Department of Biological, Chemical and Physical Sciences, Center of Molecular Study of Soft Condensed Matter, Illinois Institute of Technology, Chicago, Illinois 60616, United States.
Langmuir. 2012 Feb 7;28(5):2842-8. doi: 10.1021/la204623u. Epub 2012 Jan 26.
The physical properties of lipid bilayers can be remodeled by a variety of environmental factors. Here we investigate using molecular dynamics simulations the specific effects of nanoscopic substrates or external contact points on lipid membranes. We expose palmitoyl-oleoyl phosphatidylcholine bilayers unilaterally and separately to various model nanosized substrates differing in surface hydroxyl densities. We find that a surface hydroxyl density as low as 10% is sufficient to keep the bilayer juxtaposed to the substrate. The bilayer interacts with the substrate indirectly through multiple layers of water molecules; however, despite such buffered interaction, the bilayers exhibit certain properties different from unsupported bilayers. The substrates modify transverse lipid fluctuations, charge density profiles, and lipid diffusion rates, although differently in the two leaflets, which creates an asymmetry between bilayer leaflets. Other properties that include lipid cross-sectional areas, component volumes, and order parameters are minimally affected. The extent of asymmetry that we observe between bilayer leaflets is well beyond what has been reported for bilayers adsorbed on infinite solid supports. This is perhaps because the bilayers are much closer to our nanosized finite supports than to infinite solid supports, resulting in a stronger support-bilayer electrostatic coupling. The exposure of membranes to nanoscopic contact points, therefore, cannot be considered as a simple linear interpolation between unsupported membranes and membranes supported on infinite supports. In the biological context, this suggests that the exposure of membranes to nonintercalating proteins, such as those belonging to the cytoskeleton, should not always be considered as passive nonconsequential interactions.
脂质双层的物理性质可以被多种环境因素重塑。在这里,我们通过分子动力学模拟研究了纳米级底物或外部接触点对脂质膜的具体影响。我们分别将棕榈酰-油酰磷脂酰胆碱双层单侧暴露于不同表面羟基密度的各种模型纳米级底物。我们发现,表面羟基密度低至 10%就足以使双层与底物并置。双层通过多层水分子与底物间接相互作用;然而,尽管存在这种缓冲相互作用,双层仍表现出与无支撑双层不同的某些性质。底物会改变横向脂质波动、电荷密度分布和脂质扩散率,尽管在双层的两个叶状片中不同,但这会在双层叶状片中产生不对称性。其他性质,包括脂质横截面积、组成体积和有序参数,受影响最小。我们观察到的双层叶状片中的不对称程度远远超过了在无限固体支持物上吸附的双层的报道。这可能是因为双层与我们的纳米级有限支持物比与无限固体支持物更接近,从而导致更强的支持物-双层静电耦合。因此,将膜暴露于纳米级接触点不能被视为无支撑膜和支撑在无限支持物上的膜之间的简单线性插值。在生物学背景下,这表明将膜暴露于非嵌入蛋白(如细胞骨架蛋白)不应总是被视为被动的无后果的相互作用。