Hesketh J C, Fedida D
Department of Physiology, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z3.
Am J Physiol. 1999 Nov;277(5):H1956-66. doi: 10.1152/ajpheart.1999.277.5.H1956.
On-gating current from the Kv1.5 cardiac delayed rectifier K(+) channel expressed in HEK-293 cells was separated into two distinct charge systems, Q(1) and Q(2), obtained from double Boltzmann fits to the charge-voltage relationship. Q(1) and Q(2) had characteristic voltage dependence and sensitivity with half-activation potentials of -29.6 +/- 1.6 and -2.19 +/- 2.09 mV and effective valences of 1. 87 +/- 0.15 and 5.53 +/- 0.27 e(-), respectively. The contribution to total gating charge was 0.20 +/- 0.04 for Q(1) and 0.80 +/- 0.04 (n = 5) for Q(2). At intermediate depolarizations, heteromorphic gating current waveforms resulted from relatively equal contributions from Q(1) and Q(2), but with widely different kinetics. Prepulses to -20 mV moved only Q(1), simplified on-gating currents, and allowed rapid Q(2) movement. Voltage-dependent on-gating current recovery in the presence of 4-aminopyridine (1 mM) suggested a sequentially coupled movement of the two charge systems during channel activation. This allowed the construction of a linear five-state model of Q(1) and Q(2) gating charge movement, which predicted experimental on-gating currents over a wide potential range. Such models are useful in determining state-dependent mechanisms of open and closed channel block of cardiac K(+) channels.
在HEK - 293细胞中表达的Kv1.5心脏延迟整流钾通道的门控电流被分离为两个不同的电荷系统,Q(1)和Q(2),这是通过对电荷 - 电压关系进行双玻尔兹曼拟合得到的。Q(1)和Q(2)具有特征性的电压依赖性和敏感性,半激活电位分别为 - 29.6±1.6和 - 2.19±2.09 mV,有效价分别为1.87±0.15和5.53±0.27 e(-)。Q(1)对总门控电荷的贡献为0.20±0.04,Q(2)为0.80±0.04(n = 5)。在中等去极化时,异形门控电流波形是由Q(1)和Q(2)相对相等的贡献产生的,但动力学差异很大。预脉冲至 - 20 mV仅移动Q(1),简化了门控电流,并允许Q(2)快速移动。在存在4 - 氨基吡啶(1 mM)的情况下,电压依赖性门控电流恢复表明在通道激活期间两个电荷系统的顺序耦合运动。这允许构建Q(1)和Q(2)门控电荷运动的线性五态模型,该模型预测了在很宽的电位范围内的实验性门控电流。这样的模型有助于确定心脏钾通道开放和关闭通道阻滞的状态依赖性机制。