1. Academic Validation
  2. Affinity purification of endothia protease with a novel renin inhibitor SQ 32,970

Affinity purification of endothia protease with a novel renin inhibitor SQ 32,970

  • Biochem Biophys Res Commun. 1989 May 30;161(1):1-7. doi: 10.1016/0006-291x(89)91551-9.
J A Norman 1 D Little C A Free T Dejneka H Weber D E Ryono
Affiliations

Affiliation

  • 1 Department of Pharmacology, Squibb Institute for Medical Research, Princeton, New Jersey.
Abstract

A novel tripeptidic Renin Inhibitor is described, SQ 32,970, that will potently inhibit endothia protease. This inhibitor can be coupled to Sepharose and will allow the affinity-purification of endothia protease in one step to greater than 95% purity as measured by SDS PAGE. The purified endothia protease cleaves the Lys-Pro-Ala-Glu-Phe-Nph-Arg-Leu substrate at the Phe-Nph bond with a Kcat/Km of 7445 (s-1 mM-1) at pH 3.1 and 4057 (s-1 mM-1) at pH 6.0. Affinity purified endothia protease can be crystallized in the pH range in which it is enzymatically active and can be inhibited by Renin inhibitors.

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