AN ELECTROSPRAY MASS-SPECTROMETRIC AND VOLTAMMETRIC STUDY OF HORSE HEART CYTOCHROME-C IN THE PRESENCE OF METAL-IONS

Studies on cytochrome c in the presence of a range of biologically ess ential (Ca2+, Mg2+, Zn2+, Ni2+ and Co2+) and toxic (MeHg+ Cd2+ and Pb2 +) metal ions have been undertaken by both cyclic voltammetry at a 4,4 '-bipyridyl disulfide modified gold electrode and by electrospray mass spectrometry. Some bases for comparison of data obtained by the two t echniques were achieved by compromising solvent systems and electrolyt e (buffer) concentrations with which these techniques are commonly use d. The most compatible solvent/electrolyte system for these techniques was found to be 65:35 water:isopropanol with acetic acid, and/or ammo nium acetate being added to provide acid, electrolyte and buffer. The electrospray mass spectra of cytochrome c obtained at increased acid c oncentrations showed a shift in the spectral profile to lower mass-to- charge ratios, indicating an increase in the charge density of cytochr ome c, The addition of metal salts to the electrospray solution produc ed metal ion adduction, the number of metal ions binding to the protei n increasing with metal salt concentration. However, the adduction of metal ions to cytochrome c did not alter the overall charge of the pro tein. Electrospray mass spectrometry and cyclic voltammetry showed tha t the heme group was neither lost nor replaced by any of the added met al ions. Voltammetric measurements indicate that no preferential bindi ng of metal ions to either the Fe(III) or Fe(II) oxidation states occu rs, since the reversible potential obtained from voltammetric measurem ents did not change following the metal salt additions. (C) 1998 Elsev ier Science S.A.