Characterization of prorenin activation using a synthetic peptide substrate

J Hypertens. 1991 Jun;9(6):483-6. doi: 10.1097/00004872-199106000-00001.

Abstract

Human renin is synthesized as an inactive zymogen (prorenin) which is processed to the active form. We synthesized an 11-amino acid peptide which spans the human prorenin processing site in order to develop a simple assay to study human prorenin activation. Six enzymes which are capable of activating recombinant prorenin in vitro were studied. Four of these enzymes digested the synthetic peptide in a specific fashion, as analyzed by reverse-phase high-performance liquid chromatography. Amino acid analysis of the purified digestion products revealed that trypsin cleaves between Arg-Leu, the authentic processing site, while kallikrein, plasmin and elastase all cleaved at alternate sites. On the other hand, pepsin and cathepsin D did not cleave this substrate, suggesting that the activation of prorenin by these proteases might occur at a site distinct from the authentic processing site. Our data suggest that this synthetic peptide may be used as a simple and specific assay for prorenin activation.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Cathepsin D / metabolism
  • Chromatography, High Pressure Liquid
  • Chromatography, Ion Exchange
  • Enzyme Activation
  • Enzyme Precursors / metabolism*
  • Fibrinolysin / metabolism
  • Humans
  • Kallikreins / metabolism
  • Molecular Sequence Data
  • Pancreatic Elastase / metabolism
  • Pepsin A / metabolism
  • Protein Precursors / chemical synthesis*
  • Renin / chemical synthesis*
  • Renin / metabolism*
  • Substrate Specificity
  • Trypsin / metabolism

Substances

  • Enzyme Precursors
  • Protein Precursors
  • peptide 8A
  • Kallikreins
  • Pancreatic Elastase
  • Trypsin
  • Fibrinolysin
  • Pepsin A
  • Renin
  • Cathepsin D