Glutaredoxin s12: unique properties for redox signaling

Antioxid Redox Signal. 2012 Jan 1;16(1):17-32. doi: 10.1089/ars.2011.3933. Epub 2011 Aug 30.

Abstract

Aims: Cysteines (Cys) made acidic by the protein environment are generally sensitive to pro-oxidant molecules. Glutathionylation is a post-translational modification that can occur by spontaneous reaction of reduced glutathione (GSH) with oxidized Cys as sulfenic acids (-SOH). The reverse reaction (deglutathionylation) is strongly stimulated by glutaredoxins (Grx) and requires a reductant, often GSH.

Results: Here, we show that chloroplast GrxS12 from poplar efficiently reacts with glutathionylated substrates in a GSH-dependent ping pong mechanism. The pK(a) of GrxS12 catalytic Cys is very low (3.9) and makes GrxS12 itself sensitive to oxidation by H(2)O(2) and to direct glutathionylation by nitrosoglutathione. Glutathionylated-GrxS12 (GrxS12-SSG) is temporarily inactive until it is deglutathionylated by GSH. The equilibrium between GrxS12 and glutathione (E(m(GrxS12-SSG))= -315 mV, pH 7.0) is characterized by K(ox) values of 310 at pH 7.0, as in darkened chloroplasts, and 69 at pH 7.9, as in illuminated chloroplasts.

Innovation: Based on thermodynamic data, GrxS12-SSG is predicted to accumulate in vivo under conditions of mild oxidation of the GSH pool that may occur under stress. Moreover, GrxS12-SSG is predicted to be more stable in chloroplasts in the dark than in the light.

Conclusion: These peculiar catalytic and thermodynamic properties could allow GrxS12 to act as a stress-related redox sensor, thus allowing glutathione to play a signaling role through glutathionylation of GrxS12 target proteins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkylation
  • Amino Acid Substitution
  • Catalysis
  • Catalytic Domain
  • Enzyme Activation / drug effects
  • Enzyme Inhibitors / pharmacology
  • Glutaredoxins / antagonists & inhibitors
  • Glutaredoxins / genetics
  • Glutaredoxins / metabolism*
  • Hydrogen-Ion Concentration
  • Iodoacetamide / pharmacology
  • Kinetics
  • Oxidation-Reduction
  • Populus / enzymology
  • Signal Transduction*
  • Substrate Specificity

Substances

  • Enzyme Inhibitors
  • Glutaredoxins
  • Iodoacetamide