Mapping protease substrates by using a biotinylated phage substrate library

Chembiochem. 2006 May;7(5):834-8. doi: 10.1002/cbic.200500427.

Abstract

We describe a bacteriophage M13 substrate library encoding the AviTag (BirA substrate) and combinatorial heptamer peptides displayed at the N terminus of the mature form of capsid protein III. Phages are biotinylated efficiently (> or = 50%) when grown in E. coli cells coexpressing BirA, and such viral particles can be immobilized on a streptavidin-coated support and released by protease cleavage within the combinatorial peptide. We have used this library to map the specificity of human Factor Xa and a neuropeptidase, neurolysin (EC3.4.24.16). Validation by analysis of isolated peptide substrates has revealed that neurolysin recognizes the motif hydrophobic-X-Pro-Arg-hydrophobic, where Arg-hydrophobic is the scissile bond.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Bacteriophage M13 / chemistry
  • Biotinylation
  • Factor Xa / chemistry
  • Humans
  • Mass Spectrometry / methods
  • Metalloendopeptidases / chemistry
  • Peptide Hydrolases / chemistry*
  • Peptide Library*
  • Peptides / chemistry
  • Sensitivity and Specificity

Substances

  • Peptide Library
  • Peptides
  • Peptide Hydrolases
  • Factor Xa
  • Metalloendopeptidases
  • neurolysin