Screening peptides binding specifically to large intestinal cancer LoVo cells from phage random peptide library.
- Author:
Kang-Xiong LIAO
1
;
Xue-Qing YAO
;
Cheng-Tang WU
;
Feng LIN
;
Wu-Lin WU
;
Sui-de ZENG
;
Yu-Qi LUO
;
Shang-Tong LEI
Author Information
- Publication Type:Journal Article
- MeSH: Amino Acid Sequence; Base Sequence; Binding, Competitive; Cell Line, Tumor; Colorectal Neoplasms; genetics; metabolism; pathology; Humans; Molecular Sequence Data; Peptide Library; Peptides; genetics; isolation & purification; metabolism; Protein Binding
- From: Journal of Southern Medical University 2008;28(6):986-990
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo screen the polypeptides specifically binding to human large intestinal cancer LoVo cells from a phage-displayed peptide library for potential use as targeting vectors for large intestinal cancer therapy.
METHODSWith the LoVo cells as the target cells and human normal large intestinal mucosal epithelial cells as the absorber cells for subtraction biopanning from a c7c phage-display peptide library, the positive phage clones were identified by enzyme-linked immunosorbent assay (ELISA) and immunofluorescence detection. The amino acid sequences of the identified peptides were deduced by DNA sequencing.
RESULTSAfter 3 rounds of screening, 5 positive phage clones showing specific binding to LoVo cells and containing conserved motif RPMP were obtained from the 20 randomly selected clones.
CONCLUSIONSpecific peptide against large intestinal cancer cells can be obtained from a phage-display peptide library for use as potential vectors for targeting therapy of large intestinal cancer.