Journal article
Gas-phase formation and reactions of radical cations of guanosine, deoxyguanosine and their homodimers and heterodimers
L Feketeová, E Yuriev, JD Orbell, GN Khairallah, RAJ O'Hair
International Journal of Mass Spectrometry | ELSEVIER | Published : 2011
Abstract
Electrospray ionisation of methanolic solutions containing a mixture of the nucleoside deoxyguanosine, dG, incubated with Cu(NO3)2 resulted in the formation of a range of ions, including doubly charged copper nucleoside complexes [CuIIdGn]2+, with n ranging from 2 to 10. Collision-induced dissociation of these complexes proceeds via a number of different pathways that depend on the size of the cluster, n. When n = 3, monomeric radical cations are formed via redox processes. When n = 4, dimeric radical cations are formed. Related complexes are formed for the nucleoside guanosine, Gs, and these [CuIIGsn]2+ complexes fragment in similar fashions to their [CuIIdG n]2+ counterparts. A key finding..
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Funding Acknowledgements
RAJO and LF thank the ARC for financial support via the ARC Centre of Excellence in Free Radical Chemistry and Biotechnology. LF thanks the ARC for the award of an APD. The authors gratefully acknowledge the generous allocation of computing time from the Victorian Partnership for Advanced Computing (VPAC) Facility.