In vitro panning of a targeting peptide to hepatocarcinoma from a phage display peptide library

Biochem Biophys Res Commun. 2006 Apr 14;342(3):956-62. doi: 10.1016/j.bbrc.2006.02.050.

Abstract

Phage display technology has been used as a powerful tool in the discovery of ligands specific to receptor(s) on the surface of a cancer cell and could also impact clinical issues including functional diagnosis and cell-specific drug delivery. After three rounds of in vitro panning and two rounds of reverse absorption, a group of phages capable of addressing BEL-7402 enormously were obtained for further analysis. Through a cell-based ELISA, immunofluorescence, FACS, and in vivo binding study, WP05 (sequence TACHQHVRMVRP) was demonstrated to be the most effective peptide in targeting four kinds of liver cancer cell lines (BEL-7402, BEL-7404, SMMC-7721, and HepG2), but not the normal liver cell line HL-7702. In conclusion, the peptide WP05 which was screened by in vitro phage display technology was proved to be a targeting peptide to several common hepatocellular carcinoma cell lines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Carcinoma, Hepatocellular / metabolism*
  • Enzyme-Linked Immunosorbent Assay
  • Flow Cytometry
  • Fluorescent Antibody Technique
  • Injections
  • Mice
  • Mice, SCID
  • Molecular Sequence Data
  • Peptide Library*
  • Peptides / metabolism*
  • Protein Binding

Substances

  • Peptide Library
  • Peptides