Distinct mechanisms contribute to stringent substrate specificity of tissue-type plasminogen activator

J Biol Chem. 1996 Feb 23;271(8):4461-7. doi: 10.1074/jbc.271.8.4461.

Abstract

Tissue-type plasminogen activator (t-PA) has evolved to optimize cleavage of plasminogen (Plg) while minimizing cleavage of other potential protein and peptide substrates. We find that the S2 and S2 subsites of t-PA are important determinants of specificity, and occupancy of the S3 subsite is essential for catalysis. t-PA efficiently hydrolyzes a protein substrate which incorporates an optimized substrate sequence, revealing the ability of the protease to participate in the highly selective cleavage of protein fusions. Surprisingly, t-PA cleaves this engineered protein substrate with a Km that is reduced 950-fold relative to the Km for hydrolysis of the same target sequence within a peptide. This reduction of Km suggests that binding is facilitated by interactions between protein substrate and protease that are distant from the P4-P2' residues. We use this kinetic data to derive a model in which several distinct mechanisms contribute to the remarkable specificity of t-PA.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Catalysis
  • Cattle
  • Kinetics
  • Molecular Sequence Data
  • Ornithine Decarboxylase / metabolism
  • Peptides / chemical synthesis
  • Peptides / metabolism
  • Plasminogen / metabolism
  • Recombinant Proteins / metabolism
  • Substrate Specificity
  • Tissue Plasminogen Activator / metabolism*
  • Trypsin / metabolism

Substances

  • Peptides
  • Recombinant Proteins
  • Plasminogen
  • Trypsin
  • Tissue Plasminogen Activator
  • Ornithine Decarboxylase