Peroxiredoxin Evolution and the Regulation of Hydrogen Peroxide Signaling

Author:

Wood Zachary A.12,Poole Leslie B.12,Karplus P. Andrew12

Affiliation:

1. Department of Biochemistry and Biophysics, Oregon State University, Corvallis, OR 97333, USA.

2. Department of Biochemistry, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.

Abstract

Eukaryotic 2-Cys peroxiredoxins (2-Cys Prxs) not only act as antioxidants, but also appear to regulate hydrogen peroxide–mediated signal transduction. We showthat bacterial 2-Cys Prxs are much less sensitive to oxidative inactivation than are eukaryotic 2-Cys Prxs. By identifying two sequence motifs unique to the sensitive 2-Cys Prxs and comparing the crystal structure of a bacterial 2-Cys Prx at 2.2 angstrom resolution with other Prx structures, we define the structural origins of sensitivity. We suggest this adaptation allows 2-Cys Prxs to act as floodgates, keeping resting levels of hydrogen peroxide low, while permitting higher levels during signal transduction.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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