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
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.