Gao Ya, Lee Jumin, Widmalm Göran, Im Wonpil
School of Mathematics, Physics and Statistics, Shanghai University of Engineering Science, Shanghai 201620, China.
Department of Biological Sciences, Department of Chemistry, and Department of Bioengineering, Lehigh University, Bethlehem, Pennsylvania 18015, United States.
J Phys Chem B. 2020 Jul 16;124(28):5948-5956. doi: 10.1021/acs.jpcb.0c03353. Epub 2020 Jun 30.
Enterobacterial common antigen (ECA) is a surface glycolipid shared by all members of the family. In addition to lipopolysaccharides (LPS), ECA is an important component in the outer membrane (OM) of Gram-negative bacteria, making the OM an effective, selective barrier against the permeation of toxic molecules. Previous modeling and simulation studies represented OMs exclusively with LPS in the outer leaflet. In this work, various ECA molecules were first modeled and incorporated into symmetric bilayers with LPS in different ratios, and all-atom molecular dynamics simulations were conducted to investigate the properties of the mixed bilayers mimicking OM outer leaflets. Dynamic and flexible conformational ensembles are sampled for each ECA/LPS system. Incorporation of ECA (an LPS core-linked form) and ECA (a phosphatidylglycerol-linked form) affects lipid packing and ECA/LPS distributions on the bilayer surface. Hydrophobic thickness and chain order parameter analyses indicate that incorporation of ECA makes the acyl chains of LPS more flexible and disordered and thus increases the area per lipid of LPS. The calculated area per lipid of each ECA/LPS provides a good estimate for building more realistic OMs with different ratios of ECA/LPS, which will be useful in order to characterize their interactions with outer membrane proteins in more realistic OMs.
肠杆菌共同抗原(ECA)是该菌属所有成员共有的一种表面糖脂。除脂多糖(LPS)外,ECA是革兰氏阴性菌外膜(OM)的重要组成部分,使外膜成为抵御有毒分子渗透的有效选择性屏障。以往的建模和模拟研究仅以外叶中的LPS来表示外膜。在这项工作中,首先对各种ECA分子进行建模,并将其以不同比例与LPS整合到对称双层膜中,然后进行全原子分子动力学模拟,以研究模拟外膜外叶的混合双层膜的性质。对每个ECA/LPS系统采样动态灵活的构象集合。掺入ECA(一种LPS核心连接形式)和ECA(一种磷脂酰甘油连接形式)会影响脂质堆积以及ECA/LPS在双层膜表面的分布。疏水厚度和链序参数分析表明,掺入ECA会使LPS的酰基链更灵活且无序,从而增加LPS的脂质分子面积。计算得到的每个ECA/LPS的脂质分子面积为构建具有不同ECA/LPS比例的更真实外膜提供了很好的估计,这对于在更真实的外膜中表征它们与外膜蛋白的相互作用将是有用的。