Theory and Bio-systems, Max Planck Institute of Colloids and Interfaces, Science Park Golm, 14424 Potsdam, Germany.
J Chem Phys. 2018 Aug 28;149(8):084901. doi: 10.1063/1.5038427.
Glycolipids such as GM1 have bulky head groups consisting of several monosaccharides. When these lipids are added to phospholipid bilayers, they generate large membrane curvatures even for small compositional asymmetries between the two leaflets of the bilayers. On the micrometer scale, these bilayer asymmetries lead to the spontaneous tubulation of giant vesicles as recently observed by optical microscopy. Here, we study these mixed membranes on the nanometer scale using coarse-grained molecular simulations. The membrane composition is defined by the mole fractions and of the large-head lipid in the two leaflets of the bilayer. Symmetric membranes are obtained for = ≡ , and asymmetric ones for ≠ . In both cases, we compute the density and stress profiles across the membranes. The stress profiles are used to identify the tensionless states of the membranes. Symmetric and tensionless bilayers are found to be stable within the whole composition range 0 ≤ ≤ 1. For these symmetric bilayers, both the area compressibility modulus and the bending rigidity are found to vary non-monotonically with the leaflet mole fraction . For asymmetric bilayers, we compute the product of bending rigidity and spontaneous curvature from the first moment of the stress profile and determine the bending rigidities of the asymmetric membranes using the -dependent rigidities of the single leaflets. When we combine these results, the compositional asymmetry - is found to generate the spontaneous curvature ( - )/(0.63 ) with the membrane thickness ≃ 4 nm. Therefore, the spontaneous curvature increases linearly with the compositional asymmetry. Furthermore, the small compositional asymmetry - = 0.04 leads to the large spontaneous curvature 1/(63 nm) and the increased asymmetry - = 0.2 generates the huge spontaneous curvature 1/(13 nm). These large values of the spontaneous curvature will facilitate future simulation studies of various membrane processes such as bud formation and nanoparticle engulfment.
糖脂(如 GM1)具有由几个单糖组成的庞大头部基团。当这些脂质被添加到磷脂双层膜中时,即使双层膜的两个叶之间存在小的组成不对称性,它们也会产生大的膜曲率。在微米尺度上,这些双层膜不对称性导致了巨大囊泡的自发管化,这是最近光学显微镜观察到的。在这里,我们使用粗粒分子模拟在纳米尺度上研究这些混合膜。膜的组成由双层膜两个叶的大单头脂质的摩尔分数 和 定义。对于 = ≡ ,得到对称膜,对于 ≠ ,得到不对称膜。在这两种情况下,我们都计算了膜的密度和应力分布。应力分布用于识别膜的无张力状态。对称和无张力的双层膜在整个组成范围内 0 ≤ ≤ 1 都是稳定的。对于这些对称双层膜,我们发现面积压缩模量和弯曲刚度都随叶摩尔分数 非单调变化。对于不对称双层膜,我们从应力分布的第一矩计算弯曲刚度和自发曲率的乘积,并使用单叶的 - 依赖刚性确定不对称膜的弯曲刚度。当我们结合这些结果时,发现弯曲刚度和自发曲率的乘积为 ( - )/(0.63 ),其中膜厚度 ≃ 4nm。因此,自发曲率随组成不对称性 - 线性增加。此外,小的组成不对称性 - = 0.04 导致大的自发曲率 1/(63nm),而增加的不对称性 - = 0.2 产生了巨大的自发曲率 1/(13nm)。这些大的自发曲率将有助于未来对各种膜过程(如芽形成和纳米颗粒吞噬)的模拟研究。