Marquês Joaquim T, Viana Ana S, De Almeida Rodrigo F M
Centro de Química e Bioquímica, Faculdade de Ciências da Universidade de Lisboa, Ed. C8, Campo Grande 1749-016, Lisboa, Portugal.
Biochim Biophys Acta. 2011 Jan;1808(1):405-14. doi: 10.1016/j.bbamem.2010.10.006. Epub 2010 Oct 15.
Ethanol-lipid bilayer interactions have been a recurrent theme in membrane biophysics, due to their contribution to the understanding of membrane structure and dynamics. The main purpose of this study was to assess the interplay between membrane lateral heterogeneity and ethanol effects. This was achieved by in situ atomic force microscopy, following the changes induced by sequential ethanol additions on supported lipid bilayers formed in the absence of alcohol. Binary phospholipid mixtures with a single gel phase, dipalmitoylphosphatidylcholine (DPPC)/cholesterol, gel/fluid phase coexistence DPPC/dioleoylphosphatidylcholine (DOPC), and ternary lipid mixtures containing cholesterol, mimicking lipid rafts (DOPC/DPPC/cholesterol and DOPC/sphingomyelin/cholesterol), i.e., with liquid ordered/liquid disordered (ld/lo) phase separation, were investigated. For all compositions studied, and in two different solid supports, mica and silicon, domain formation or rearrangement accompanied by lipid bilayer thinning and expansion was observed. In the case of gel/fluid coexistence, low ethanol concentrations lead to a marked thinning of the fluid but not of the gel domains. In the case of ld/lo all the bilayer thins simultaneously by a similar extent. In both cases, only the more disordered phase expanded significantly, indicating that ethanol increases the proportion of disordered domains. Water/bilayer interfacial tension variation and freezing point depression, inducing acyl chain disordering (including opening and looping), tilting, and interdigitation, are probably the main cause for the observed changes. The results presented herein demonstrate that ethanol influences the bilayer properties according to membrane lateral organization.
乙醇与脂质双层的相互作用一直是膜生物物理学中反复研究的主题,因为它们有助于理解膜的结构和动力学。本研究的主要目的是评估膜横向异质性与乙醇效应之间的相互作用。这是通过原位原子力显微镜实现的,跟踪在无醇条件下形成的支持脂质双层上逐次添加乙醇所引起的变化。研究了具有单一凝胶相的二元磷脂混合物(二棕榈酰磷脂酰胆碱(DPPC)/胆固醇)、凝胶/流体相共存的DPPC/二油酰磷脂酰胆碱(DOPC),以及含有胆固醇的三元脂质混合物(模拟脂筏,即DOPC/DPPC/胆固醇和DOPC/鞘磷脂/胆固醇),也就是具有液相有序/液相无序(ld/lo)相分离的情况。对于所有研究的组成,以及在云母和硅这两种不同的固体支持物上,均观察到了伴随脂质双层变薄和扩张的结构域形成或重排。在凝胶/流体共存的情况下,低浓度乙醇会导致流体结构域显著变薄,但凝胶结构域不会。在ld/lo的情况下,所有双层同时以相似程度变薄。在这两种情况下,只有更无序的相显著扩张,这表明乙醇增加了无序结构域的比例。水/双层界面张力变化和凝固点降低,导致酰基链无序化(包括打开和成环)、倾斜和叉指化,可能是观察到的变化的主要原因。本文给出的结果表明,乙醇根据膜的横向组织影响双层性质。