Journal of the American Society for Mass Spectrometry

, Volume 16, Issue 5, pp 779–791

A comparison of data analysis methods for determining gas phase stabilities by cid: Alkali metal complexes of polyether ionophore antibiotics


  • Matthew W. Forbes
    • Institute for Marine BiosciencesNational Research Council
    • Institute for Marine BiosciencesNational Research Council
  • Gregory J. Francis
    • Department of ChemistryYork University, Center for Research in Mass Spectrometry
  • Diethard K. Böhme
    • Department of ChemistryYork University, Center for Research in Mass Spectrometry

DOI: 10.1016/j.jasms.2005.01.025

Cite this article as:
Forbes, M.W., Volmer, D.A., Francis, G.J. et al. J Am Soc Mass Spectrom (2005) 16: 779. doi:10.1016/j.jasms.2005.01.025


The gas phase stabilities of Group I metal complexes of the polyether ionophore antibiotics lasalocid and monensin were investigated by collision induced dissociation mass spectrometry. Electrospray ionization was used with a triple quadrupole mass spectrometer for the determination of threshold dissociation energies upon application of increasing collision energies. Various data analysis techniques for the determination of dissociation energies are discussed to assess the most suitable method for determining the stabilities of the ionophore-metal complexes studied here. In all cases only the relative stabilities of different complexes may be obtained by the method presented in this study, which does not assess absolute gas phase dissociation energies. Correction factors have been applied, however, to account for the energy conversion during collisions of different metal complexes and the varying degrees of freedom of different sized ligands, allowing for the comparison of the stabilities of different ionophores with like-metals. The measured threshold dissociation energies were compared with respect to the ionic radius of the metal cation, revealing a maximum stability for the K+ complexes of both lasalocid and monensin. A striking decrease in the stabilities of the Rb+ and Cs+ complexes was observed and is believed to be related to a decreasing degree of coordination that the ionophores can accomplish with the larger metals.

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© American Society for Mass Spectrometry 2005