Gas-phase ion-molecule reactions using regioselectively generated radical cations to model oxidative damage and probe radical sites in peptides

Abstract

Collision induced dissociation (CID) of sodiated peptide derivatives containing a nitrate ester functionality was used to regiospecifically generate three isomeric radicals of the model peptide Bz-Ala-Gly-OMe corresponding to radicals formed at: C^α of the alanine residue [4+Na]⁺; C^α of the glycine residue [5+Na]⁺; and the side chain of alanine [6+Na]⁺. The ion-molecule reactions of these peptide radicals were examined to model oxidative damage to peptides and to probe whether the radical sites maintain their integrity or whether they isomerise via intramolecular hydrogen atom transfer (HAT). Only [6+Na]⁺ is reactive towards O₂, forming the peroxyl radical [7+Na]⁺, which loses O₂, HO˙ and HO₂˙ under CID. The radical ion [7 + Na]⁺ abstracts a hydrogen atom from 4-fluorothiophenol to form the hydroperoxide [8+Na]⁺, which upon CID fragments via the combined loss of HO˙ and CH₂O. In contrast, all three of the isomeric sodiated radicals react with NO˙ and NO₂˙ to form adducts. CID of the NO adducts only regenerates the radicals viaNO˙ loss, thus providing no structural information. In contrast, CID of the NO₂ adducts gives rise to a range of product ions and the spectra are different for each of the three adducts, suggesting that the isomeric radicals [4+Na]⁺, [5+Na]⁺ and [6+Na]⁺ are produced as discrete species. Finally, CID of the NO₂ adducts was used to probe the rearrangement of the radicals [4+Na]⁺, [5+Na]⁺ and [6+Na]⁺ prior to their reaction with NO₂˙: [6 + Na]⁺ rearranges to a mixture of [4+Na]⁺ and [5+Na]⁺ while [5+Na]⁺ rearranges to [4+Na]⁺.