The Journal of Antibiotics
Online ISSN : 1881-1469
Print ISSN : 0021-8820
ISSN-L : 0021-8820
MECHANISM OF INHIBITION OF PEPSIN BY PEPSTATIN. II
SETSUKO KUNIMOTOTAKAAKI AOYAGIRINZO NISHIZAWATOMOYOSHI KOMAITOMIO TAKEUCHIHAMAO UMEZAWA
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1974 Volume 27 Issue 6 Pages 413-418

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Abstract

Pepstatin, a strongly bound inhibitor of acid proteases, does not instantaneously bind to pepsin. The dissociation constant of pepsin-pepstatin complex is 9.7 × 10-11 M using Phe•Gly•His•Phe(NO2)•Phe•Ala•PheOMe as substrate. Difference ultraviolet absorption spectra show conformational change of pepsin in interaction with pepstatin. The bindillg of pepsin with pepstatin is stoicheometric and the normality of pepsin can be easily titrated by pepstain. Pepsin modified by 1, 2-epoxy-3-(p-nitrophenoxy) propane, 2, 3-butanedione, α-diazo-p-bromoacetophenone or p-bromophenacyl bromide shows reduced pepstatin-binding activity.

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© Japan Antibiotics Research Association
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