A cyclopeptidic suicide substrate preferentially inactivates urokinase-type plasminogen activator

Biochem Biophys Res Commun. 1991 Jul 15;178(1):352-9. doi: 10.1016/0006-291x(91)91821-s.

Abstract

c[Arg-aB-(CH2+SCH3 phi)-Gly4] was designed and studied as a mechanism-based inactivator (suicide substrate) for plasminogen activators (u-PA and t-PA) and plasmin. This compound inhibited u-PA and fulfills criteria expected for the involvement of an enzyme-activated inhibitor: first-order and irreversible process, saturation kinetics, protection by substrate. The limiting first-order rate constant kinact and the apparent enzyme-inhibitor dissociation constant KI were 0.021 s-1 and 9 microM, respectively at pH 7.5 and 25 degrees C. The activation of plasminogen by u-PA is compromised after this enzyme has been treated by the reagent. Plasmin and t-PA were inactivated 40- and 2330-fold less efficiently than u-PA, respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Binding Sites
  • Enzyme Precursors / antagonists & inhibitors
  • Fibrinolysin / antagonists & inhibitors
  • Humans
  • Kinetics
  • Molecular Sequence Data
  • Peptides, Cyclic / pharmacology*
  • Plasminogen Activators / antagonists & inhibitors*
  • Plasminogen Activators / urine
  • Plasminogen Inactivators*
  • Tissue Plasminogen Activator / antagonists & inhibitors
  • Urokinase-Type Plasminogen Activator / antagonists & inhibitors*
  • Urokinase-Type Plasminogen Activator / urine

Substances

  • Enzyme Precursors
  • Peptides, Cyclic
  • Plasminogen Inactivators
  • Plasminogen Activators
  • Tissue Plasminogen Activator
  • Fibrinolysin
  • Urokinase-Type Plasminogen Activator