Literature DB >> 9860480

Kinetic study of the reaction of glutathione peroxidase with peroxynitrite.

K Briviba1, R Kissner, W H Koppenol, H Sies.   

Abstract

Glutathione peroxidases and their mimics, e.g., ebselen or diaryl tellurides, efficiently reduce peroxynitrite/peroxynitrous acid (ONOO-/ONOOH) to nitrite and protect against oxidation and nitration reactions. Here, we report the second-order rate constant for the reaction of the reduced form of glutathione peroxidase (GPx) with peroxynitrite as (8.0 +/- 0.8) x 10(6) M-1 s-1 (per GPx tetramer) at pH 7.4 and 25 degreesC. The rate constant for oxidized GPx is about 10 times lower, (0.7 +/- 0.2) x 10(6) M-1 s-1. On a selenium basis, the rate constant for reduced GPx is similar to that obtained previously for ebselen. The data support the conclusion that GPx can exhibit a biological function by acting as a peroxynitrite reductase.

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Year:  1998        PMID: 9860480     DOI: 10.1021/tx980086y

Source DB:  PubMed          Journal:  Chem Res Toxicol        ISSN: 0893-228X            Impact factor:   3.739


  17 in total

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Authors:  G R Martinez; P Di Mascio; M G Bonini; O Augusto; K Briviba; H Sies; P Maurer; U Röthlisberger; S Herold; W H Koppenol
Journal:  Proc Natl Acad Sci U S A       Date:  2000-09-12       Impact factor: 11.205

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