Department of Cell Biology, Scripps Research Institute, La Jolla, California, USA.
Biophys J. 2010 Jul 21;99(2):517-25. doi: 10.1016/j.bpj.2010.04.036.
A complete mechanistic understanding of membrane-localized processes in vesicular transport, such as membrane budding and fission, requires their reconstitution with biochemically-defined components from a biochemically-defined substrate. Supported bilayers formed by vesicle fusion represent an attractive substrate for this purpose. However, conventional supported bilayers lack a sufficient membrane reservoir to recreate membrane budding and fission events. We describe the formation of supported bilayers with excess membrane reservoir (SUPER) templates from the fusion of liposomes containing negatively charged lipids on silica beads under high-ionic-strength conditions. Using a fluorescence microscopy-based assay to monitor early and late stages of supported bilayer formation, we show that an increase in ionic strength leads to an increase in the rates of liposome adsorption and subsequent fusion during formation of supported bilayers. The two rates, however, increase disproportionally, leading to accumulation of excess reservoir with an increase in ionic strength. SUPER templates allow the seamless application of microscopy-based assays to analyze membrane-localized processes together with sedimentation-based assays to isolate vesicular and nonvesicular products released from the membrane. The results presented here emphasize the general utility of these templates for analyzing vesicular and nonvesicular transport processes.
要全面了解囊泡运输中膜定位过程(如膜出芽和裂变)的机制,需要用生物化学定义的底物中的生化定义组件进行重建。通过囊泡融合形成的支撑双层代表了一种有吸引力的底物。然而,传统的支撑双层缺乏足够的膜储备来重新创建膜出芽和裂变事件。我们描述了在高离子强度条件下,带负电荷的脂质的脂质体在硅胶珠上融合,形成具有过量膜储备(SUPER)模板的支撑双层。使用基于荧光显微镜的测定法来监测支撑双层形成的早期和晚期阶段,我们表明离子强度的增加会导致在形成支撑双层时,脂质体吸附和随后融合的速率增加。然而,这两个速率不成比例地增加,导致在离子强度增加时积累了过量的储备。SUPER 模板允许无缝应用基于显微镜的测定法来分析膜定位过程,以及基于沉降的测定法来分离从膜释放的囊泡和非囊泡产物。这里呈现的结果强调了这些模板在分析囊泡和非囊泡运输过程中的普遍适用性。