A comparison between activated protein C and des-1-41-light chain-activated protein C in reactions with type 1 plasminogen activator inhibitor

Blood. 1989 Jul;74(1):173-81.

Abstract

This study investigates the role of the gamma-carboxyglutamic acid (gla) containing domain of activated protein C in interactions with both platelet-derived and purified type 1 plasminogen activator inhibitor (PAI-1). The activity of human platelet PAI-1 was neutralized to the same extent by bovine activated protein C and bovine des-1-41-light chain-activated protein C. Both forms of activated protein C formed SDS-stable, divalent-cation independent complexes with platelet PAI-1, as demonstrated by immunoblotting using antibodies directed to either protein C or PAI-1. Since activated protein C neutralized PAI-1, the potential inhibition of the enzyme by PAI-1 was studied. Purified PAI-1 inhibited the amidolytic activity of bovine-activated protein C and bovine des-1-41-light chain-activated protein C with a k2 of 2.85 X 10(4) M-1 sec-1 for both proteins. These data suggest that the gla domain of activated protein C is not required for neutralization of PAI-1 activity, for complex formation with PAI-1, or for inhibition of the amidolytic activity of activated protein C by PAI-1.

Publication types

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

MeSH terms

  • Animals
  • Blood Platelets / enzymology*
  • Blotting, Western
  • Cattle
  • Enzyme Activation
  • Glycoproteins / metabolism*
  • Humans
  • In Vitro Techniques
  • Macromolecular Substances
  • Molecular Weight
  • Plasminogen Inactivators
  • Protease Inhibitors / metabolism
  • Protein Binding
  • Protein C / antagonists & inhibitors
  • Protein C / metabolism*
  • Structure-Activity Relationship

Substances

  • Glycoproteins
  • Macromolecular Substances
  • Plasminogen Inactivators
  • Protease Inhibitors
  • Protein C