A novel method for selection of chymotrypsin inhibitors from a phage peptide library

Biochem Mol Biol Int. 1998 Jun;45(1):155-61. doi: 10.1080/15216549800202522.

Abstract

A novel screening strategy has been developed for the identification of alpha-chymotrypsin inhibitors from a phage peptide library. In this strategy, the standard affinity selection protocol was modified by adding a proteolytic cleavage period to avoid recovery of alpha-chymotrypsin substrates. After four cycles of selection and further activity assay, a group of related peptides were identified by DNA sequencing. These peptides share a consensus sequence motif as (S/T)RVPR(R/H). Then, a corresponding short peptide (Ac-ASRVPRRG-NH2) was synthesized chemically and proved to be an inhibitor of alpha-chymotrypsin. The present work provides a useful way for searching proteinase inhibitors without detailed knowledge of the molecular structure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacteriophages / metabolism*
  • Chymotrypsin / antagonists & inhibitors*
  • Enzyme Activation / drug effects
  • Escherichia coli / virology
  • Hydrolysis
  • Oligopeptides / chemical synthesis
  • Oligopeptides / metabolism
  • Peptide Library*
  • Protein Binding / drug effects
  • Protein Engineering / methods
  • Serine Proteinase Inhibitors / metabolism
  • Serine Proteinase Inhibitors / pharmacology*

Substances

  • Oligopeptides
  • Peptide Library
  • Serine Proteinase Inhibitors
  • Chymotrypsin