全内反射荧光显微镜单囊泡成像揭示α -突触核蛋白引起的脂类依赖囊泡聚集。

Chinta Mani Aryal, Owen Tyoe, Jiajie Diao
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引用次数: 4

摘要

单分子方法已被应用于研究纳米尺度上发生的许多生物物理系统的机制。探究囊泡对接、系留、融合、运输、蛋白-膜相互作用等系统的动力学,获得可重复的实验数据;适当的方法和框架至关重要。在这里,我们通过开发一种由合成脂质组成的囊泡固定和使用全内反射荧光(TIRF)显微镜测量的方案来解决这一需求。此外,我们通过使用TIRF显微镜展示了包括由α -突触核蛋白(αSyn)等蛋白质介导的囊泡聚集和外部离子的影响在内的应用。此外,我们利用该方法量化了脂质组成和电荷对αSyn介导的囊泡聚集的依赖,这是基于先前报道的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Lipid Species Dependent Vesicles Clustering Caused by alpha-Synuclein as Revealed by Single-Vesicle Imaging with Total Internal Reflection Fluorescence Microscopy.

Single-molecule methods have been applied to study the mechanisms of many bio-physical systems that occur on the nanometer scale. To probe the dynamics of the such systems including vesicle docking, tethering, fusion, trafficking, protein-membrane interactions, etc., and to obtain reproducible experimental data; proper methodology and framework are crucial. Here, we address this need by developing a protocol for immobilization of vesicles composed of synthetic lipids and measurement using total internal reflection fluorescence (TIRF) microscopy. Furthermore, we demonstrate applications including vesicle clustering mediated by proteins such as alpha-Synuclein (αSyn) and the influence of external ions by using TIRF microscopy. Moreover, we use this method to quantify the dependence of lipid composition and charge on vesicle clustering mediated by αSyn which is based on the methods previously reported.

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CiteScore
1.30
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0.00%
发文量
117
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