Abstract
Within the reactive oxygen species (ROS) generated by cellular metabolisms, hydroxyl radicals (HO(•)) play an important role, being the most aggressive towards biomolecules. The reactions of HO(•) with methionine residues (Met) in peptides and proteins have been intensively studied, but some fundamental aspects remain unsolved. In the present study we examined the biomimetic model made of Ac-Met-OMe, as the simplest model peptide backbone, and of HO(•) generated by ionizing radiation in aqueous solutions under anoxic conditions. We performed the identification and quantification of transient species by pulse radiolysis and of final products by LC-MS and high-resolution MS/MS after γ-radiolysis. By parallel photochemical experiments, using 3-carboxybenzophenone (CB) triplet with the model peptide, we compared the outcomes in terms of short-lived intermediates and stable product identification. The result is a detailed mechanistic scheme of Met oxidation by HO(•), and by CB triplets allowed for assigning transient species to the pathways of products formation.