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Photocatalytic Redox Reactions for In‐Source Peptide Fragmentation
Author(s) -
Qiao Liang,
Bi Hongyan,
Busnel JeanMarc,
Waser Jerome,
Yang Pengyuan,
Girault Hubert H.,
Liu Baohong
Publication year - 2009
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.200802229
Subject(s) - photochemistry , chemistry , redox , fragmentation (computing) , dissociation (chemistry) , ionization , electron transfer dissociation , bond cleavage , excited state , tandem mass spectrometry , mass spectrometry , inorganic chemistry , ion , atomic physics , catalysis , organic chemistry , chromatography , computer science , operating system , physics
In‐source oxidation : In‐source photocatalytic redox reactions for inducing peptide fragmentation are achieved on a TiO 2 ‐derived target plate during laser desorption ionization mass spectrometry in the presence of samples and glucose acting as both an electron donor and a hole conductor (see scheme).In‐source photocatalytic redox reactions based on a photosensitive target plate have been developed to realize peptide fragmentation during laser desorption ionization. Sample peptides and glucose are simply deposited on a spot of sintered TiO 2 nanoparticles. With the irradiation of UV laser on TiO 2 , electrons are excited from the valence to the conduction band, leaving oxidative holes and reductive electrons to drive various in‐source redox reactions. Glucose, working here as a hole scavenger and conductor, can favor both on‐surface reduction and long distance in‐plume oxidation, therefore inducing peptide fragmentation. C α C backbone cleavage was observed to generate a , x fragment decay, while the NC α bond cleavage was also sometimes obtained to induce c , z fragmentation, but was rather weaker. The former dissociation is believed to originate from oxidative routes induced by the valence band holes, based on the oxidation of nitrogen atom at the peptide backbone, including hydrogen‐radical abstraction and electron transfer. In contrast, the latter dissociation is supposed to be the result of reductive processes by the conduction band electrons, which are then rather similar to electron capture dissociation in tandem mass spectrometry.