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Alkali metal ion selectivity of the hemocyanin channel
Authors:Ximena Cecchi  Ramon Latorre  Osvaldo Alvarez
Institution:(1) Departmento de Biologia, Facultad de Ciencias Basicas y Farmaceuticas, Universidad de Chile, Santiago, Chile;(2) Department of Physiology and Biophysics, Harvard Medical School, 02115 Boston, Massachusetts
Abstract:Summary The selectivity of the hemocyanin channel was measured for alkali metal ions and ammonium. Permeability ratios relative to K+ measured from biionic potentials were: NH 4 + (1.52)>Rb+ (1.05)>K+ (1.0)>Cs+ (0.89)>Na+ (0.81)>Li+ (0.35). Single-channel ion conductance was a saturating function of ion concentration regardless of the cation present in the bathing medium. Maximal conductances were 270, 267, 215, 176, 170 and 37 ps for K+, Rb+, NH 4 + , Cs+, Na+ and Li+, respectively. Current-voltage curves for the different monovalent cations were measured and described using a threebarrier model previously used to explain the voltage dependence of the ldquoinstantaneousrdquo channel conductance (Cecchi, Alvarez & Latorre, 1981). In this way, binding and peak energies were estimated for the different ions. Considering the energy peaks as transition states between the ion and the channel, it is concluded that they follow Eisenman's selectivity sequences XI (cis peak, i.e., Li+>Na+>K+>Rb+>Cs+; highest field strength), VII (central peak) and II (trans peak). The cis side was that to which hemocyanin was added and was electrically ground. The binding energies, on the other hand, follow Eisenman's series XI for strong electric field sites. Binding of NH 4 + to the cis-well suggests that the orientation of the ligands in the site is tetrahedric.
Keywords:hemocyanin  channel selectivity  energy barriers  ion transport
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