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近膜电场钙离子脱水

Near-membrane electric field calcium ion dehydration.

作者信息

Barger James P, Dillon Patrick F

机构信息

Department of Physiology, Michigan State University, 567 Wilson Rd., East Lansing, MI 48824, USA.

出版信息

Cell Calcium. 2016 Dec;60(6):415-422. doi: 10.1016/j.ceca.2016.09.006. Epub 2016 Sep 22.

Abstract

The dehydration of ion-water complexes prior to ion channel transit has focused on channel protein-mediated dissociation of water. Ion dehydration by the membrane electric field has not previously been considered. Near membrane electric fields have previously been shown to cause the disassociation of non-covalently bound small molecule-small molecule, small molecule-protein, and protein-protein complexes. It is well known that cosmotropic, structure making ions such as calcium and sodium significantly bind multiple water ions in solution. It is also known that these ions are often not hydrated as they pass through membrane ion channels. Using capillary electrophoresis, the range of electric fields needed to strip water molecules from calcium ions has been measured. Ion migration velocity is a linear function of the electric field. At low electric fields, the migration rate of calcium ion was shown to be linearly related to the applied electric field. Using a form of the Stoke's equation applicable to ion migration, the hydrated calcium radius was found to be 0.334nm, corresponding to a water hydration shell of 5.09 water molecules. At higher electric fields, the slope of the calcium migration velocity as a function of the electric field increased, which was modeled as a decrease in the radius of the migrating ion as the water was removed. Using a tanh function to model the transition of the ion from a hydrated to a stripped state, the transition had a midpoint at 446V/cm, and was 88% complete at 587V/cm with a correlation coefficient of 0.9996. The migration velocity of the stripped calcium ion was found to be a function of both the decrease in radius and an increase in the effective, electronic viscosity of the dipole medium through which the dehydrated ion moved. The size of the electric field needed to dehydrate calcium occurs 6-7nm from the cell membrane. Calcium ions within this distance from the membrane will be devoid of water molecules when they reach the calcium selective channel pore entrances, all known to be approximately 1-2nm from the membrane. No matter what the calcium pore structure, calcium ions reaching the channel entrance will be devoid of a water shell.

摘要

离子通道转运之前离子 - 水复合物的脱水作用主要集中在通道蛋白介导的水的解离。此前尚未考虑膜电场导致的离子脱水。此前已表明,近膜电场会导致非共价结合的小分子 - 小分子、小分子 - 蛋白质和蛋白质 - 蛋白质复合物的解离。众所周知,具有促溶作用、形成结构的离子,如钙和钠,在溶液中会显著结合多个水合离子。还已知这些离子在通过膜离子通道时通常不被水合。利用毛细管电泳,已测量了从钙离子上剥离水分子所需的电场范围。离子迁移速度是电场的线性函数。在低电场下,钙离子的迁移速率与施加的电场呈线性关系。使用适用于离子迁移的斯托克斯方程形式,发现水合钙半径为0.334nm,对应于5.09个水分子的水合壳层。在较高电场下,钙离子迁移速度随电场变化的斜率增加,这被模拟为随着水被去除,迁移离子半径减小。使用双曲正切函数来模拟离子从水合状态到去水状态的转变,该转变的中点在446V/cm,在587V/cm时完成88%,相关系数为0.9996。发现去水钙离子的迁移速度是半径减小以及去水离子移动通过的偶极介质有效电子粘度增加的函数。使钙脱水所需的电场大小出现在距细胞膜6 - 7nm处。距离膜在此距离内的钙离子在到达钙选择性通道孔入口时将没有水分子,所有已知的通道孔入口距膜约1 - 2nm。无论钙孔结构如何,到达通道入口的钙离子都将没有水壳。

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