Work

Reprogramming the lipid peroxidation product 4-ONE as a chemoselective cleavable crosslinker

Year: 2026

Type: article

Abstract: Lipid peroxidation products modify proteins during oxidative stress, but the residue-pair connectivity and structural consequences of these reactions remain difficult to define. Here, we redefine the lipid peroxidation product 4-oxo-2-nonenal (4-ONE) from a damaging electrophile into a chemoselective Cys-Lys covalent crosslinker. Through a chemoselective, two-step pathway, Michael addition to cysteine activates a latent aldehyde that cyclizes with lysine to form a stable pyrrole linkage under physiological conditions. We show that this chemistry supports late-stage peptide functionalization, macrocyclization and stapling, selective protein modification, and proteome-wide mapping of 4-ONE-reactive lysine and cysteine residues. Additionally, late-stage oxidation converts this pyrrole linkage into an MS-cleavable sulfoxide for site-resolved identification of linked residues through diagnostic link-site-containing fragments, a workflow we name COSMIc (Crosslink Oxidation to Sulfoxide for Mass-Cleavable Interactomics). COSMIc enables detection of structurally informative crosslinks in the human 26S proteasome, where peroxide-induced sulfoxide formation markedly improves fragment assignment and residue-pair confidence. Together, these findings repurpose 4-ONE from a toxic electrophile into a compact, metabolite-derived Cys-Lys crosslinker for covalent mapping and structural proteomics. Lipid peroxidation products modify proteins during oxidative stress, but the residue-pair connectivity and structural consequences of these reactions are difficult to define. Here, the authors employ the lipid peroxidation product 4-oxo-2-nonenal (4-ONE) as a chemoselective Cys-Lys covalent crosslinker, and show that the developed chemistry can be used for late-stage peptide functionalization, macrocyclization and stapling, selective protein modification, and proteome-wide mapping of 4-ONE reactive lysine and cysteine residues.

Source: Nature Communications

DOI: 10.1038/s41467-026-74843-x