Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1981750 | FEBS Open Bio | 2014 | 5 Pages |
•We developed a simple HPLC method to determine the oxidative status of human peroxiredoxin 2 (Prx2).•tert-Butyl hydroperoxide irreversibly hyperoxidizes cysteine residues of Prx2 more readily than H2O2.•Hyperoxidized Prx2 is more hydrophobic than the native form in red blood cells.
Peroxiredoxin 2 (Prx2) is the third most abundant protein in red blood cells (RBCs). In this study, we have succeeded in implementing the rapid and simultaneous detection of the hyperoxidized (Prx2-SO2/3) and reduced (Prx2-SH) forms of Prx2 in human RBCs using reverse phase high-performance liquid chromatography. The detection of a peak corresponding to Prx2-SO2/3 was clearly observed following treatment of tert-butyl hydroperoxide (t-BHP), but not H2O2, and was found to be dose-dependent. The identity of the peak was confirmed as Prx2 by immunoblotting and mass spectrometry analysis. Our results suggest that t-BHP hyperoxidizes cysteine residues in Prx2 more readily than H2O2, and that accumulation of hyperoxidized Prx2 might reflect disruption of redox homeostasis in RBCs.