Eaton D C, Brodwick M S
J Gen Physiol. 1980 Jun;75(6):727-50. doi: 10.1085/jgp.75.6.727.
Ba++ ion blocks K+ conductance at concentrations in the nanomolar range. This blockage is time and voltage dependent. From the time dependence it is possible to determine the forward and reverse rate constants for what appears to be an essentially first-order process of Ba++ interaction. The voltage dependence of the rate constants and the dissociation constants place the site of interaction near the middle of the membrane field. Comparison of the efficacy of Ba++ block at various internal K+ concentrations suggests that Ba++ is probably a simple competitive inhibitor of K+ interaction with the K+ conductance. The character of Ba++ block in high external K+ solutions suggests that Ba++ ion may be "knocked-off" the site by inward movement of external K+. Examination of the effects of other divalent cations suggests that the channel may have a closed state with a divalent cation inside the channel. The relative blockage at different temperatures implies a strong interaction between Ba++ and the K+ conductance.
钡离子(Ba++)在纳摩尔浓度范围内会阻断钾离子(K+)电导。这种阻断作用与时间和电压有关。根据时间依赖性,可以确定正向和反向速率常数,这似乎是一个基本为一级的钡离子相互作用过程。速率常数和解离常数的电压依赖性表明相互作用位点位于膜电场的中部附近。比较不同内部钾离子浓度下钡离子阻断的效果表明,钡离子可能是钾离子与钾离子电导相互作用的简单竞争性抑制剂。高外部钾离子溶液中钡离子阻断的特性表明,外部钾离子的向内移动可能会将钡离子从该位点“撞离”。对其他二价阳离子作用的研究表明,通道可能存在一种通道内有二价阳离子的关闭状态。不同温度下的相对阻断作用表明钡离子与钾离子电导之间存在强烈相互作用。