Evaluation of Hydroxyl Radical Reactivity by Thioether Group Proximity in Model Peptide Backbone: Methionine versus S-Methyl-Cysteine

Hydroxyl radicals (HO center dot) have long been regarded as a major source of cellular damage. The reaction of HO center dot with methionine residues (Met) in peptides and proteins is a complex multistep process. Although the reaction mechanism has been intensively studied, some essential parts remain unsolved. In the present study we examined the reaction of HO center dot generated by ionizing radiation in aqueous solutions under anoxic conditions with two compounds representing the simplest model peptide backbone CH3C(O)NHCHXC(O)NHCH3, where X = CH2CH2SCH3 or CH2SCH3, i.e., the Met derivative in comparison with the cysteine-methylated derivative. We performed the identification and quantification of transient species by pulse radiolysis and final products by LC-MS and high-resolution MS/MS after gamma-radiolysis. The results allowed us to draw for each compound a mechanistic scheme. The fate of the initial one-electron oxidation at the sulfur atom depends on its distance from the peptide backbone and involves transient species of five-membered and/or six-membered ring formations with different heteroatoms present in the backbone as well as quite different rates of deprotonation in forming alpha-(alkylthio)alkyl radicals.

Automated summary

In this study, the complex reaction of hydroxyl radicals with methionine residues in peptides and proteins was investigated using ionizing radiation and pulse radiolysis techniques. The results revealed that the reaction mechanism depends on the distance between the sulfur atom and the peptide backbone, leading to the formation of different transient species and final products.