Human peroxiredoxin 5 is a peroxynitrite reductase

被引:156
作者
Dubuisson, M
Stricht, DV
Clippe, A
Etienne, F
Nauser, T
Kissner, R
Koppenol, WH
Rees, JF
Knoops, B [1 ]
机构
[1] Catholic Univ Louvain, Inst Sci Vie, Cell Biol Lab, B-1348 Louvain, Belgium
[2] ETH Honggerberg, Anorgan Chem Lab, CH-8093 Zurich, Switzerland
基金
澳大利亚研究理事会;
关键词
peroxiredoxin; peroxynitrite; nitrooxidative stress; mitochondrion; peroxisome; cytosol; nucleus;
D O I
10.1016/j.febslet.2004.06.080
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:161 / 165
页数:5
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