Photoleucine Survives Backbone Cleavage by Electron Transfer Dissociation. A Near-UV Photodissociation and Infrared Multiphoton Dissociation Action Spectroscopy Study

Authors
  • F. Tureček
Publication date 07-2016
Journal Journal of the American Society for Mass Spectrometry
Volume | Issue number 27 | 7
Pages (from-to) 1176-1185
Number of pages 10
Organisations
  • Faculty of Science (FNWI) - Van 't Hoff Institute for Molecular Sciences (HIMS)
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 c4 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 c4 ion of a diazoalkane group that could be produced by thermal isomerization of vibrationally hot ions. The c4 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 c4 ion dissociations are discussed.
Document type Article
Note With supplementary file.
Language English
Published at https://doi.org/10.1007/s13361-016-1390-4
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