Singh C, Sankararamakrishnan R, Subramaniam S, Jakobsson E
Department of Materials Science and Engineering, Beckman Institute for Advanced Science and Technology, University of Illinois, Urbana 61801, USA.
Biophys J. 1996 Nov;71(5):2276-88. doi: 10.1016/S0006-3495(96)79438-9.
This paper describes a molecular dynamics and molecular mechanics study of the solvation and selectivity of the narrow pore and vestibule region of a model-built structure for the voltage-gated sodium channel. The particular structure used was one proposed by Guy and Durell. However, many of the features we saw would likely be shared with other possible models for this channel, such as the one proposed by Lipkind and Fozzard. It was found that the water mobility was reduced in the channel and the water orientations were significantly ordered by the channel environment. Water mobility depended on protein mobility; in a computer experiment in which the protein was artificially frozen, channel water at 300 degrees K was immobilized. Water motions were defined in significant part by a series of discrete moves from one pattern of hydrogen bonding with particular amino acids to another. However, there are so many different hydrogen bonding patterns that a description of the motion in terms of transitions among a small number of discrete states is not appropriate. In the model whose solvation we explored, several charged residues seem to play a particularly significant role in determining solvation and water motions. Based on energy minimization studies, the structure clearly shows selectivity for univalent cations over anions.
本文描述了对电压门控钠通道模型构建结构的狭窄孔道和前庭区域的溶剂化作用及选择性的分子动力学和分子力学研究。所使用的特定结构是由盖伊和杜雷尔提出的。然而,我们所观察到的许多特征可能与该通道的其他可能模型相同,比如利普金德和福扎德提出的模型。研究发现,通道内的水流动性降低,且水的取向因通道环境而显著有序。水的流动性取决于蛋白质的流动性;在一个计算机实验中,蛋白质被人为冻结,300K时通道内的水也被固定住了。水的运动在很大程度上由一系列从与特定氨基酸的一种氢键模式到另一种氢键模式的离散移动所定义。然而,存在如此多不同的氢键模式,以至于用少数离散状态之间的转变来描述运动并不合适。在我们探索其溶剂化作用的模型中,几个带电荷的残基在决定溶剂化作用和水的运动方面似乎起着特别重要的作用。基于能量最小化研究,该结构清楚地显示出对单价阳离子比对阴离子具有选择性。