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(Un)Confined Diffusion of CD59 in the Plasma Membrane Determined by High-Resolution Single Molecule Microscopy

机译:高分辨率单分子显微镜测定CD59在血浆膜中的(无)受限扩散

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摘要

There has been emerging interest whether plasma membrane constituents are moving according to free Brownian motion or hop diffusion. In the latter model, lipids, lipid-anchored proteins, and transmembrane proteins would be transiently confined to periodic corrals in the cell membrane, which are structured by the underlying membrane skeleton. Because this model is based exclusively on results provided by one experimental strategy—high-resolution single particle tracking—we attempted in this study to confirm or amend it using a complementary technique. We developed a novel strategy that employs single molecule fluorescence microscopy to detect confinements to free diffusion of CD59—a GPI-anchored protein—in the plasma membrane of living T24 (ECV) cells. With this method, minimum invasive labeling via fluorescent Fab fragments was sufficient to measure the lateral motion of individual protein molecules on a millisecond timescale, yielding a positional accuracy down to 22 nm. Although no hop diffusion was directly observable, based on a full analytical description our results provide upper boundaries for confinement size and strength.
机译:质膜成分是根据自由布朗运动还是跳跃扩散运动,已经引起了人们的兴趣。在后一种模型中,脂质,脂质锚定蛋白和跨膜蛋白将被瞬时限制在细胞膜中的周期性皮质中,后者由下面的膜骨架构成。由于此模型仅基于一种实验策略(高分辨率单粒子跟踪)提供的结果,因此我们在本研究中尝试使用补充技术来确认或修正它。我们开发了一种新的策略,该策略采用单分子荧光显微镜技术检测活体T24(ECV)细胞质膜中CD59(一种GPI固定蛋白)的自由扩散限制。使用这种方法,通过荧光Fab片段进行的最小侵入性标记足以在毫秒级的时间尺度上测量单个蛋白质分子的横向运动,从而产生低至22 nm的位置精度。尽管没有直接观察到跃点扩散,但基于完整的分析说明,我们的结果为限制尺寸和强度提供了上限。

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