Redox Potential and Peroxide Reactivity of Human Peroxiredoxin 3

被引:92
作者
Cox, Andrew G.
Peskin, Alexander V.
Paton, Louise N.
Winterbourn, Christine C.
Hampton, Mark B. [1 ]
机构
[1] Univ Otago, Free Rad Res Grp, Christchurch, New Zealand
关键词
ALPHA-LIPOIC ACID; MITOCHONDRIAL PEROXIREDOXIN-3; THIOREDOXIN REDUCTASE; HYDROGEN-PEROXIDE; OXIDATION; ANTIOXIDANT; CYSTEINE; PEROXYNITRITE; CYCLOPHILIN; EVOLUTION;
D O I
10.1021/bi900558g
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 (Prxs) are a ubiquitous family of thiol peroxidases that protect cells from peroxides and have a putative role in redox. signaling. In this study, we investigated the redox properties of human Prx 3, a typical 2-Cys Prx that is localized to the mitochondrial matrix. We found that Prx 3 displayed strong reactivity with H2O2, with a competitive kinetic approach generating a second order rate constant of 2 x 10(7) M-1 s(-1). This is considerably higher than typical thiols and similar to values for other mammalian 2-Cys Prxs, In contrast, Prx 3 reacted very slowly with the thiol alkylating agents iodoacetamide and N-ethylmaleimide. Using dithiothreitol redox buffers, we measured the redox potential of Prx 3 of -290 mV. This is similar to the redox potential of mitochondrial thioredoxin 2 and is consistent with optimal operation of Prx 3 in the mitochondrial matrix.
引用
收藏
页码:6495 / 6501
页数:7
相关论文
共 40 条
[1]   Redox potentials of glutaredoxins and other thiol-disulfide oxidoreductases of the thioredoxin superfamily determined by direct protein-protein redox equilibria [J].
Åslund, F ;
Berndt, KD ;
Holmgren, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (49) :30780-30786
[2]   Mitochondrial peroxiredoxin 3 is rapidly oxidized in cells treated [J].
Brown, Kristin K. ;
Eriksson, Sofi E. ;
Arner, Elias S. J. ;
Hampton, Mark B. .
FREE RADICAL BIOLOGY AND MEDICINE, 2008, 45 (04) :494-502
[3]  
Cadenas Enrique, 2004, Molecular Aspects of Medicine, V25, P17, DOI 10.1016/j.mam.2004.02.005
[4]   The thioredoxin reductase inhibitor auranofin triggers apoptosis through a Bax/Bak-dependent process that involves peroxiredoxin 3 oxidation [J].
Cox, Andrew G. ;
Brown, Kristin K. ;
Arner, Elias S. J. ;
Hampton, Mark B. .
BIOCHEMICAL PHARMACOLOGY, 2008, 76 (09) :1097-1109
[5]   Oxidation of mitochondrial peroxiredoxin 3 during the initiation of receptor-mediated apoptosis [J].
Cox, Andrew G. ;
Pullar, Juliet M. ;
Hughes, Gillian ;
Ledgerwood, Elizabeth C. ;
Hampton, Mark B. .
FREE RADICAL BIOLOGY AND MEDICINE, 2008, 44 (06) :1001-1009
[6]   Mitochondrial peroxiredoxin 3 is more resilient to hyperoxidation than cytoplasmic peroxiredoxins [J].
Cox, Andrew G. ;
Pearson, Andree G. ;
Pullar, Juliet M. ;
Joensson, Thomas J. ;
Lowther, W. Todd ;
Winterbourn, Christine C. ;
Hampton, Mark B. .
BIOCHEMICAL JOURNAL, 2009, 421 :51-58
[7]   Silencing of peroxiredoxin 3 and peroxiredoxin 5 reveals the role of mitochondrial peroxiredoxins in the protection of human neuroblastoma SH-SY5Y cells toward MPP+ [J].
De Simoni, Stephanie ;
Goemaere, Julie ;
Knoops, Bernard .
NEUROSCIENCE LETTERS, 2008, 433 (03) :219-224
[8]  
Dietz Karl-Josef, 2007, V44, P267
[9]  
Dunford H.B., 1999, Heme Peroxidases
[10]   Redox compartmentalization in eukaryotic cells [J].
Go, Young-Mi ;
Jones, Dean P. .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2008, 1780 (11) :1271-1290