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© The Rockefeller University Press, 0022-1295/1998//211/ $5.00
Journal of General Physiology, Volume 112, Number 2, 1998


research-article

Coupled Ion Movement Underlies Rectification in an Inward-Rectifier K+ Channel



Maria Spassova and Zhe Lu

From the Department of Physiology, University of Pennsylvania, Philadelphia, Pennsylvania 19104


ABSTRACT
We studied block of the internal pore of the ROMK1 inward-rectifier K+ channel by Mg2+ and five quaternary ammoniums (tetramethylammonium, tetraethylammonium, tetrapropylammonium, tetrabutylammonium, and tetrapentylammonium). The apparent affinity of these blockers varied as a function of membrane voltage. As a consequence, the channel conducted K+ current more efficiently in the inward than the outward direction; i.e., inward rectification. Although the size of some monovalent quaternary ammoniums is rather large, the z{delta} values (which measure voltage dependence of their binding to the pore) were near unity in symmetric 100 mM K+. Furthermore, we observed that not only the apparent affinities of the blockers themselves, but also their dependence on membrane voltage (or z{delta}), varied as a function of the concentration of extracellular K+. These results suggest that there is energetic coupling between the binding of blocking and permeating (K+) ions, and that the voltage dependence of channel blockade results, at least in part, from the movement of K+ ions in the electrical field. A further quantitative analysis of the results explains why the complex phenomenon of inward rectification depends on both membrane voltage and the equilibrium potential for K+.

Key Words: inward-rectifier K+ channel • rectification • ionic blocker • magnesium • tetraethylammonium


Address correspondence to Dr. Zhe Lu, University of Pennsylvania, Department of Physiology, D302A Richards Building, 3700 Hamilton Walk, Philadelphia, PA 19104-6085. Fax: 215-573-5851; E-mail: zhelu{at}mail.med.upenn.edu


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