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Bilayer Edges Catalyze Supported Lipid Bilayer Formation

机译:双层边缘催化支持的脂质双层形成

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摘要

Supported lipid bilayers (SLB) are important for the study of membrane-based phenomena and as coatings for biosensors. Nevertheless, there is a fundamental lack of understanding of the process by which they form from vesicles in solution. We report insights into the mechanism of SLB formation by vesicle adsorption using temperature-controlled time-resolved fluorescence microscopy at low vesicle concentrations. First, lipid accumulates on the surface at a constant rate up to ∼0.8 of SLB coverage. Then, as patches of SLB nucleate and spread, the rate of accumulation increases. At a coverage of ∼1.5 × SLB, excess vesicles desorb as SLB patches rapidly coalesce into a continuous SLB. Variable surface fluorescence immediately before SLB patch formation argues against the existence of a critical vesicle density necessary for rupture. The accelerating rate of accumulation and the widespread, abrupt loss of vesicles coincide with the emergence and disappearance of patch edges. We conclude that SLB edges enhance vesicle adhesion to the surface and induce vesicle rupture, thus playing a key role in the formation of continuous SLB.
机译:支持的脂质双层(SLB)对于研究基于膜的现象以及作为生物传感器的涂层非常重要。然而,从根本上缺乏对它们在溶液中由囊泡形成的过程的理解。我们报告洞察到SLB形成机理的研究在低囊泡浓度下使用温度控制的时间分辨荧光显微镜技术进行囊泡吸附。首先,脂质以恒定的速率累积在表面上,直至SLB覆盖率约为0.8。然后,随着SLB斑块的成核和扩散,积累速率增加。在大约1.5×SLB的覆盖率下,随着SLB斑块迅速聚结成连续的SLB,多余的囊泡会解吸。紧接SLB斑块形成之前的可变表面荧光证明存在破裂所需的临界囊泡密度。积累的加速速率和广泛的,突然的囊泡丢失与斑块边缘的出现和消失相吻合。我们得出的结论是,SLB边缘可增强囊泡与表面的粘附力并诱导囊泡破裂,从而在连续SLB的形成中起关键作用。

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