Heterogeneity and function of mammalian MSRs: enzymes for repair, protection and regulation

被引:79
作者
Hansel, A
Heinemann, SH
Hoshi, T
机构
[1] Univ Penn, Dept Physiol, Philadelphia, PA 19104 USA
[2] Univ Jena, Fac Med, D-07747 Jena, Germany
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2005年 / 1703卷 / 02期
基金
美国国家卫生研究院;
关键词
mammalian methionine sulfoxide reductase; protein oxidation; oxidative stress; MSRA; MSRB; reactive oxygen species;
D O I
10.1016/j.bbapap.2004.09.010
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
Methionine sulfoxide, the physiologically relevant oxidation product of methionine, is enzymatically reduced by peptide methionine sulfoxide reductases (MSRs). Two distinct classes of these enzymes, MSRA and MSRB, which selectively reduce the two methionine sulfoxide epimers, methionine-S-sulfoxide and methionine-R-sulfoxide, respectively, are found in virtually all organisms. Mammals typically possess only one gene encoding MSRA, but at least three genes encoding MSRBs. These MSRs show distinct tissue- and subcellular expression patterns and may play specific functional roles. Susceptibility of some ion channels to reversible methionine oxidation suggests that MSRs have a regulatory role in cellular excitability. Some-if not all-MSRs protect cells and organisms against a variety of oxidative stress episodes, including those by hypoxia and reperfusion, and play a modulatory role in lifespan determination. More MSR-dependent physiological phenomena await to be discovered. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:239 / 247
页数:9
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