Department of Anesthesiology, Pharmacology and Therapeutics, University of British Columbia, Vancouver, British Columbia V6T 1Z3, Canada.
J Gen Physiol. 2013 Apr;141(4):431-43. doi: 10.1085/jgp.201210942. Epub 2013 Mar 11.
The human ether-á-go-go-related gene (hERG) K(+) channel encodes the pore-forming α subunit of the rapid delayed rectifier current, IKr, and has unique activation gating kinetics, in that the α subunit of the channel activates and deactivates very slowly, which focuses the role of IKr current to a critical period during action potential repolarization in the heart. Despite its physiological importance, fundamental mechanistic properties of hERG channel activation gating remain unclear, including how voltage-sensor movement rate limits pore opening. Here, we study this directly by recording voltage-sensor domain currents in mammalian cells for the first time and measuring the rates of voltage-sensor modification by [2-(trimethylammonium)ethyl] methanethiosulfonate chloride (MTSET). Gating currents recorded from hERG channels expressed in mammalian tsA201 cells using low resistance pipettes show two charge systems, defined as Q(1) and Q(2), with V(1/2)'s of -55.7 (equivalent charge, z = 1.60) and -54.2 mV (z = 1.30), respectively, with the Q(2) charge system carrying approximately two thirds of the overall gating charge. The time constants for charge movement at 0 mV were 2.5 and 36.2 ms for Q(1) and Q(2), decreasing to 4.3 ms for Q(2) at +60 mV, an order of magnitude faster than the time constants of ionic current appearance at these potentials. The voltage and time dependence of Q2 movement closely correlated with the rate of MTSET modification of I521C in the outermost region of the S4 segment, which had a V(1/2) of -64 mV and time constants of 36 ± 8.5 ms and 11.6 ± 6.3 ms at 0 and +60 mV, respectively. Modeling of Q(1) and Q(2) charge systems showed that a minimal scheme of three transitions is sufficient to account for the experimental findings. These data point to activation steps further downstream of voltage-sensor movement that provide the major delays to pore opening in hERG channels.
人类醚-á-去甲肾上腺素相关基因 (hERG) K(+) 通道编码快速延迟整流电流的孔形成α亚基,IKr,并具有独特的激活门控动力学,即通道的α亚基非常缓慢地激活和失活,这使得 IKr 电流的作用集中在心脏动作电位复极化的关键时期。尽管其具有生理重要性,但 hERG 通道激活门控的基本机制特性仍不清楚,包括电压传感器运动速度如何限制孔的打开。在这里,我们首次通过记录哺乳动物细胞中的电压传感器结构域电流并测量 [2-(三甲基铵)乙基]甲硫磺酸氯盐 (MTSET) 对电压传感器修饰的速率来直接研究这一点。使用低电阻玻璃微电极从在哺乳动物 tsA201 细胞中表达的 hERG 通道记录门控电流显示出两个电荷系统,定义为 Q(1) 和 Q(2),V(1/2)' 分别为 -55.7(等效电荷,z = 1.60)和 -54.2 mV(z = 1.30),其中 Q(2) 电荷系统携带约三分之二的总门控电荷。在 0 mV 时电荷移动的时间常数为 Q(1) 和 Q(2) 分别为 2.5 和 36.2 ms,在 +60 mV 时 Q(2) 减小至 4.3 ms,比这些电位下离子电流出现的时间常数快一个数量级。Q2 运动的电压和时间依赖性与最外层 S4 段 I521C 的 MTSET 修饰速率密切相关,其 V(1/2)为 -64 mV,在 0 和 +60 mV 时的时间常数分别为 36 ± 8.5 ms 和 11.6 ± 6.3 ms。对 Q(1) 和 Q(2) 电荷系统的建模表明,三个跃迁的最小方案足以解释实验结果。这些数据表明,激活步骤进一步落后于电压传感器的运动,这为 hERG 通道中孔的打开提供了主要的延迟。