French R J, Shoukimas J J
J Gen Physiol. 1985 May;85(5):669-98. doi: 10.1085/jgp.85.5.669.
We have studied the block of potassium channels in voltage-clamped squid giant axons by nine organic and alkali cations, in order to learn how the channel selects among entering ions. When added to the internal solution, all of the ions blocked the channels, with inside-positive voltages enhancing the block. Cesium blocked the channels from the outside as well, with inside-negative voltages favoring block. We compared the depths to which different ions entered the channel by estimating the "apparent electrical distance" to the blocking site. Simulations with a three-barrier, double-occupancy model showed that the "apparent electrical distance," expressed as a fraction of the total transmembrane voltage, appears to be less than the actual value if the blocking ion can pass completely through the channel. These calculations strengthen our conclusion that sodium and cesium block at sites further into the channel than those occupied by lithium and the organic blockers. Our results, considered together with earlier work, demonstrate that the depth to which an ion can readily penetrate into the potassium channel depends both on its size and on the specific chemical groups on its molecular surface. The addition of hydroxyl groups to alkyl chains on a quaternary ammonium ion can both decrease the strength of binding and allow deeper penetration into the channel. For alkali cations, the degree of hydration is probably crucial in determining how far an ion penetrates. Lithium, the most strongly hydrated, appeared not to penetrate as far as sodium and cesium. Our data suggest that there are, minimally, four ion binding sites in the permeation pathway of the potassium channel, with simultaneous occupancy of at least two.
我们研究了九种有机阳离子和碱金属阳离子对电压钳制的枪乌贼巨大轴突中钾通道的阻断作用,以了解通道如何在进入的离子中进行选择。当添加到内部溶液中时,所有离子都能阻断通道,膜内为正电压时会增强阻断作用。铯也能从外部阻断通道,膜内为负电压时有利于阻断。我们通过估计到阻断位点的“表观电距离”来比较不同离子进入通道的深度。用三屏障、双占据模型进行的模拟表明,如果阻断离子能完全穿过通道,那么以总跨膜电压的分数表示的“表观电距离”似乎小于实际值。这些计算强化了我们的结论,即钠和铯的阻断位点比锂和有机阻断剂所占据的位点更深入通道内部。我们的结果与早期工作相结合表明,离子能够轻易穿透钾通道的深度既取决于其大小,也取决于其分子表面的特定化学基团。在季铵离子的烷基链上添加羟基既能降低结合强度,又能使离子更深入地穿透通道。对于碱金属阳离子,水合程度可能对决定离子穿透的深度至关重要。水合程度最强的锂似乎没有钠和铯穿透得那么深。我们的数据表明,钾通道通透途径中至少有四个离子结合位点,且至少同时占据两个位点。