DECLUSTERING AND FRAGMENTATION OF PROTEIN IONS FROM AN ELECTROSPRAY ION-SOURCE

Authors
Citation
Ba. Thomson, DECLUSTERING AND FRAGMENTATION OF PROTEIN IONS FROM AN ELECTROSPRAY ION-SOURCE, Journal of the American Society for Mass Spectrometry, 8(10), 1997, pp. 1053-1058
Citations number
11
Categorie Soggetti
Chemistry Physical","Chemistry Analytical",Spectroscopy
ISSN journal
10440305
Volume
8
Issue
10
Year of publication
1997
Pages
1053 - 1058
Database
ISI
SICI code
1044-0305(1997)8:10<1053:DAFOPI>2.0.ZU;2-X
Abstract
A triple quadrupole mass spectrometer with a high pressure collision c ell has been used to explore the declustering and fragmentation proces ses that may occur in the vacuum interface region of an electrospray o r ionspray ion source. Using apomyoglobin as a model protein compound, collisional processes in Q2 were used to elucidate possible mechanism s which could occur in the orifice-skimmer region to affect the observ ed charge state distribution. The results indicate that charge loss or gain through collisional loss of a proton or electron does not occur; rather, higher collision energy results in better declustering of low er charge state ions, and fragmentation of higher charge state ions. T he net result is an apparent shift toward lower charge state as the co llision energy in the free jet region is increased. In addition, the d ata suggest that a mixture of heavily clustered monomers and possibly dimers and multimers are present in the expansion from ion source into vacuum, and it is this mixture which is acted on by the declustering field to produce the observed mass spectrum. The presence of these ''s uperclusters'' needs to be considered in any theory of ion desorption and transport processes in the source and interface region. (C) 1997 A merican Society for Mass Spectrometry.