Literature DB >> 12853451

Regeneration of peroxiredoxins during recovery after oxidative stress: only some overoxidized peroxiredoxins can be reduced during recovery after oxidative stress.

Mireille Chevallet1, Elsa Wagner, Sylvie Luche, Alain van Dorsselaer, Emmanuelle Leize-Wagner, Thierry Rabilloud.   

Abstract

Peroxiredoxins (prx) are redox enzymes using an activated cysteine as their active site. This activated cysteine can be easily overoxidized to cysteine sulfinic acid or cysteine sulfonic acid, especially under oxidative stress conditions. The regeneration of peroxiredoxins after a short, intense oxidative stress was studied, using a proteomics approach. Important differences in regeneration speed were found, prx2 being the fastest regenerated protein, followed by prx1, whereas prx3 and prx6 were regenerated very slowly. Further study of the mechanism of this regeneration by pulse-chase experiments using stable isotope labeling and cycloheximide demonstrated that the fast-regenerating peroxiredoxins are regenerated at least in part by a retroreduction mechanism. This demonstrates that the overoxidation can be reversible under certain conditions. The pathway of this retroreduction and the reasons explaining the various regeneration speeds of the peroxiredoxins remain to be elucidated.

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Year:  2003        PMID: 12853451     DOI: 10.1074/jbc.M305161200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  48 in total

1.  The Parkinson's disease protein DJ-1 is neuroprotective due to cysteine-sulfinic acid-driven mitochondrial localization.

Authors:  Rosa M Canet-Avilés; Mark A Wilson; David W Miller; Rili Ahmad; Chris McLendon; Sourav Bandyopadhyay; Melisa J Baptista; Dagmar Ringe; Gregory A Petsko; Mark R Cookson
Journal:  Proc Natl Acad Sci U S A       Date:  2004-06-04       Impact factor: 11.205

2.  ProMoST (Protein Modification Screening Tool): a web-based tool for mapping protein modifications on two-dimensional gels.

Authors:  Brian D Halligan; Victor Ruotti; Weihong Jin; Scott Laffoon; Simon N Twigger; Edward A Dratz
Journal:  Nucleic Acids Res       Date:  2004-07-01       Impact factor: 16.971

Review 3.  The peroxiredoxin repair proteins.

Authors:  Thomas J Jönsson; W Todd Lowther
Journal:  Subcell Biochem       Date:  2007

4.  Peroxiredoxin II expression and its association with oxidative stress and cell proliferation in human idiopathic pulmonary fibrosis.

Authors:  Kirsi Vuorinen; Steffen Ohlmeier; Outi Leppäranta; Kaisa Salmenkivi; Marjukka Myllärniemi; Vuokko L Kinnula
Journal:  J Histochem Cytochem       Date:  2008-07-07       Impact factor: 2.479

5.  Sulfiredoxin Translocation into Mitochondria Plays a Crucial Role in Reducing Hyperoxidized Peroxiredoxin III.

Authors:  You Hyun Noh; Jin Young Baek; Woojin Jeong; Sue Goo Rhee; Tong-Shin Chang
Journal:  J Biol Chem       Date:  2009-01-28       Impact factor: 5.157

6.  Peroxidatic cysteine residue of peroxiredoxin 2 separated from human red blood cells treated by tert-butyl hydroperoxide is hyperoxidized into sulfinic and sulfonic acids.

Authors:  Yo-Ichi Ishida; Mariko Aki; Sohta Fujiwara; Masami Nagahama; Yuki Ogasawara
Journal:  Hum Cell       Date:  2017-04-22       Impact factor: 4.174

Review 7.  Signaling functions of reactive oxygen species.

Authors:  Henry Jay Forman; Matilde Maiorino; Fulvio Ursini
Journal:  Biochemistry       Date:  2010-02-09       Impact factor: 3.162

8.  Kinetic analysis of structural influences on the susceptibility of peroxiredoxins 2 and 3 to hyperoxidation.

Authors:  Rebecca A Poynton; Alexander V Peskin; Alexina C Haynes; W Todd Lowther; Mark B Hampton; Christine C Winterbourn
Journal:  Biochem J       Date:  2015-11-27       Impact factor: 3.857

9.  Hyperhomocysteinemia during aortic aneurysm, a plausible role of epigenetics.

Authors:  Nithya Narayanan; Neetu Tyagi; Amy Shah; Sebastian Pagni; Suresh C Tyagi
Journal:  Int J Physiol Pathophysiol Pharmacol       Date:  2013-03-08

10.  Characterization of plant sulfiredoxin and role of sulphinic form of 2-Cys peroxiredoxin.

Authors:  Iván Iglesias-Baena; Sergio Barranco-Medina; Alfonso Lázaro-Payo; Francisco Javier López-Jaramillo; Francisca Sevilla; Juan-José Lázaro
Journal:  J Exp Bot       Date:  2010-02-22       Impact factor: 6.992

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