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Department of Physiology and Pharmacology, Sackler Medical School, Tel Aviv University, Tel Aviv 69978, Israel

Address correspondence to Bernard Attali, Department of Physiology and Pharmacology, Sackler Medical School, Tel Aviv University, Tel Aviv 69978, Israel. Fax: (972) 3640 9113; email:battali{at}post.tau.ac.il

The pore properties and the reciprocal interactions between permeant ions and the gating of KCNQ channels are poorly understood. Here we used external barium to investigate the permeation characteristics of homomeric KCNQ1 channels. We assessed the Ba²⁺ binding kinetics and the concentration and voltage dependence of Ba²⁺ steady-state block. Our results indicate that extracellular Ba²⁺ exerts a series of complex effects, including a voltage-dependent pore blockade as well as unique gating alterations. External barium interacts with the permeation pathway of KCNQ1 at two discrete and nonsequential sites. (a) A slow deep Ba²⁺ site that occludes the channel pore and could be simulated by a model of voltage-dependent block. (b) A fast superficial Ba²⁺ site that barely contributes to channel block and mostly affects channel gating by shifting rightward the voltage dependence of activation, slowing activation, speeding up deactivation kinetics, and inhibiting channel inactivation. A model of voltage-dependent block cannot predict the complex impact of Ba²⁺ on channel gating in low external K⁺ solutions. Ba²⁺ binding to this superficial site likely modifies the gating transitions states of KCNQ1. Both sites appear to reside in the permeation pathway as high external K⁺ attenuates Ba²⁺ inhibition of channel conductance and abolishes its impact on channel gating. Our data suggest that despite the high degree of homology of the pore region among the various K⁺ channels, KCNQ1 channels display significant structural and functional uniqueness.

Key Words: permeation • ion channels • outer vestibule • inactivation • channel gating

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