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首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >How To Tackle the Issues in Free Energy Simulations of Long Amphiphiles Interacting with Lipid Membranes: Convergence and Local Membrane Deformations
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How To Tackle the Issues in Free Energy Simulations of Long Amphiphiles Interacting with Lipid Membranes: Convergence and Local Membrane Deformations

机译:如何解决长两亲分子与脂质膜相互作用的自由能模拟中的问题:会聚和局部膜变形

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One of the great challenges in membrane biophysics is to find a means to foster the transport of drugs across complex membrane structures. In this spirit, we elucidate methodological challenges associated with free energy computations of complex chainlike molecules across lipid membranes. As an appropriate standard molecule to this end, we consider 7-nitrobenz-2-oxa-l,3-diazol-4-yl-labeled fatty amine, NBD-C,,, which is here dealt with as a homologous series with varying chain lengths. We found the membrane-water interface region to be highly sensitive to details in free energy computations. Despite considerable simulation times, we observed substantial hysteresis, the cause being the small frequency of insertion/desorption events of the amphiphile's alkyl chain in the membrane interface. The hysteresis was most pronounced when the amphiphile was pulled from water to the membrane and compromised the data that were not in line with experiments. The subtleties in umbrella sampling for computing distance along the transition path were also observed to be potential causes of artifacts. With the PGD (pull geometry distance) scheme, in which the distance from the molecule was computed to a reference plane determined by an average over all lipids in the membrane, we found marked deformations in membrane structure when the amphiphile was close to the membrane. The deformations were weaker with the PGC (pull geometry cylinder) method, where the reference plane is chosen based on lipids that are within a cylinder of radius 1.7 nm from the amphiphile. Importantly, the free energy results given by PGC were found to be qualitatively consistent with experimental data, while the PGD results were not. We conclude that with long amphiphiles there is reason for concern with regard to computations of their free energy profiles. The membrane-water interface is the region where the greatest care is warranted.
机译:膜生物物理学的一大挑战是找到一种促进药物跨复杂膜结构运输的方法。本着这种精神,我们阐明了与跨脂膜的复杂链状分子的自由能计算相关的方法挑战。为此,作为合适的标准分子,我们考虑了7-硝基苯-2-氧杂-1,3-二氮杂-4-基标记的脂肪胺NBD-C,在此将其视为具有不同序列的同源序列链长。我们发现膜-水界面区域对自由能计算中的细节高度敏感。尽管有相当长的模拟时间,我们仍观察到了很大的滞后现象,其原因是两亲性烷基链在膜界面中的插入/解吸事件发生频率较低。当两亲物从水中拉到膜上并破坏了与实验不一致的数据时,磁滞现象最为明显。伞形采样中用于计算沿过渡路径的距离的细微之处也被认为是造成伪影的潜在原因。使用PGD(拉式几何距离)方案,其中计算分子到参考平面的距离,参考平面是由膜中所有脂质的平均值确定的,当两亲物靠近膜时,我们发现膜结构发生了明显变形。使用PGC(拉几何圆柱体)方法的变形较弱,其中参考平面是根据距两亲物半径1.7 nm的圆柱体内的脂质选择的。重要的是,发现PGC给出的自由能结果在质量上与实验数据一致,而PGD结果却与之不符。我们得出的结论是,对于长的两亲物,其自由能分布的计算值得关注。膜-水界面是需要最大程度注意的区域。

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