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Multiply-charged cations derived from electrospray of bovine ubiquitin and horse skeletal muscle apomyoglobin have been subjected to reactions with anions derived from glow discharge ionization of perfluoro-1,3-dimethylcyclohexane. The results are compared with data obtained from proton transfer reactions with strong gaseous neutral bases. Ion/ion reaction rates are shown to be linearly related to the square of the charge on the protein ion, as expected based on a simple capture collision model. Cationic products with charge as low as +1 could be readily formed via ion/ion reactions, whereas efforts to produce such low charge states via ion/molecule reactions have proved unsuccessful. Ion/ion proton transfer reactions appear to be an effective means of reducing charge on highly charged proteins to arbitrarily low charge states. In addition to proton transfer, ion/ion recombination has also been observed. The propensity for proton transfer versus anion attachment to the cation is highly dependent upon the identity of the anion.
Stephenson et al. (Mon,) studied this question.