Ravoo B J, Weringa W D, Engberts J B
Department of Organic and Molecular Inorganic Chemistry and Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, 9747 AG Groningen, The Netherlands.
Biophys J. 1999 Jan;76(1 Pt 1):374-86. doi: 10.1016/S0006-3495(99)77204-8.
Membrane fusion has been examined in a model system of small unilamellar vesicles of synthetic lipids that can be oligomerized through the lipid headgroups. The oligomerization can be induced either in both bilayer leaflets or in the inner leaflet exclusively. Oligomerization leads to denser lipid headgroup packing, with concomitant reduction of lipid lateral diffusion and membrane permeability. As evidenced by lipid mixing assays, electron microscopy, and light scattering, calcium-induced fusion of the bilayer vesicles is strongly retarded and inhibited by oligomerization. Remarkably, oligomerization of only the inner leaflet of the bilayer is already sufficient to affect fusion. The efficiency of inhibition and retardation of fusion critically depend on the relative amount of oligomeric lipid present, on the concentration of calcium ions, and on temperature. Implications for the mechanism of bilayer membrane fusion are discussed in terms of lipid lateral diffusion and membrane curvature effects.
在一个由合成脂质构成的小单层囊泡模型系统中研究了膜融合,这些囊泡可通过脂质头部基团进行寡聚化。寡聚化既可以在两个双层小叶中诱导,也可以仅在内小叶中诱导。寡聚化导致脂质头部基团堆积更紧密,同时脂质横向扩散和膜通透性降低。脂质混合测定、电子显微镜和光散射表明,钙诱导的双层囊泡融合受到寡聚化的强烈阻碍和抑制。值得注意的是,仅双层内小叶的寡聚化就足以影响融合。融合抑制和阻碍的效率关键取决于存在的寡聚脂质的相对量、钙离子浓度和温度。从脂质横向扩散和膜曲率效应方面讨论了对双层膜融合机制的影响。