Nitric oxide and nitroxides can act as efficient scavengers of protein-derived free radicals.

Nitric oxide (()NO) may act as either a pro-oxidant or an antioxidant in biological systems. Although ()NO and nitroxide radicals react slowly with most molecules, they react at near diffusion-controlled rates with other radicals and may therefore be efficient protective agents. This study assessed the ability of ()NO and nitroxides to intercept specific protein-derived radicals and compared the efficacy of these species. Three protein radical systems were investigated as follows: BSA-derived radicals generated via radical transfer from H(2)O(2)-activated horseradish peroxidase, radicals formed on myoglobin via reaction with H(2)O(2), and carbon-centered radicals formed from amino acid hydroperoxides on exposure to Fe(2+)-EDTA. In each case, radicals were generated in the absence or presence of ()NO or nitroxides of different size and charge. Concentration-dependent loss of the protein radicals was detected by electron paramagnetic resonance with both ()NO and nitroxides and time-dependent consumption of ()NO using an ()NO electrode. The protein oxidation product dityrosine was significantly reduced by ()NO and nitroxides, and 3,4-dihydroxyphenylalanine levels were reduced by nitroxides but not ()NO. Overall, these studies demonstrate that ()NO and nitroxides are efficient near-stoichiometric scavengers of protein radicals and, hence, are potential protective agents against protein oxidation reactions and resulting damage. These reactions show little dependence on nitroxide structure or charge.