Isolation and characterization of an anticoagulant proteinase, cerastase F-4, from Cerastes cerastes (Egyptian sand viper) venom

Thromb Res. 1986 Apr 1;42(1):55-62. doi: 10.1016/0049-3848(86)90196-9.

Abstract

An anticoagulant protease, Cerastase F-4, was isolated from the venom of Cerastes cerastes (Egyptian sand viper) by a combination of gel filtration, ion-exchange chromatography, and HPLC. Homogeneity of the purified anticoagulant was established by discontinuous polyacrylamide disc gel electrophoresis and by isotachophoresis. The anticoagulant enzyme is a single polypeptide chain without subunits having a molecular weight of 22,500. It consists of 28% aspartic acid residues and only 7% are basic amino acids. This agrees well with the fact that the anticoagulant is an acidic protein with an isoelectric point of 5.2. The anticoagulant is a proteolytic enzyme which hydrolyzes casein, fibrinogen and fibrin. The enzyme's optimum activity occurs around 55 degrees C. The anticoagulant showed no phospholipase A activity, low lethal activity, low hemorrhagic and capillary permeability activity, and no myotoxic activity.

Publication types

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

MeSH terms

  • Amino Acids / analysis
  • Animals
  • Anticoagulants / isolation & purification*
  • Chromatography, Gel
  • Chromatography, High Pressure Liquid
  • Chromatography, Ion Exchange
  • Endopeptidases / isolation & purification*
  • Endopeptidases / pharmacology
  • Fibrinogen / metabolism
  • Fibrinolysis / drug effects
  • Hemolysis / drug effects
  • Isoelectric Point
  • Molecular Weight
  • Substrate Specificity
  • Viper Venoms / analysis*

Substances

  • Amino Acids
  • Anticoagulants
  • Viper Venoms
  • Fibrinogen
  • Endopeptidases
  • cerastase F-4