动力蛋白
动态素
分子马达
细胞生物学
运动蛋白
生物物理学
ATP水解
生物
驱动蛋白
微管
化学
生物化学
酶
ATP酶
作者
Chunte Sam Peng,Yunxiang Zhang,Qian Liu,G. Edward Marti,Yu‐Wen Alvin Huang,Thomas C. Südhof,Bianxiao Cui,Steven Chu
标识
DOI:10.1038/s41589-024-01694-2
摘要
Abstract Cytoplasmic dynein is essential for intracellular transport. Despite extensive in vitro characterizations, how the dynein motors transport vesicles by processive steps in live cells remains unclear. To dissect the molecular mechanisms of dynein, we develop optical probes that enable long-term single-particle tracking in live cells with high spatiotemporal resolution. We find that the number of active dynein motors transporting cargo switches stochastically between one and five dynein motors during long-range transport in neuronal axons. Our very bright optical probes allow the observation of individual molecular steps. Strikingly, these measurements reveal that the dwell times between steps are controlled by two temperature-dependent rate constants in which two ATP molecules are hydrolyzed sequentially during each dynein step. Thus, our observations uncover a previously unknown chemomechanical cycle of dynein-mediated cargo transport in living cells.
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