Generation of Gla-domainless FVIIa by cathepsin G-mediated cleavage

FEBS Lett. 1992 Jul 20;306(2-3):157-60. doi: 10.1016/0014-5793(92)80989-t.

Abstract

Coagulation factor VII contains ten gamma-carboxyglutamic acid residues in the N-terminal region (Gla-domain) which are essential for the hemostatic function of FVII. The present study shows that granulocyte cathepsin G degrades the Gla-domain of FVIIa in vitro. Characterization of the truncated FVIIa by SDS-PAGE and N-terminal amino acid sequence analysis revealed that cleavage had occurred between Tyr-44 and Ser-45 and that further cleavage was only obtained on extensive cathepsin G exposure. Cleavage of vitamin K-dependent coagulation factors by cathepsin G may play a role in vivo, and it offers a convenient way of obtaining proteins deprived of their Gla-domain for functional and structural studies.

MeSH terms

  • 1-Carboxyglutamic Acid / metabolism
  • Amino Acid Sequence
  • Animals
  • Blood Coagulation
  • Cathepsin G
  • Cathepsins / metabolism*
  • Chromatography, High Pressure Liquid
  • Electrophoresis, Polyacrylamide Gel
  • Factor VIIa / chemistry
  • Factor VIIa / metabolism*
  • Humans
  • Isoelectric Focusing
  • Molecular Sequence Data
  • Rabbits
  • Serine Endopeptidases

Substances

  • 1-Carboxyglutamic Acid
  • Cathepsins
  • Serine Endopeptidases
  • CTSG protein, human
  • Cathepsin G
  • Factor VIIa