Simulation oligopeptide of vascular endothelial growth factor (VEGF) epitope and application of simulation oligopeptide
A growth factor and vascular endothelial technology, applied in the field of vascular endothelial cell growth factor VEGF antigen, can solve the problems that limit the wide application of polypeptide drugs, achieve obvious anti-angiogenesis effect, obvious anti-tumor effect, and easy synthesis and construction
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Embodiment 1
[0023] Through the method of phage display, the analog short peptide CPU-510-02 of endothelial cell growth factor VEGF epitope was obtained:
[0024] (1) Obtain the nucleotide sequence of the analog short peptide CPU-510-02 of endothelial cell growth factor VEGF antigen epitope through the screening of phage random peptide library:
[0025] A. Biopanning of phage random 7-peptide library: Anti-VEGF monoclonal antibody was coated with coating solution (0.1M NaHCO 3 , pH8.6) was diluted to 100 μg / ml, and 150 μl of the solution was used to coat one well of the microtiter plate, overnight at 4°C. Aspirate the coating solution, add blocking solution (0.1M NaHCO 3, pH8.6, 5mg / ml BSA), at 4°C for at least one hour. Aspirate the blocking solution and wash 6 times with 0.1% TBST [TBS+0.1% (v / v) Tween-20]. Dilute 10 μl of the original phage polypeptide library with 100 μl TBST, then add it to the wells coated with anti-VEGF monoclonal antibody, react at room temperature for 1 hour, p...
Embodiment 2
[0033] Proliferation inhibitory test of peptides on human umbilical vein endothelial cells HUVEC, melanoma cells B16F10, gastric cancer cells SGC7901 and liver cancer cells HepG2:
[0034] (1) MTT method to measure the inhibitory effect of epitope peptides on HUVEC proliferation in the presence of VEGF: take human umbilical vein endothelial cells in logarithmic growth phase HUVEC, digest with an appropriate amount of 0.25% trypsin solution, and shake gently to make the digestive juice evenly act For the cells, remove the digestive juice when the sheets of cells are round and shrunk to a single cell state, quickly add an appropriate amount of medium, and blow gently with a pipette to form a single-cell suspension; take the single-cell suspension and count it as 5000 cells per well Inoculated in a 96-well plate (edge wells were filled with sterile PBS), with DMEM containing 10% calf serum at 37 ° C, containing 5% CO 2 Cultured in a constant temperature incubator for 24 hours t...
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