© 1999 by European Society of Cardiology
Copyright © 1999, European Society of Cardiology
Structure and function of cardiac potassium channels
Department of Molecular Biophysics, Physiology and Pharmacology (VIB), Department of Biochemistry (UIA) University of Antwerp, Universiteitsplein 1 – T4.21, B-2610 Antwerp, Belgium
dsnyders{at}uia.ua.ac.be
* Tel.: +32-3-820-2335; fax: +32-3-820-2541
Recent advances in molecular biology have had a major impact on our understanding of the biophysical and molecular properties of ion channels. This review is focused on cardiac potassium channels which, in general, serve to control and limit cardiac excitability. Approximately 60 K+ channel subunits have been cloned to date. The (evolutionary) oldest potassium channel subunits consist of two transmembrane (Tm) segments with an intervening pore-loop (P). Channels formed by four 2Tm–1P subunits generally function as inwardly rectifying K+-selective channels (KirX.Y): they conduct substantial current near the resting potential but carry little or no current at depolarized potentials. The inward rectifier IK1 and the ligand-gated KATP and KACh channels are composed of such subunits. The second major class of K+ channel subunits consists of six transmembrane segments (S1–S6). The S5–P–S6 section resembles the 2Tm–1P subunit, and the additional membrane-spanning segments (especially the charged S4 segment) endow these 6Tm–1P channels with voltage-dependent gating. For both major families, four subunits assemble into a homo- or heterotetrameric channel, subject to specific subunit–subunit interactions. The 6Tm–1P channels are closed at the resting potential, but activate at different rates upon depolarization to carry sustained or transient outward currents (the latter due to inactivation by different mechanisms). Cardiac cells typically display at least one transient outward current and several delayed rectifiers to control the duration of the action potential. The molecular basis for each of these currents is formed by subunits that belong to different Kvx.y subfamilies and alternative splicing can contribute further to the diversity in native cells. These subunits display distinct pharmacological properties and drug-binding sites have been identified. Additional subunits have evolved by concatenation of two 2Tm–1P subunits (4Tm–2P); dimers of such subunits yield voltage-independent leak channels. A special class of 6Tm–1P subunits encodes the ‘funny’ pacemaker current which activates upon hyperpolarization and carries both Na+ and K+ ions. The regional heterogeneity of K+ currents and action potential duration is explained by the heterogeneity of subunit expression, and significant changes in expression occur in cardiac disease, most frequently a reduction. This electrical remodelling may also be important for novel antiarrhythmic therapeutic strategies. The recent crystallization of a 2Tm–1P channel enhances the outlook for more refined molecular approaches.
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