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本文引用的文献

1
A permeation theory for single-file ion channels: one- and two-step models.单分子离子通道的渗透理论:一步和两步模型。
J Chem Phys. 2011 Apr 28;134(16):165102. doi: 10.1063/1.3580562.
2
Cycle flux algebra for ion and water flux through the KcsA channel single-file pore links microscopic trajectories and macroscopic observables.离子和水通过 KcsA 单通道的循环通量代数链接微观轨迹和宏观可观察量。
PLoS One. 2011 Jan 31;6(1):e16578. doi: 10.1371/journal.pone.0016578.
3
A mesoscopic approach to understanding the mechanisms underlying the ion permeation on the discrete-state diagram.一种用于理解离散态图上离子渗透潜在机制的介观方法。
J Gen Physiol. 2010 Sep;136(3):363-5. doi: 10.1085/jgp.201010504.
4
Structural mechanism of C-type inactivation in K(+) channels.钾离子通道 C 型失活的结构机制。
Nature. 2010 Jul 8;466(7303):203-8. doi: 10.1038/nature09153.
5
Exploring atomic resolution physiology on a femtosecond to millisecond timescale using molecular dynamics simulations.利用分子动力学模拟在飞秒到毫秒时间尺度上探索原子分辨率生理学。
J Gen Physiol. 2010 Jun;135(6):555-62. doi: 10.1085/jgp.200910373.
6
Principles of conduction and hydrophobic gating in K+ channels.K+ 通道的传导和疏水性门控原理。
Proc Natl Acad Sci U S A. 2010 Mar 30;107(13):5833-8. doi: 10.1073/pnas.0911691107. Epub 2010 Mar 15.
7
Mechanism of potassium-channel selectivity revealed by Na(+) and Li(+) binding sites within the KcsA pore.KcsA孔道内Na(+)和Li(+)结合位点揭示钾通道选择性机制。
Nat Struct Mol Biol. 2009 Dec;16(12):1317-24. doi: 10.1038/nsmb.1703. Epub 2009 Nov 29.
8
Atypical mechanism of conduction in potassium channels.钾通道中的非典型传导机制。
Proc Natl Acad Sci U S A. 2009 Sep 22;106(38):16074-7. doi: 10.1073/pnas.0903226106. Epub 2009 Sep 4.
9
Temperature dependence of proton permeation through a voltage-gated proton channel.质子通过电压门控质子通道渗透的温度依赖性。
J Gen Physiol. 2009 Sep;134(3):191-205. doi: 10.1085/jgp.200910213.
10
A quantitative description of KcsA gating I: macroscopic currents.KcsA通道门控的定量描述I:宏观电流
J Gen Physiol. 2007 Nov;130(5):465-78. doi: 10.1085/jgp.200709843. Epub 2007 Oct 15.

通过 K 通道的开环结构对流动文件中的离子和水分子进行计数。

Counting ion and water molecules in a streaming file through the open-filter structure of the K channel.

机构信息

Department of Molecular Physiology and Biophysics, University of Fukui Faculty of Medical Sciences, Eiheiji-cho, Yoshida-gun, Fukui 910-1193, Japan.

出版信息

J Neurosci. 2011 Aug 24;31(34):12180-8. doi: 10.1523/JNEUROSCI.1377-11.2011.

DOI:10.1523/JNEUROSCI.1377-11.2011
PMID:21865461
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6623228/
Abstract

The mechanisms underlying the selective permeation of ions through channel molecules are a fundamental issue related to understanding how neurons exert their functions. The "knock-on" mechanism, in which multiple ions in the selectivity filter are hit by an incoming ion, is one of the leading concepts. This mechanism has been supported by crystallographic studies that demonstrated ion distribution in the structure of the Streptomyces lividans (KcsA) potassium channel. These still pictures under equilibrium conditions, however, do not provide a snapshot of the actual, ongoing permeation processes. To understand the dynamics of permeation, we determined the ratio of the ion and water flow [the water-ion coupling ratio (CR(w-i))] through the KcsA channel by measuring the streaming potential (V(stream)) electrophysiologically. The V(stream) value was converted to the CR(w-i) value, which reveals how individual ion and water molecules are queued in the narrow and short filter during permeation. At high K(+) concentrations, the CR(w-i) value was 1.0, indicating that turnover between the alternating ion and water arrays occurs in a single-file manner. At low K(+), the CR(w-i) value was increased to a point over 2.2, suggesting that the filter contained mostly one ion at a time. These average behaviors of permeation were kinetically analyzed for a more detailed understanding of the permeation process. Here, we envisioned the permeation as queues of ion and water molecules and sequential transitions between different patterns of arrays. Under physiological conditions, we predicted that the knock-on mechanism may not be predominant.

摘要

离子通过通道分子选择性渗透的机制是理解神经元如何发挥其功能的一个基本问题。“撞击”机制是指多个选择性过滤器中的离子被传入的离子击中,这是一个主要概念。晶体学研究支持了这一机制,该研究表明离子在变形链霉菌(KcsA)钾通道结构中的分布。然而,这些在平衡条件下的静态图片并没有提供实际进行中的渗透过程的快照。为了了解渗透的动态性,我们通过测量流动电势(V(stream))在生理条件下确定了离子和水流通过 KcsA 通道的比例[水-离子偶联比(CR(w-i))]。将 V(stream)值转换为 CR(w-i)值,揭示了在渗透过程中,单个离子和水分子在狭窄而短的过滤器中是如何排队的。在高 K(+)浓度下,CR(w-i)值为 1.0,表明交替的离子和水排列之间的转换以单分子方式发生。在低 K(+)时,CR(w-i)值增加到超过 2.2,表明过滤器一次通常只包含一个离子。为了更详细地了解渗透过程,我们对这些渗透的平均行为进行了动力学分析。在这里,我们将渗透想象为离子和水分子的队列以及不同排列模式之间的顺序转换。在生理条件下,我们预测撞击机制可能不是主要的。