American Chemical Society, Chemical Research in Toxicology, 8(28), p. 1556-1566, 2015
DOI: 10.1021/acs.chemrestox.5b00132
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Urate hydroperoxide is a strong oxidant generated by combination of urate free radical and superoxide. The formation of urate hydroperoxide as an intermediate in urate oxidation is potentially responsible for the pro-oxidant effects of urate in inflammatory disorders, protein degradation, and food decomposition. To understand the molecular mechanisms that sustain the harmful effects of urate in inflammatory and oxidative stress related conditions, we report a detailed structural characterization and reactivity of urate hydroperoxide towards biomolecules. Urate hydroperoxide was synthesized by photo-oxidation and by a myeloperoxidase/hydrogen peroxide/superoxide system. Multiple reaction monitoring (MRM) and MS3 ion fragmentation revealed that urate hydroperoxide from both sources have the same chemical structure. Urate hydroperoxide has a maximum absorption at 308nm, ɛ308nm 6.54 ± 0.38 × 103 M-1.cm-1. This peroxide decays spontaneously with a rate constant of k = 2.80 ± 0.18 × 10-4 s-1, and half-life of 41 min at 22ºC. Urate hydroperoxide undergoes electrochemical reduction at potential values less negative than -0.5V (versus Ag/AgCl). When incubated with taurine, histidine, tryptophan, lysine, methionine, cysteine or glutathione, urate hydroperoxide reacted with methionine, cysteine and glutathione only. The oxidation of these molecules occurred by a two-electron mechanism generating the alcohol hydroxyisourate. No adduct between cysteine or glutathione and urate hydroperoxide was detected. The second order rate constant for the oxidation of glutathione by urate hydroperoxide was 13.7 ± 0.8 M-1 s-1. In conclusion, the oxidation of sulfur containing biomolecules by urate hydroperoxide is likely to be a mechanism for the pro-oxidant and damaging effects of urate in inflammatory and photo-oxidizing processes.