Suppr超能文献

如何解决长链两亲分子与脂质膜相互作用的自由能模拟中的问题:收敛性和局部膜变形

How to tackle the issues in free energy simulations of long amphiphiles interacting with lipid membranes: convergence and local membrane deformations.

作者信息

Filipe Hugo A L, Moreno Maria João, Róg Tomasz, Vattulainen Ilpo, Loura Luís M S

机构信息

Centro de Química de Coimbra, Largo D. Dinis, Rua Larga, 3004-535 Coimbra, Portugal.

出版信息

J Phys Chem B. 2014 Apr 3;118(13):3572-81. doi: 10.1021/jp501622d. Epub 2014 Mar 25.

Abstract

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-1,3-diazol-4-yl-labeled fatty amine, NBD-Cn, 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.

摘要

膜生物物理学中的一大挑战是找到促进药物跨复杂膜结构运输的方法。本着这种精神,我们阐明了与复杂链状分子跨脂质膜自由能计算相关的方法学挑战。为此,作为合适的标准分子,我们考虑7-硝基苯并-2-恶唑-1,3-二氮杂环丁烷-4-基标记的脂肪胺,NBD-Cn,这里将其作为具有不同链长的同系物系列来处理。我们发现膜-水界面区域对自由能计算的细节高度敏感。尽管模拟时间很长,但我们观察到了显著的滞后现象,其原因是两亲分子的烷基链在膜界面中的插入/解吸事件频率较低。当两亲分子从水相中被拉向膜时,滞后现象最为明显,这损害了与实验不符的数据。在沿过渡路径计算距离的伞形采样中的微妙之处也被认为是伪像的潜在原因。采用PGD(拉动几何距离)方案,即计算分子到由膜中所有脂质的平均值确定的参考平面的距离时,我们发现当两亲分子靠近膜时,膜结构会出现明显变形。而采用PGC(拉动几何圆柱体)方法时,变形较弱,该方法的参考平面是根据距离两亲分子半径1.7 nm的圆柱体内的脂质来选择的。重要的是,发现PGC给出的自由能结果在定性上与实验数据一致,而PGD结果则不然。我们得出结论,对于长链两亲分子的自由能分布计算,存在值得关注的理由。膜-水界面是最需要谨慎对待的区域。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验