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首页> 外文期刊>The Journal of Chemical Physics >Asymmetry of lipid bilayers induced by monovalent salt:Atomistic molecular-dynamics study
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Asymmetry of lipid bilayers induced by monovalent salt:Atomistic molecular-dynamics study

机译:一价盐诱导脂质双层的不对称性:原子分子动力学研究

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Interactions between salt ions and lipid components of biological membranes are essential for the structure,stability,and functions of the membranes.The specific ionic composition of aqueous buffers inside and outside of the cell is known to differ considerably.To model such a situation we perform atomistic molecular-dynamics (MD) simulations of a single-component phosphatidylcholine lipid bilayer which separates two aqueous reservoirs with and without NaCl salt.To implement the difference in electrolyte composition near two membrane sides,a double bilayer setup (i.e.,two bilayers in a simulation box) is employed.It turns out that monovalent salt,being in contact with one leaflet only,induces a pronounced asymmetry in the structural,electrostatic,and dynamical properties of bilayer leaflets after 50 ns of MD simulations.Binding of sodium ions to the carbonyl region of the leaflet which is in contact with salt results in the formation of "Na-lipids" complexes and,correspondingly,reduces mobility of lipids of this leaflet.In turn,attractive interactions of chloride ions (mainly located in the aqueous phase close to the water-lipid interface) with choline lipid groups lead to a substantial (more vertical) reorientation of postphatidylcholine headgroups of the leaflet adjoined to salt.The difference in headgroup orientation on two sides of a bilayer,being coupled with salt-induced reorientation of water dipoles,leads to a notable asymmetry in the charge-density profiles and electrostatic potentials of bilayer constitutes of the two leaflets.Although the overall charge density of the bilayer is found to be almost insensitive to the presence of salt,a slight asymmetry in the charge distribution between the two bilayer leaflets results in a nonzero potential difference of about 85 mV between the two water phases.Thus,a transmembrane potential of the order of the membrane potential in a cell can arise without ionic charge imbalance between two aqueous compartments.
机译:盐离子与生物膜脂质成分之间的相互作用对于膜的结构,稳定性和功能至关重要。已知细胞内部和外部的水性缓冲液的特定离子组成存在很大差异。为了模拟这种情况,我们执行单个分子磷脂酰胆碱脂质双层的原子分子分子动力学(MD)模拟,该双层分离两个有和没有NaCl盐的含水储层。要实现两个膜侧面附近电解质成分的差异,需要一个双层双层结构(即,一个双层中的两个双层结果表明,单价盐仅与一张小叶接触,在50 ns的MD模拟后会引起双层小叶的结构,静电和动力学性质出现明显的不对称性。与盐接触的小叶的羰基区域导致形成“ Na-脂质”复合物,并相应地减少反过来,氯离子(主要位于靠近水-脂质界面的水相中)与胆碱脂质基团的有吸引力的相互作用导致邻接的小叶后胆碱胆碱头基的实质性(更垂直)取向双层两侧的头基取向不同,再加上盐引起的水偶极子重新取向,导致两张小叶的电荷密度分布和双层的静电势显着不对称。发现双层的总电荷密度几乎对盐的存在不敏感,两个双层小叶之间的电荷分布略有不对称导致两个水相之间的非零电势差约为85 mV。因此,跨膜在两个水性隔室之间没有离子电荷不平衡的情况下,可以产生电池中膜电位数量级的电位。

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