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

Revision as of 19:56, 18 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 P_cons+RBS+OmpA-anti-VEGF BBa_K1694024 P_cons+RBS+OmpA-anti-EGFR BBa_K1694025 P_cons+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 P_cons+RBS+OmpA-anti-VEGF+RBS+GFP+Ter BBa_K1694034 P_cons+RBS+OmpA-anti-EGFR+RBS+GFP+Ter BBa_K1694035 P_cons+RBS+OmpA-anti-HER2+RBS+GFP+Ter BBa_K1694044 Pcons+RBS+OmpA-anti-EGFR+RBS+RFP+Ter BBa_K1694045 P_cons+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 P_cons+RBS+OmpA-anti-VEGF+RBS+amilCP+Ter BBa_K1694054 P_cons+RBS+OmpA-anti-EGFR+RBS+amilCP+Ter BBa_K1694055 P_cons+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 P_cons+RBS+OmpA-scFv+RBS+fluorescent protein+Terminator part.
BBa_K1694027 P_induce+RBS+FadL-GBP		By ligating the induced promoter (BBa_R0010), 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 P_induce+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),

Reference
[1] C Hartmann et al. (2010) Peptide mimotopes recognized by antibodies cetuximab and matuzumab induce a functionally equivalent anti-EGFR immune response
[2] DrugBank: Bevacizumab (DB00112)
[3] DrugBank: Cetuximab (DB00002)
[4] DrugBank: Trastuzumab (DB00072)
[5] Tae Jung Park et al. (2009) Development of a whole-cell biosensor by cell surface display of a gold-binding polypeptide on the gold surface

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NCTU_Formosa APOllO

National Chaio Tung University
Engineering Building 6 EF455, 1001 University Road, Hsinchu 300, Taiwan, ROC.

@@ Line 202: / Line 202: @@
                         <span><a href="http://parts.igem.org/Part:BBa_K1694025">BBa_K1694025</a></span><br>
                                  P<sub>cons</sub>+RBS+OmpA-anti-HER2<br>
-</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.
+</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>
@@ Line 235: / Line 235: @@
 <tr><td class="part"><span><a href="http://parts.igem.org/Part:BBa_K1694027">BBa_K1694027</a></span><br>
                                    P<sub>induce</sub>+RBS+FadL-GBP<br>
-</td><td></td><td>By ligating the induced promoter (<a href="http://parts.igem.org/Part:BBa_R0010">BBa_R0010</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>
+</td><td></td><td>By ligating the induced promoter (<a href="http://parts.igem.org/Part:BBa_R0010">BBa_R0010</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.
+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>