Developing peptide inhibitors to thrombin activation of platelets from bradykinin analogs

Thromb Res. 2001 Dec 15;104(6):451-65. doi: 10.1016/s0049-3848(01)00387-5.

Abstract

Investigations identified peptide, platelet-selective thrombin inhibitors. Three peptides (MAP4-RPPGF, RGKWC and RGDWC) were relatively selective inhibitors of thrombin-induced platelet activation and calcium mobilization. MAP4-RPPGF at 35.5+/-0.03 microM inhibits gamma-thrombin-induced platelet aggregation 100% and alpha-thrombin-induced calcium mobilization in fibroblasts 84%. RGKWC at 800+/-400 microM inhibits gamma-thrombin-induced platelet aggregation 100% and calcium mobilization 63%. RGDWC at 140+/-100 microM inhibits gamma-thrombin-induced platelet aggregation 100% and calcium mobilization 32%. RGDWC also inhibits ADP-induced platelet aggregation, whereas MAP4-RPPGF and RGKWC do not. RGKWC prolongs the activated partial thromboplastin time (APTT) but not the prothrombin time (PT) or thrombin clotting time (TCT). RGKWC uniquely inhibits alpha-thrombin activation of human factor XI. Single amino acid substitutions in peptide pentamers result in differences in potency and mechanism(s) of inhibition of platelet and fibroblast activation by thrombin.

Publication types

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

MeSH terms

  • Adenosine Diphosphate / pharmacology
  • Amino Acid Sequence
  • Blood Coagulation Tests
  • Bradykinin / analogs & derivatives*
  • Bradykinin / chemical synthesis
  • Bradykinin / pharmacology
  • Calcium Signaling / drug effects
  • Combinatorial Chemistry Techniques
  • Dose-Response Relationship, Drug
  • Drug Design*
  • Humans
  • Oligopeptides / chemical synthesis
  • Oligopeptides / pharmacology*
  • Peptide Library
  • Platelet Activation / drug effects*
  • Structure-Activity Relationship
  • Thrombin / antagonists & inhibitors*
  • Thrombin / pharmacology
  • Thrombin / physiology

Substances

  • Oligopeptides
  • Peptide Library
  • Adenosine Diphosphate
  • Thrombin
  • Bradykinin