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使用弱酸来确定氢离子通过短杆菌肽通道传导时的整体扩散限制。

Use of weak acids to determine the bulk diffusion limitation of H+ ion conductance through the gramicidin channel.

作者信息

Decker E R, Levitt D G

机构信息

Department of Physiology, University of Minnesota, Minneapolis 55455.

出版信息

Biophys J. 1988 Jan;53(1):25-32. doi: 10.1016/S0006-3495(88)83062-5.

Abstract

The addition of 2 M formic acid at pH 3.75 increased the single channel H+ ion conductance of gramicidin channels 12-fold at 200 mV. Other weak acids (acetic, lactic, oxalic) produce a similar, but smaller increase. Formic acid (and other weak acids) also blocks the K+ conductance at pH 3.75, but not at pH 6.0 when the anion form predominates. This increased H+ conductance and K+ block can be explained by formic acid (HF) binding to the mouth of the gramicidin channel (Km = 1 M) and providing a source of H+ ions. A kinetic model is derived, based on the equilibrium binding of formic acid to the channel mouth, that quantitatively predicts the conductance for different mixtures of H+, K+, and formic acid. The binding of the neutral formic acid to the mouth of the gramicidin channel is directly supported by the observation that a neutral molecule with a similar structure, formamide (and malonamide and acrylamide), blocks the K+ conductance at pH 6.0. The H+ conductance in the presence of formic acid provides a lower bound for the intrinsic conductance of the gramicidin channel when there is no diffusion limitation at the channel mouth. The 12-fold increase in conductance produced by formic acid suggests that greater than 90% of the total resistance to H+ results from diffusion limitation in the bulk solution.

摘要

在pH 3.75的条件下添加2 M甲酸,可使短杆菌肽通道的单通道H⁺离子电导在200 mV时增加12倍。其他弱酸(乙酸、乳酸、草酸)也会产生类似但较小的增加。甲酸(以及其他弱酸)在pH 3.75时也会阻断K⁺电导,但在pH 6.0且阴离子形式占主导时则不会。这种增加的H⁺电导和K⁺阻断现象可以用甲酸(HF)结合到短杆菌肽通道口(Km = 1 M)并提供H⁺离子源来解释。基于甲酸与通道口的平衡结合推导出一个动力学模型,该模型定量预测了不同H⁺、K⁺和甲酸混合物的电导。中性甲酸与短杆菌肽通道口的结合得到了直接支持,因为观察到具有相似结构的中性分子甲酰胺(以及丙二酰胺和丙烯酰胺)在pH 6.0时会阻断K⁺电导。当通道口不存在扩散限制时,甲酸存在下的H⁺电导为短杆菌肽通道的本征电导提供了下限。甲酸使电导增加12倍表明,对H⁺的总电阻中超过90%来自本体溶液中的扩散限制。

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