Single-molecule live-cell imaging of clathrin-based endocytosis.

Tomas Kirchhausen, Werner Boll, Antoine van Oijen, Marcelo Ehrlich
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引用次数: 16

Abstract

Clathrin-coated vesicles carry traffic from the plasma membrane to endosomes. We report here the first real-time visualization of cargo sorting and endocytosis by clathrin-coated pits in living cells. We have visualized the formation of coats by monitoring the incorporation of fluorescently tagged clathrin or its adaptor AP-2 (adaptor protein 2), and have followed clathrin-mediated uptake of transferrin, single LDL (low-density lipoprotein) and single reovirus particles. The intensity of a cargo-loaded clathrin cluster grows steadily during its lifetime, and the time required to complete assembly is proportional to the size of the cargo particle. These results are consistent with a nucleation-growth mechanism and an approximately constant growth rate. There are no preferred nucleation sites. A proportion of the nucleation events appear to be abortive. Cargo incorporation occurs primarily or exclusively in a newly formed coated pit, and loading appears to commit that pit to finish assembly. Our data led to a model in which coated pits initiate randomly, but collapse with high likelihood unless stabilized, presumably by cargo capture.

基于网格蛋白内吞作用的单分子活细胞成像。
包覆网格蛋白的囊泡将交通从质膜运送到核内体。我们在这里报告了第一个实时可视化的货物分类和内吞作用由网格蛋白包裹的坑活细胞。我们通过监测荧光标记的网格蛋白或其接头AP-2(接头蛋白2)的结合,可视化了外壳的形成,并跟踪了网格蛋白介导的转铁蛋白、单LDL(低密度脂蛋白)和单呼肠孤病毒颗粒的摄取。装载货物的网格蛋白簇的强度在其生命周期中稳定增长,完成组装所需的时间与货物颗粒的大小成正比。这些结果符合成核生长机制和近似恒定的生长速率。没有优先的成核位置。有一部分成核事件似乎是流产的。货物合并主要或完全发生在新形成的涂层坑中,装载似乎使该坑完成组装。我们的数据导致了一个模型,其中涂覆坑随机启动,但坍塌的可能性很高,除非稳定,大概是由货物捕获。
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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