4.4 Article

Peptide dissociation patterns in secondary ion mass spectrometry under large argon cluster ion bombardment

Journal

RAPID COMMUNICATIONS IN MASS SPECTROMETRY
Volume 27, Issue 13, Pages 1490-1496

Publisher

WILEY
DOI: 10.1002/rcm.6599

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Funding

  1. Grants-in-Aid for Scientific Research [23246012] Funding Source: KAKEN

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RATIONALE The analysis of organic and biological substances by secondary ion mass spectrometry (SIMS) has greatly benefited from the use of cluster ions as primary bombarding species. Thereby, depth profiling and three-dimensional (3D) imaging of such systems became feasible. Large Arn+ cluster ions may constitute a further improvement in this direction. METHODS To explore this option, large Arn+ cluster ions (with n similar to 1500 Ar atoms per cluster) were used to investigate the emission of positive secondary ions from two peptide specimens (angiotensin I and bradykinin) by orthogonal time-of-flight SIMS using bombarding energies 6, 10 and 14keV. RESULTS For both peptides, the protonated molecular ion is observed in the mass spectra. In addition, distinct fragmentation patterns were observed; these indicate that fragment ions under Ar cluster irradiation form primarily via cleavage of bonds along the peptide backbone whereas the rapture of side chains occurs much less frequently. These features appear to be similar to low-energy collision-induced dissociation pathways. CONCLUSIONS Tentatively, these findings can then be ascribed to the concerted action of the large number of Ar atoms in the impact zone of cluster at the surface: these low-energy Ar species (with an average energy of few eV) may effect the cleavage of the peptide bonds and lead, eventually, to the emission of the fragment ions. Copyright (c) 2013 John Wiley & Sons, Ltd.

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