| Literature DB >> 27059977 |
Christopher J Shaffer1, Jonathan Martens2, Aleš Marek1,3, Jos Oomens2,4, František Tureček5.
Abstract
We report a combined experimental and computational study aimed at elucidating the structure of N-terminal fragment ions of the c type produced by electron transfer dissociation of photo-leucine (L*) peptide ions GL*GGKX. The c 4 ion from GL*GGK is found to retain an intact diazirine ring that undergoes selective photodissociation at 355 nm, followed by backbone cleavage. Infrared multiphoton dissociation action spectra point to the absence in the c 4 ion of a diazoalkane group that could be produced by thermal isomerization of vibrationally hot ions. The c 4 ion from ETD of GL*GGK is assigned an amide structure by a close match of the IRMPD action spectrum and calculated IR absorption. The energetics and kinetics of c 4 ion dissociations are discussed. Graphical Abstract ᅟ.Entities:
Keywords: Electron transfer dissociation; Infrared multiphoton dissociation action spectroscopy; Near-UV photodissociation; Peptide ions; Photoleucine label
Year: 2016 PMID: 27059977 DOI: 10.1007/s13361-016-1390-4
Source DB: PubMed Journal: J Am Soc Mass Spectrom ISSN: 1044-0305 Impact factor: 3.109