4.5 Article

Human peroxiredoxin 5 is a peroxynitrite reductase

Journal

FEBS LETTERS
Volume 571, Issue 1-3, Pages 161-165

Publisher

WILEY
DOI: 10.1016/j.febslet.2004.06.080

Keywords

peroxiredoxin; peroxynitrite; nitrooxidative stress; mitochondrion; peroxisome; cytosol; nucleus

Ask authors/readers for more resources

Peroxiredoxins are an ubiquitous family of peroxidases widely distributed among prokaryotes and eukaryotes. Peroxiredoxin 5, which is the last discovered mammalian member, was previously shown to reduce peroxides with the use of reducing equivalents derived from thioredoxin. We report here that human peroxiredoxin 5 is also a peroxynitrite reductase. Analysis of peroxiredoxin 5 mutants, in which each of the cysteine residues was mutated, suggests that the nucleophilic attack on the O-O bond of peroxynitrite is performed by the N-terminal peroxidatic Cys(47). Moreover, with the use of pulse radiolysis, we show that human peroxiredoxin 5 reduces peroxynitrite with an unequalled high rate constant of (7 +/- 3) x 10(7) M-1 s(-1). (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available