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关于使钠通道激活与失活解偶联的突变。

On mutations that uncouple sodium channel activation from inactivation.

作者信息

Goldman L

机构信息

Department of Physiology, School of Medicine, University of Maryland, Baltimore, Maryland 21201, USA.

出版信息

Biophys J. 1999 May;76(5):2553-9. doi: 10.1016/S0006-3495(99)77408-4.

Abstract

Computations on sodium channel gating were conducted using a closed-open-inactivated coupled kinetic scheme. The time constant of inactivation (tauh) derives a voltage dependency from coupling to voltage-dependent activation even when rate constants between inactivated and other states are strictly voltage independent. The derived voltage dependency does not require any physical, molecular link between the structures responsible for inactivation and the charges producing voltage-dependent activation. The only requirement is that the closed to inactivated rate constant (kCI) differs from the open to inactivated (kOI), consistent with experimental results. A number of mutations and other treatments uncouple sodium channel activation and inactivation in that the voltage dependency of tauh is substantially reduced while voltage-dependent activation persists. However, a clear basis for uncoupling has not been described. A variety of experimental results are accounted for just by changes in the difference between kOI and kCI. In wild type channels, kOI > kCI and inactivation develops with a delay whose time constant is just that for channel opening. Mutations that reduce the kOI - kCI difference reduce the amplitude of the delay process and the derived voltage dependency of tauh. If kOI = kCI, inactivation develops as a single exponential (no matter what the number of closed states), activation and inactivation become independent, parallel processes, and any voltage dependency of tauh is then entirely intrinsic to inactivation. If kOI < kCI, inactivation develops as the sum of exponentials, tauh at negative potentials speeds and then slows with more positive potentials. These predicted kOI < kCI effects have all been seen experimentally (O'Leary, M.E., L.-Q. Chen, R.G. Kallen, and R. Horn. 1995. J. Gen. Physiol. 106: 641-658). An open to closed rate constant of zero also removes the derived voltage dependency of tauh, but activation and inactivation are still coupled and the inactivation delay remains.

摘要

利用一种关闭-开放-失活耦合动力学方案对钠通道门控进行了计算。失活时间常数(tauh)从与电压依赖性激活的耦合中获得电压依赖性,即使失活状态与其他状态之间的速率常数严格与电压无关。所推导的电压依赖性并不要求负责失活的结构与产生电压依赖性激活的电荷之间存在任何物理的、分子的联系。唯一的要求是从关闭到失活的速率常数(kCI)不同于从开放到失活的速率常数(kOI),这与实验结果一致。许多突变和其他处理会使钠通道激活和失活解偶联,即tauh的电压依赖性显著降低,而电压依赖性激活仍然存在。然而,尚未描述解偶联的明确基础。仅通过kOI和kCI之间差异的变化就能解释各种实验结果。在野生型通道中,kOI > kCI,失活延迟出现,其时间常数就是通道开放的时间常数。减小kOI - kCI差异的突变会减小延迟过程的幅度以及所推导的tauh的电压依赖性。如果kOI = kCI,失活以单指数形式发展(无论关闭状态的数量如何),激活和失活成为独立的、平行的过程,并且tauh的任何电压依赖性随后完全是失活所固有的。如果kOI < kCI,失活以指数之和的形式发展,负电位下的tauh加快,然后随着电位更正而减慢。这些预测的kOI < kCI效应在实验中均已观察到(O'Leary, M.E., L.-Q. Chen, R.G. Kallen, and R. Horn. 1995. J. Gen. Physiol. 106: 641 - 658)。开放到关闭的速率常数为零也会消除所推导的tauh的电压依赖性,但激活和失活仍然耦合,失活延迟仍然存在。

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