[Development of toxin targeting to VEGF-KDR]

Zhonghua Zhong Liu Za Zhi. 2004 Feb;26(2):78-81.
[Article in Chinese]

Abstract

Objective: To develop toxin targeting vascular endothelial growth factor receptor II (VEGF-II/KDR) fused with a KDR-binling peptide screened from peptide library.

Methods: By affinity to KDR molecular which expressed specifically by new born vascular endothelial cell, peptides to KDR were screened from C7 peptide library by phage display. Among them, a peptide binding to KDR with high affinity termed as P5 was selected and fused to the N-terminal of Shiga toxin subunit A (StxA). The protein (P5-StxA) was expressed in E. coli.

Results: ELISA and Western blot were applied to characterize the binding interaction between the fusion protein, P5-StxA and KDR. Cytotoxicity assay showed that P5-StxA maintained similar toxicity to cell as StxA. In the model of angiogenesis, P5-StxA inhibited selectively VEGF-induced growth of preexisting vessels of the chick chorioallantoic membrane.

Conclusion: These studies demonstrate the small peptide, P5, maybe be used as carrier of toxin targeting to KDR.

Publication types

  • English Abstract

MeSH terms

  • Blotting, Western
  • Enzyme-Linked Immunosorbent Assay
  • Humans
  • Peptide Library
  • Protein Subunits
  • Recombinant Fusion Proteins / metabolism*
  • Shiga Toxin / metabolism*
  • Vascular Endothelial Growth Factor Receptor-2 / metabolism*

Substances

  • Peptide Library
  • Protein Subunits
  • Recombinant Fusion Proteins
  • Shiga Toxin
  • Vascular Endothelial Growth Factor Receptor-2