Methionine oxidation selectively enhances T cell reactivity against a melanoma antigen

The impact of the peptide amino acids side-chain modifications on the immunological recognition has been scarcely explored. We investigate here the effect of methionine oxidation on the antigenicity of the melanoma immunodominant peptide 369-YMDGTMSQV-377 (YMD). Using CD8+ T cell activation assays, we found that the antigenicity of the sulfoxide form is higher when compared to the YMD peptide. This is consistent with free energy computations performed on HLA-A∗02:01/YMD/TCR complex showing that this is lowered upon oxidation, paired with a steep increase in order at atomic level. Oxidized YMD forms were identified at the melanoma cell surface by LC-MS/MS analysis. These results demonstrate that methionine oxidation in the antigenic peptides may generate altered peptide ligands with increased antigenicity, and that this oxidation may occur in vivo, opening up the possibility that high-affinity CD8+ T cells might be naturally primed in the course of melanoma progression, as a result of immunosurveillance. [Display omitted] •Oxidation of the Met residues in YMD tyrosinase yields sulfoxides/sulfone peptides•LC-MS analysis detects oxidized YMD-HLA∗02:01 complexes at the cell surface•YMD-restricted CD8+ T cell clones assays reveal that oxidation increases activation•ΔG computations indicate tighter binding upon oxidation in HLA-YMD-TCR complex Immunology; Biochemistry; Cancer