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多正离子-阴离子脂质膜相互作用。

Polycation-Anionic Lipid Membrane Interactions.

机构信息

Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Kraków, Poland.

Computational Biomolecular Dynamics Group, Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, 37077 Göttingen, Germany.

出版信息

Langmuir. 2020 Oct 27;36(42):12435-12450. doi: 10.1021/acs.langmuir.0c01062. Epub 2020 Oct 15.

Abstract

Natural or synthetic polycations are used as biocides or as drug/gene carriers. Understanding the interactions between these macromolecules and cell membranes at the molecular level is therefore of great importance for the design of effective polymer biocides or biocompatible polycation-based delivery systems. Until now, details of the processes at the interface between polycations and biological systems have not been fully recognized. In this study, we consider the effect of strong polycations with quaternary ammonium groups on the properties of anionic lipid membranes that we use as a model system for protein-free cell membranes. For this purpose, we employed experimental measurements and atomic-scale molecular dynamics (MD) simulations. MD simulations reveal that the polycations are strongly hydrated in the aqueous phase and do not lose the water shell after adsorption at the bilayer surface. As a result of strong hydration, the polymer chains reside at the phospholipid headgroup and do not penetrate to the acyl chain region. The polycation adsorption involves the formation of anionic lipid-rich domains, and the density of anionic lipids in these domains depends on the length of the polycation chain. We observed the accumulation of anionic lipids only in the leaflet interacting with the polymer, which leads to the formation of compositionally asymmetric domains. Asymmetric adsorption of the polycation on only one leaflet of the anionic membrane strongly affects the membrane properties in the polycation-membrane contact areas: (i) anionic lipid accumulates in the region near the adsorbed polymer, (ii) acyl chain ordering and lipid packing are reduced, which results in a decrease in the thickness of the bilayer, and (iii) polycation-anionic membrane interactions are strongly influenced by the presence and concentration of salt. Our results provide an atomic-scale description of the interactions of polycations with anionic lipid bilayers and are fully supported by the experimental data. The outcomes are important for understanding the correlation of the structure of polycations with their activity on biomembranes.

摘要

天然或合成的聚阳离子被用作杀菌剂或药物/基因载体。因此,了解这些大分子与细胞膜在分子水平上的相互作用对于设计有效的聚合物杀菌剂或基于聚阳离子的生物相容性递送系统非常重要。到目前为止,聚阳离子与生物系统界面的过程细节还没有被完全认识到。在这项研究中,我们考虑了具有季铵基团的强聚阳离子对阴离子脂质膜性质的影响,我们将其用作无蛋白质细胞膜的模型系统。为此,我们采用了实验测量和原子尺度分子动力学(MD)模拟。MD 模拟表明,聚阳离子在水相中有很强的水合作用,在双层表面吸附后不会失去水壳。由于强烈的水合作用,聚合物链位于磷脂头部基团处,不会渗透到酰基链区域。聚阳离子的吸附涉及阴离子脂质丰富的区域的形成,这些区域中阴离子脂质的密度取决于聚阳离子链的长度。我们只观察到阴离子脂质在与聚合物相互作用的单层中的积累,这导致了组成不对称区域的形成。聚阳离子在阴离子膜的一个单层上的不对称吸附强烈影响聚阳离子-膜接触区域的膜性质:(i)阴离子脂质在靠近吸附聚合物的区域积累,(ii)酰基链有序性和脂质堆积减少,导致双层厚度减小,以及(iii)聚阳离子-阴离子膜相互作用强烈受到盐的存在和浓度的影响。我们的结果提供了聚阳离子与阴离子脂质双层相互作用的原子尺度描述,并且完全得到了实验数据的支持。这些结果对于理解聚阳离子结构与其在生物膜上活性的相关性很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c94/7594277/3a40c2770c59/la0c01062_0001.jpg

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