The ionophore nigericin transports Pb2+ with high activity and selectivity: a comparison to monensin and ionomycin.

Autor: Hamidinia SA; Department of Molecular and Cellular Biochemistry, The Ohio State University, Columbus, Ohio 43210, USA., Tan B, Erdahl WL, Chapman CJ, Taylor RW, Pfeiffer DR
Jazyk: angličtina
Zdroj: Biochemistry [Biochemistry] 2004 Dec 21; Vol. 43 (50), pp. 15956-65.
DOI: 10.1021/bi048175z
Abstrakt: The K(+) ionophore nigericin is shown to be highly effective as an ionophore for Pb(2+) but not other divalent cations, including Cu(2+), Zn(2+), Cd(2+), Mn(2+), Co(2+), Ca(2+), Ni(2+), and Sr(2+). Among this group a minor activity for Cu(2+) transport is seen, while for the others activity is near or below the limit of detection. The selectivity of nigericin for Pb(2+) exceeds that of ionomycin or monensin and arises, at least in part, from a high stability of nigericin-Pb(2+) complexes. Plots of log rate vs log Pb(2+) or log ionophore concentration, together with the pH dependency, indicate that nigericin transports Pb(2+) via the species NigPbOH and by a mechanism that is predominately electroneutral. As with monensin and ionomycin, a minor fraction of activity may be electrogenic, based upon a stimulation of rate that is produced by agents which prevent the formation of transmembrane electrical potentials. Nigericin-catalyzed Pb(2+) transport is not inhibited by physiological concentrations of Ca(2+) or Mg(2+) and is only modestly affected by K(+) and Na(+) concentrations in the range of 0-100 mM. These characteristics, together with higher selectivity and efficiency, suggest that nigericin may be more useful than monensin in the treatment of Pb intoxication.
Databáze: MEDLINE