforming these different types of E.coli with different fluorescence or color as signals, we are able to create a platform which can detect multimarker and consequently achieve combination therapy.
BBa_K1694033
Pcons+RBS+OmpA-anti-VEGF+RBS+GFP+Ter
BBa_K1694034
Pcons+RBS+OmpA-anti-EGFR+RBS+GFP+Ter
BBa_K1694035
Pcons+RBS+OmpA-anti-HER2+RBS+GFP+Ter
BBa_K1694044
Pcons+RBS+OmpA-anti-EGFR+RBS+RFP+Ter
BBa_K1694045
Pcons+RBS+OmpA-anti-HER2+RBS+BFP+Ter
The most commonly constructing way of composite parts is to ligate the required parts together. We also provide this kind of parts.
At the back of the Lpp-OmpA-scFv part, we ligated the weaker ribosome biding site (BBa_B0030), different fluorescent protein and terminator (BBa_J61048) to make it continuously and simultaneously express the fluorescence and the scFv. We used a weak ribosome binding site to ensure that scFv's production will not be affected.
BBa_K1694053
Pcons+RBS+OmpA-anti-VEGF+RBS+amilCP+Ter
BBa_K1694054
Pcons+RBS+OmpA-anti-EGFR+RBS+amilCP+Ter
BBa_K1694055
Pcons+RBS+OmpA-anti-HER2+RBS+amilCP+Ter
Chromoprotein is another example of what can be added when making your own probe.
We constructed this part as the Pcons+RBS+OmpA-scFv+RBS+fluorescent protein+Terminator part.
BBa_K1694027
Pcons+RBS+FadL-GBP
By ligating the induced promoter (BBa_J23110), ribosome binding site (BBa_B0034) and FadL-GBP, we can continuously display the GBP on the E.coli outer membrane.
Then we co-transform the OmpA-scFv parts and this FadL-GBP parts into the same E.coli, hence allowing our E.coli to bind on gold chips and detect antigens simultaneously.
BBa_K1694037
Pcons+RBS+FadL-GBP+RBS+GFP+Ter
With this part, we can test the GBP function by observing the green fluorescence on the gold chip. Terminator is (BBa_B0015).