Design and synthesis of thrombin substrates with modified kinetic parameters

Dirk S. Rijkers, Simone J. H. Wielders, Godefridus I. Tesser, H. Coenraad Hemker

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

For the continuous registration of thrombin formation in plasma (1), selective thrombin substrates are required, that show moderate binding affinities (high K(m)) and low turnover numbers (low k(cat)). Previously we have used SQ68 (CH3O-CO-CH2-CO-Aib-Arg-pNA) for this purpose. In order to find more substrates suitable for this application, we synthesized a series of 25 peptide p-nitroanilides. As lead structures SQ68 and S2238 (H-D-Phe-Pip-Arg-pNA) were used. By introduction of specific structure modifications we tried to alter the kinetic data in the required direction. The modifications were designed on basis of existing knowledge on the structure of the thrombin active-site and its surroundings. We indeed obtained a number of substrates with the kinetic constants in the desired range.
Original languageEnglish
Pages (from-to)491-499
Number of pages9
JournalThrombosis Research
Volume79
Issue number5-6
DOIs
Publication statusPublished - 18 Feb 1995
Externally publishedYes

Keywords

  • Chemical synthesis
  • Chromogenic substrates
  • Thrombin substrates
  • chromogenic substrate
  • dextro phenylalanylpipecolylarginine 4 nitroanilide
  • peptide
  • sq68
  • thrombin
  • unclassified drug
  • article
  • blood clotting
  • controlled study
  • human
  • priority journal

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