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一种具有生理组成和膜叶不对称性的脂质膜粗粒化模型。

A Coarse Grained Model for a Lipid Membrane with Physiological Composition and Leaflet Asymmetry.

作者信息

Sharma Satyan, Kim Brian N, Stansfeld Phillip J, Sansom Mark S P, Lindau Manfred

机构信息

Laboratory for Nanoscale Cell Biology, Max-Planck-Institute for Biophysical Chemistry, Göttingen, Germany.

School of Applied and Engineering Physics, Cornell University, Ithaca, New York, United States of America.

出版信息

PLoS One. 2015 Dec 14;10(12):e0144814. doi: 10.1371/journal.pone.0144814. eCollection 2015.

Abstract

The resemblance of lipid membrane models to physiological membranes determines how well molecular dynamics (MD) simulations imitate the dynamic behavior of cell membranes and membrane proteins. Physiological lipid membranes are composed of multiple types of phospholipids, and the leaflet compositions are generally asymmetric. Here we describe an approach for self-assembly of a Coarse-Grained (CG) membrane model with physiological composition and leaflet asymmetry using the MARTINI force field. An initial set-up of two boxes with different types of lipids according to the leaflet asymmetry of mammalian cell membranes stacked with 0.5 nm overlap, reliably resulted in the self-assembly of bilayer membranes with leaflet asymmetry resembling that of physiological mammalian cell membranes. Self-assembly in the presence of a fragment of the plasma membrane protein syntaxin 1A led to spontaneous specific positioning of phosphatidylionositol(4,5)bisphosphate at a positively charged stretch of syntaxin consistent with experimental data. An analogous approach choosing an initial set-up with two concentric shells filled with different lipid types results in successful assembly of a spherical vesicle with asymmetric leaflet composition. Self-assembly of the vesicle in the presence of the synaptic vesicle protein synaptobrevin 2 revealed the correct position of the synaptobrevin transmembrane domain. This is the first CG MD method to form a membrane with physiological lipid composition as well as leaflet asymmetry by self-assembly and will enable unbiased studies of the incorporation and dynamics of membrane proteins in more realistic CG membrane models.

摘要

脂质膜模型与生理膜的相似程度决定了分子动力学(MD)模拟对细胞膜和膜蛋白动态行为的模拟效果。生理脂质膜由多种类型的磷脂组成,且膜层组成通常是不对称的。在此,我们描述了一种使用MARTINI力场自组装具有生理组成和膜层不对称性的粗粒度(CG)膜模型的方法。根据哺乳动物细胞膜的膜层不对称性,将两个装有不同类型脂质的盒子进行初始设置,使其堆叠重叠0.5纳米,可靠地导致了具有类似于生理哺乳动物细胞膜膜层不对称性的双层膜的自组装。在存在质膜蛋白 syntaxin 1A片段的情况下进行自组装,导致磷脂酰肌醇(4,5)二磷酸在 syntaxin的带正电区域自发特异性定位,这与实验数据一致。一种类似的方法是选择初始设置为两个填充有不同脂质类型的同心壳,从而成功组装出具有不对称膜层组成的球形囊泡。在存在突触囊泡蛋白突触结合蛋白2的情况下对囊泡进行自组装,揭示了突触结合蛋白跨膜结构域的正确位置。这是第一种通过自组装形成具有生理脂质组成和膜层不对称性的膜的CG MD方法,将能够在更真实的CG膜模型中对膜蛋白的掺入和动力学进行无偏研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc95/4681583/67eab2af01ad/pone.0144814.g001.jpg

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