Nakano Minoru, Nakao Hiroyuki, Yoshida Shigeharu, Fukuda Masakazu, Imai Manjiro, Ikeda Keisuke
Department of Biointerface Chemistry, Faculty of Pharmaceutical Sciences, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan.
Graduate School of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan.
J Phys Chem Lett. 2022 Jul 7;13(26):6024-6030. doi: 10.1021/acs.jpclett.2c01080. Epub 2022 Jun 24.
Understanding how lipid dynamics change with membrane curvature is important given that biological membranes constantly change their curvature and morphology through membrane fusion and endo-/exocytosis. Here, we used time-resolved small-angle neutron scattering and time-resolved fluorescence to characterize the properties and dynamics of phospholipids in vesicles with different curvatures. Dissociation of phospholipids from vesicles required traversing an energy barrier comprising positive enthalpy and negative entropy. However, lipids in membranes with high positive curvature have dense acyl chain packing and loose headgroup packing, leading to hydrophobic hydration due to water penetration into the membrane. These properties were found to lower the hydrophobic hydration enhancement associated with phospholipid dissociation and mitigate the acyl chain packing of lipids adjacent to the space created by the lipid dissociation, resulting in an increase in activation entropy. The results of this study provide important insights into the functions of biomembranes in relation to their dynamic structural changes.
鉴于生物膜通过膜融合和内吞/外排作用不断改变其曲率和形态,了解脂质动力学如何随膜曲率变化非常重要。在这里,我们使用时间分辨小角中子散射和时间分辨荧光来表征不同曲率囊泡中磷脂的性质和动力学。磷脂从囊泡中解离需要跨越一个由正焓和负熵组成的能垒。然而,具有高正曲率的膜中的脂质具有密集的酰基链堆积和松散的头基团堆积,由于水渗透到膜中而导致疏水水合作用。发现这些性质降低了与磷脂解离相关的疏水水合增强,并减轻了与脂质解离产生的空间相邻的脂质的酰基链堆积,导致活化熵增加。这项研究的结果为生物膜与其动态结构变化相关的功能提供了重要见解。