Characterization of Ac1-Proteinase from the venom of Agkistrodon acutus (Hundred-pace snake) from Taiwan

Int J Biochem. 1991;23(3):311-5. doi: 10.1016/0020-711x(91)90112-z.

Abstract

1. Ac1-Proteinase from the venom of Agkistrodon acutus was isolated in a homogeneous form by a previously published method. 2. Ac1-Proteinase possessed lethal, hemorrhagic, caseinolytic, azocaseinolytic, azoalbumin hydrolytic and hide powder azure hydrolytic activities. 3. The toxin also hydrolyzed the oxidized B chain of insulin and fibrinogen. The cleavage sites in the oxidized B chain of insulin were identified as Ala(14)-Leu(15) and Tyr(16)-Leu(17). The A alpha chain of fibrinogen was digested. 4. Biological properties of Ac1-Proteinase were investigated further and are reported in this paper.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Crotalid Venoms / analysis*
  • Endopeptidases / isolation & purification
  • Endopeptidases / metabolism*
  • Endopeptidases / toxicity
  • Fibrinogen / metabolism
  • Hemorrhage / chemically induced
  • Hydrolysis
  • Insulin / metabolism
  • Mice
  • Mice, Inbred ICR
  • Molecular Sequence Data
  • Muscles / pathology
  • Muscular Diseases / chemically induced
  • Necrosis / chemically induced
  • Peptide Fragments / metabolism
  • Substrate Specificity

Substances

  • Agkistrodon venoms
  • Crotalid Venoms
  • Insulin
  • Peptide Fragments
  • Fibrinogen
  • Endopeptidases
  • Ac1-proteinase