In vivo parameters influencing 2-Cys Prx oligomerization: The role of enzyme sulfinylation

Redox Biol. 2015 Dec:6:326-333. doi: 10.1016/j.redox.2015.08.011. Epub 2015 Aug 20.

Abstract

2-Cys Prxs are H2O2-specific antioxidants that become inactivated by enzyme hyperoxidation at elevated H2O2 levels. Although hyperoxidation restricts the antioxidant physiological role of these enzymes, it also allows the enzyme to become an efficient chaperone holdase. The critical molecular event allowing the peroxidase to chaperone switch is thought to be the enzyme assembly into high molecular weight (HMW) structures brought about by enzyme hyperoxidation. How hyperoxidation promotes HMW assembly is not well understood and Prx mutants allowing disentangling its peroxidase and chaperone functions are lacking. To begin addressing the link between enzyme hyperoxidation and HMW structures formation, we have evaluated the in vivo 2-Cys Prxs quaternary structure changes induced by H2O2 by size exclusion chromatography (SEC) on crude lysates, using wild type (Wt) untagged and Myc-tagged S. cerevisiae 2-Cys Prx Tsa1 and derivative Tsa1 mutants or genetic conditions known to inactivate peroxidase or chaperone activity or altering the enzyme sensitivity to hyperoxidation. Our data confirm the strict causative link between H2O2-induced hyperoxidation and HMW formation/stabilization, also raising the question of whether CP hyperoxidation triggers the assembly of HMW structures by the stacking of decamers, which is the prevalent view of the literature, or rather, the stabilization of preassembled stacked decamers.

Keywords: Chaperone; H(2)O(2); Peroxidase; Peroxiredoxin; S. cerevisiae; Sulfiredoxin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatography, Gel
  • Gene Expression Regulation, Fungal*
  • Hydrogen Peroxide / pharmacology
  • Isoenzymes / chemistry
  • Isoenzymes / genetics
  • Isoenzymes / metabolism
  • Molecular Chaperones / chemistry*
  • Molecular Chaperones / genetics
  • Molecular Chaperones / metabolism
  • Mutation
  • Peroxidases / chemistry*
  • Peroxidases / genetics
  • Peroxidases / metabolism
  • Plasmids / chemistry
  • Plasmids / metabolism
  • Protein Multimerization
  • Protein Structure, Quaternary
  • Recombinant Fusion Proteins / chemistry*
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Saccharomyces cerevisiae / drug effects
  • Saccharomyces cerevisiae / enzymology
  • Saccharomyces cerevisiae / genetics*
  • Saccharomyces cerevisiae Proteins / chemistry*
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism
  • Sulfinic Acids / chemistry*
  • Sulfinic Acids / metabolism

Substances

  • Isoenzymes
  • Molecular Chaperones
  • Recombinant Fusion Proteins
  • Saccharomyces cerevisiae Proteins
  • Sulfinic Acids
  • Hydrogen Peroxide
  • Peroxidases
  • Tsa1 protein, S cerevisiae