Difference between revisions of "Part:BBa K5302022"
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We used pBBR plasmid as a backbone and transfered V114 into Escherichia coli Nissle 1917, and finally succeeded in expressing V114. | We used pBBR plasmid as a backbone and transfered V114 into Escherichia coli Nissle 1917, and finally succeeded in expressing V114. | ||
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+ | <img src="https://static.igem.wiki/teams/5302/images/part-registry-pov114-1.png" | ||
+ | width="60%" style="display:block; margin:auto;" alt="Jamboree Program" > | ||
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+ | <b>Figure 1. </b> Colony PCR results of pBBR-OmpA-V114 | ||
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<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 10:10, 1 October 2024
pBBR-OmpA-V114
v114 has been identified as a small potent VEGF-binding peptide, which is composed of 8 amino acids--- that is VEPNc[CDIHVnLWEWEC]FERL, and there is a disulfide bond between N and F, making the stucture more stable. This peptide has a similiar structure and VEGF-binding site as V107, and it shows great affinity with VEGF(Kd=0.11 μM).
We used pBBR plasmid as a backbone and transfered V114 into Escherichia coli Nissle 1917, and finally succeeded in expressing V114.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 3979
Illegal XbaI site found at 3140
Illegal PstI site found at 1967
Illegal PstI site found at 3128 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 3979
Illegal PstI site found at 1967
Illegal PstI site found at 3128
Illegal NotI site found at 1008 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 3979
Illegal BglII site found at 1754
Illegal BamHI site found at 3146 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 3979
Illegal XbaI site found at 3140
Illegal PstI site found at 1967
Illegal PstI site found at 3128 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 3979
Illegal XbaI site found at 3140
Illegal PstI site found at 1967
Illegal PstI site found at 3128
Illegal NgoMIV site found at 2418
Illegal NgoMIV site found at 2701
Illegal NgoMIV site found at 4637
Illegal AgeI site found at 4477 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1330
Illegal SapI.rc site found at 2267
Illegal SapI.rc site found at 2477