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The non-specific role of Mg2+ in ribosomal subunit association: kinetics and equilibrium in the presence of other divalent metal ions.
Authors:A Wishnia  A S Boussert
Institution:Department of Chemistry State University of New York at Stony Brook Stony Brook, N.Y. 11794, U.S.A.
Abstract:The effects of Mg2+, Ca2+, Sr2+, Ba2+, Mn2+, Co2+, Ni2+ and Zn2+ on the kinetics and equilibrium of the association of vacant “tight” ribosomal subunits from Escherichia coli were studied. Increments of Mg2+, Ca2+, Sr2+ and, by and large, Ba2+, to ribosomes dissociated to 30 S and 50 S particles at 1.2 mm-Mg2+ (60 mm-M2+, pH 7.5, 25°C) produce nearly indistinguishable association curves, with midpoints at 1.8 mm total M2+ and complete association to 70 S particles at 4 to 5 mm total M2+ . The association rate constants at 1 mm-Mg2+, 2 mM-M2+ are similar (0.5 × 106 to 0.9 × 106m?1s?1), as are the dissociation rate constants at 1 mm-(Mg2+ + M2+) (0.2 to 0.4 s?1). Mn2+ and Zn2+ increase the degree of association, as well as further aggregation (Zn2+ especially), at lower concentrations than the alkaline earth ions. Co2+ and Ni2+ produce lower degrees of association, by promoting dissociation of the 70 S particle : the association rate constants at 1 mm-Mg2+, 2 mm-M2+ for the transition metal ions are all grouped at 2 × 106 to 3 × 106m?1s?1. Ni2+ also causes a slower inactivation of one or both subunits.The results are compatible with the view that the effects on the rate and equilibrium constants arise from decreases in the electrostatic free energies of the 30 S, 50 S and 70 S particles produced by large-scale, relatively indiscriminate, charge-neutralization “binding” of M2+ , and are difficult if not impossible to reconcile with a specific-sites mode of action of M2+.
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