Almgren M
Department of Physical Chemistry, Uppsala University, Box 532, S-751 21, Uppsala, Sweden.
Biochim Biophys Acta. 2000 Nov 23;1508(1-2):146-63. doi: 10.1016/s0005-2736(00)00309-6.
The solubilization of lipid bilayers by surfactants is accompanied by morphological changes of the bilayer and the emergence of mixed micelles. From a phase equilibrium perspective, the lipid/surfactant/water system is in a two-phase area during the solubilization: a phase containing mixed micelles is in equilibrium with bilayer structures of the lamellar phase. In some cases three phases are present, the single micelle phase replaced by a concentrated and a dilute solution phase. In the case of non-ionic surfactants, the lipid bilayers reach saturation when mixed micelles, often flexible rod-like or thread-like, start to form in the aqueous solution, at a constant chemical potential of the surfactant. The composition of the bilayers also remains fixed during the dissolution. The phase behavior encountered with many charged surfactants is different. The lamellar phase becomes destabilized at a certain content of surfactant in the membrane, and then disintegrates, forming mixed micelles, or a hexagonal phase, or an intermediate phase. Defective bilayer intermediates, such as perforated vesicles, have been found in several systems, mainly with charged surfactants. The perforated membranes, in some systems, go over into thread-like micelles via lace-like structures, often without a clear two-phase region. Intermediates in the form of disks, either micelles or bilayer fragments, have been observed in several cases. Most noteworthy are the planar and circular disks found in systems containing a large fraction of cholesterol in the bilayer. Bile salts are a special class of surfactants that seem to break down the bilayer at low additions. Originally, disk-like mixed micelles were conjectured, with polar membrane lipids building the disk, and the bile salts covering the hydrophobic rim. Later work has shown that flexible cylinders are the dominant intermediates also in these systems, even if the disk-like structures have been re-established as transients in the transformation from mixed micelles to vesicles.
表面活性剂使脂质双层溶解的过程伴随着双层结构的形态变化以及混合胶束的出现。从相平衡的角度来看,在溶解过程中脂质/表面活性剂/水体系处于两相区:含有混合胶束的相与层状相的双层结构处于平衡状态。在某些情况下会出现三相,单胶束相被浓溶液相和稀溶液相取代。对于非离子表面活性剂,当在恒定的表面活性剂化学势下,水溶液中开始形成通常为柔性棒状或线状的混合胶束时,脂质双层达到饱和。在溶解过程中双层的组成也保持固定。许多带电表面活性剂所表现出的相行为则不同。当膜中表面活性剂达到一定含量时,层状相会变得不稳定,然后解体,形成混合胶束、六方相或中间相。在几个体系中发现了有缺陷的双层中间体,如穿孔囊泡,主要是在带电表面活性剂体系中。在某些体系中,穿孔膜会通过花边状结构转变为线状胶束,通常没有明显的两相区。在一些情况下观察到了盘状中间体,无论是胶束还是双层片段。最值得注意的是在双层中含有大量胆固醇的体系中发现的平面圆盘和圆形盘。胆汁盐是一类特殊的表面活性剂,似乎在低添加量时就能破坏双层结构。最初推测存在盘状混合胶束,极性膜脂构成盘状结构,胆汁盐覆盖疏水边缘。后来的研究表明,即使盘状结构在从混合胶束到囊泡的转变过程中作为瞬态重新形成,柔性圆柱体也是这些体系中的主要中间体。