How much H(2)O(2) is produced by recombinant D-amino acid oxidase in mammalian cells?

Antioxid Redox Signal. 2014 Mar 1;20(7):1039-44. doi: 10.1089/ars.2013.5618. Epub 2013 Oct 23.

Abstract

Yeast D-amino acid oxidase (DAO) can serve as a genetically encoded producer of reactive oxygen species (ROS) in redox signaling studies. However, dynamics of hydrogen peroxide production and its sensitivity to externally added D-alanine (D-Ala) in cells have not been determined. Here we show that DAO, fused to a genetically encoded H2O2 indicator HyPer, can be used for controlled production of ROS in living eukaryotic cells. We found a clear heterogeneity in ROS production dynamics between individual cells. Moreover, different cell lines demonstrated distinct sensitivity to added D-Ala. Finally, by comparing signals generated by the HyPer-DAO fusion protein versus coexpressed HyPer and DAO proteins, we show that the fusion system is more sensitive to hydrogen peroxide production. Our results show the utility of the HyPer-DAO genetically encoded system for redox signaling studies and suggest that H2O2 produced by DAO in the cytoplasm acts locally in close proximity to the enzyme.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cell Line, Tumor
  • Cytoplasm / metabolism
  • D-Amino-Acid Oxidase / metabolism*
  • HeLa Cells
  • Humans
  • Hydrogen Peroxide / metabolism*
  • Mice
  • NIH 3T3 Cells
  • Oxidation-Reduction
  • Recombinant Proteins / metabolism*
  • Signal Transduction / physiology

Substances

  • Recombinant Proteins
  • Hydrogen Peroxide
  • D-Amino-Acid Oxidase