Mimic short peptide 7B of endothelial cell growth factor VEGF antigen epitope and application thereof

Abstract

The invention discloses a mimic short peptide 7B of endothelial cell growth factor VEGF antigen epitope and an application thereof. The amino acid sequence of the mimic short peptide 7B is FKPSCVPLMRCGGCCN and the nucleotide sequence is TTCAAACCGTCCTGCGTTCCGCTGATGCGTTGCGGTGGTTGTGCAACG. In vitro experiments show that the mimic short peptide 7B of the invention has obvious inhibiting effect during the processes of endothelial cell proliferation and tube formation and the tumor cell proliferation and migration. Therefore, the mimic short peptide 7B of the invention can be used for preparing peptide vaccines, tumor angiogenesis inhibitor or tumor-oriented drugs, and has great reference value on diagnosing and predicting tumorigenesis by utilizing VEGF receptor as a target, discussing development of small molecular peptides on the tumor angiogenesis inhibitors, and developing and researching tumor-oriented drugs.

Description

technical field [0001] The invention belongs to the fields of molecular biology and medicine, and particularly relates to a short analog peptide 7B of endothelial cell growth factor VEGF antigen epitope and application thereof. Background technique [0002] VEGF is a homodimeric protein with a relative molecular weight of 34-42KD that was first purified by Ferrara in the in vitro culture medium of bovine pituitary follicular astrocytes in 1989. The human VEGF gene structure is located on chromosome 6p21.3, consisting of 8 exons and 7 introns alternately. According to the splicing mode of its mRNA, five different VEGF isoforms are produced, including VEGF206, VEGF189, VEGF165, VEGF145 and VEGF121. These 5 isomers of VEGF all have the activity of inducing endothelial cell proliferation and are effective angiogenesis and permeability inducing factors. The difference mainly lies in their affinity with heparin on the cell surface and in the extracellular matrix. [0003] VEGF a...

AI Technical Summary

Problems solved by technology

[0006] Among the current peptide drugs, in terms of anti-tumor, Kathleen et al. synthesized two peptides through artificial chemistry. The results showed that the peptide had a high inhibitory rate on human cervical cancer cells, but the peptide had no significant effect on human VEGF. Homology, and the conserved motif MXXP with anti-tumor activity obtained by Maruta et al. has no homology with FGFs

The artificial synthesis of these peptides is expensive, and if used as a vaccine, it may induce the production of antibodies specific to the peptide in the human body, thereby preventing its anti-tumor effect from being exerted

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