Loboda A, Armstrong C M
Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104. USA.
Biophys J. 2001 Aug;81(2):905-16. doi: 10.1016/S0006-3495(01)75750-5.
We examined the late transitions in the activation sequence of potassium channels by analyzing gating currents of mutant Shaker IR channels and using the potassium channel blocker 4-aminopyridine (4AP). Gating currents were recorded from a double mutant of Shaker that was nonconducting (W434F mutation) and had the late gating transitions shifted to the right on the voltage axis (L382C mutation), thus separating the late transitions from the early ones. 4AP applied to the double mutant blocked the final transition and made possible novel observations of the isolated intermediate transitions, the ones that immediately precede the final opening of the channel. These transitions, which have not been well characterized previously, produce a distinct fast component in the gating current tails. Two intermediate transitions contribute to the fast component and carry 23% of the total gating charge. The effect of 4AP is well modeled as a selective block of the final gating transition, which opens the channel. The final transition contributes approximately 5% of the total gating charge.
我们通过分析突变型Shaker IR通道的门控电流并使用钾通道阻滞剂4-氨基吡啶(4AP),研究了钾通道激活序列中的晚期转变。门控电流是从一个非传导性的Shaker双突变体(W434F突变)记录的,该突变体在电压轴上的晚期门控转变向右移动(L382C突变),从而将晚期转变与早期转变分开。应用于双突变体的4AP阻断了最终转变,并使得对孤立的中间转变进行新的观察成为可能,这些中间转变紧接在通道最终开放之前。这些以前没有得到很好表征的转变,在门控电流尾部产生一个明显的快速成分。两个中间转变对快速成分有贡献,并携带总门控电荷的23%。4AP的作用可以很好地模拟为对打开通道的最终门控转变的选择性阻断。最终转变贡献了总门控电荷的约5%。