Selective Functionalization of Peptides with Reactive Fragment Ions.
Ontology highlight
ABSTRACT: Selective binding of highly reactive inorganic fragment ions generated in a mass spectrometer to peptides within surface layers is demonstrated using the sequential mass-selected deposition of the reagents. The closo-dodecaborate fragment ions [B12I11]- and [B12I8S(CN)]- were generated by collision-induced dissociation and bound to three dipeptides: leucyl proline, phenylalanyl proline, and tyrosyl proline. The products formed on the deposition surface were structurally characterized by electrospray ionization tandem mass spectrometry. Deuterium labeling was employed to investigate the reaction. The fragment ion [B12I11]- is demonstrated to react via "first contact" with the vacuum-ori
SUBMITTER: Kawa S
PROVIDER: S-EPMC12333338 | biostudies-literature | 2025 Aug
REPOSITORIES: biostudies-literature
ACCESS DATA