Unidad de Biofisica (Centro Mixto CSIC-UPV/EHU), Leioa 48940, Spain.
FEBS Lett. 2010 May 3;584(9):1824-9. doi: 10.1016/j.febslet.2010.01.039. Epub 2010 Jan 26.
One of the fundamental properties of biological membranes is the high lateral integrity provided by the lipid bilayer, the structural core and the foundation of their barrier function. This tensile strength is due to the intrinsic properties of amphiphilic lipid molecules, which spontaneously self-assemble into a stable bilayer structure due to the hydrophobic effect. In the highly dynamic life of cellular membranes systems, however, this integrity has to be regularly compromised. One of the emerging puzzles is the mechanism of localized rupture of lipid monolayer, the formation of tiny hydrophobic patches and flipping of lipid tails between closely apposed monolayers. The energy cost of such processes is prohibitively high, unless cooperative deformations in a small membrane patch are carefully organized. Here we review the latest experimental and theoretical data on how such deformations can be conducted, specifically describing how elastic stresses yield tilting of lipids leading to cooperative restructuring of lipid monolayers. Proteins specializing in membrane remodeling assemble into closely packed circular complexes to arrange these deformations in time and space.
生物膜的基本特性之一是脂质双层提供的高横向完整性,这是其屏障功能的结构核心和基础。这种拉伸强度归因于两亲性脂质分子的固有特性,由于疏水作用,这些脂质分子自发自组装成稳定的双层结构。然而,在细胞膜系统高度动态的生命中,这种完整性必须经常受到损害。一个新兴的难题是脂质单层局部破裂、形成微小疏水区以及脂质尾部在紧密相邻单层之间翻转的机制。除非仔细组织小膜片中的协同变形,否则这些过程的能量成本高得令人望而却步。在这里,我们回顾了关于这些变形如何进行的最新实验和理论数据,特别是描述了弹性应力如何导致脂质倾斜,从而导致脂质单层的协同重构。专门从事膜重塑的蛋白质组装成紧密堆积的圆形复合物,以便及时和空间上安排这些变形。