Gray M A, Tomlins B, Montgomery R A, Williams A J
Department of Cardiac Medicine, University of London, United Kingdom.
Biophys J. 1988 Aug;54(2):233-9. doi: 10.1016/S0006-3495(88)82952-7.
We have studied single-channel conductance fluctuations of K+ channels present in the sarcoplasmic reticulum (SR) membrane systems of rabbit cardiac and skeletal muscle. K+ conductance through the channels is reversibly blocked by gallamine. Conductance block occurs only from the trans side of the channel and is resolved as a smooth reduction in the open state conductance. At a fixed K+ concentration, conduction decreases with increasing gallamine concentration and the data can be fitted to a single-site inhibition scheme. The degree of block seen at a constant gallamine concentration decreases as K+ concentration is increased, indicating competition between gallamine and K+. Gallamine block is voltage dependent, the degree of block increasing with increasing negative holding potential. Quantitative analysis of block yields a zero voltage dissociation constant of 55.3 +/- 16 microM and an effective valence of block of 0.93 +/- 0.12. We conclude that gallamine blocks by interacting with a site or sites located at an electrical distance 30-35% into the voltage drop from the trans side of the channel. This site must have a cross-sectional area of at least 1.2 nm2. The results of this study have been used to modify and extend our view of the structure of the channel's conduction pathway.
我们研究了兔心脏和骨骼肌肌浆网(SR)膜系统中存在的钾离子通道的单通道电导波动情况。通过这些通道的钾离子电导可被加拉明可逆性阻断。电导阻断仅从通道的胞外侧发生,且表现为开放状态电导的平稳降低。在固定的钾离子浓度下,随着加拉明浓度增加,传导性降低,并且数据可拟合为单位点抑制模式。在恒定的加拉明浓度下,随着钾离子浓度增加,观察到的阻断程度降低,表明加拉明与钾离子之间存在竞争。加拉明阻断具有电压依赖性,阻断程度随负性钳制电位增加而增加。对阻断的定量分析得出零电压解离常数为55.3±16微摩尔,有效阻断价为0.93±0.12。我们得出结论,加拉明通过与位于通道胞外侧电压降30 - 35%处的一个或多个位点相互作用而产生阻断。该位点的横截面积必须至少为1.2平方纳米。本研究结果已用于修正和扩展我们对通道传导途径结构的认识。