Plasmid

Part:BBa_K5302016

Designed by: Xinyuan Shi   Group: iGEM24_USTC   (2024-10-01)


pBBR-OmpA-VEGFR1D2

This work is derived from pBBR-OmpA-mCherry and pUC19-VEGFR1D2, and it has undergone codon optimization. This composite part combines OmpA(21.4kda) and VEGFR1D2(approximately 12kda), we succeeded in transferring this plasmid into Escherichia coli Nissle 1917 and let it express VEGFR1D2. The plasmid uses lac promotor and has kanamycin resistence.

Jamboree Program
Figure 1. Colony PCR results of pBBR-OmpA-VEGFR1D2


VEGF binds to two tyrosine kinase receptors, VEGF receptor 1 (VEGFR1/Flt-1) and receptor 2 (VEGFR2/KDR), which are localized on the cell surface of various cell types. The receptors are organized in two intracellular kinase domains, a short transmembrane region and an extracellular portion constituted of seven immunoglobulin-like domains. The binding of VEGF to the extracellular domain induces receptor dimerization, transphosphorylation of the kinase domains, and activation of the intracellular signaling. Deletion studies have shown that the ligand binding function resides within the first three domains of VEGFR14 and in domains 2 and 3 of VEGFR2. Deletion of the second extracellular domain of VEGFR1 (VEGFR1D2) completely abolishes the binding to VEGF, whereas VEGFR1D2 binds VEGF with an affinity that is only 60 times lower than the entire extracellular portion of the receptor. The equilibrium constant for the binding of VEGF to one VEGFR1D2 molecule was determined by surface plasmon resonance. The obtained value, 2.9 ± 0.2 nM, is consistent with the constant reported for the binding of VEGF to monomeric VEGFR1D2. We used pBBR plasmid as a backbone and transfered VEGFR1D2 into Escherichia coli Nissle 1917, and finally succeeded in VEGFR1D2-expressing.

Jamboree Program
Figure 2. Predictions of VEGFR1D2 Secondary Structure

Jamboree Program
Figure 3. VEGFR1D2 Trypsin Digestion Analysis(Numbers refer to the human VEGFR1 protein sequence, underlined residues are involved in a disulfide bridge, the proline in bold indicates that the Arg-Pro bond is not cleaved by trypsin22. exp = experimental, calc = calculated.)

Jamboree Program
Figure 4. structure of VEGFR1D2

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 2382
    Illegal XbaI site found at 1296
    Illegal PstI site found at 123
    Illegal PstI site found at 1284
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 2382
    Illegal PstI site found at 123
    Illegal PstI site found at 1284
    Illegal NotI site found at 5314
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 2382
    Illegal BglII site found at 6060
    Illegal BamHI site found at 1302
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 2382
    Illegal XbaI site found at 1296
    Illegal PstI site found at 123
    Illegal PstI site found at 1284
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 2382
    Illegal XbaI site found at 1296
    Illegal PstI site found at 123
    Illegal PstI site found at 1284
    Illegal NgoMIV site found at 574
    Illegal NgoMIV site found at 857
    Illegal NgoMIV site found at 3040
    Illegal AgeI site found at 1955
    Illegal AgeI site found at 2880
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 5636
    Illegal SapI.rc site found at 423
    Illegal SapI.rc site found at 633


[edit]
Categories
//plasmid
Parameters
biologyEscherichia coli Nissle 1917