Chunte Sam Peng, Yunxiang Zhang, Qian Liu, G Edward Marti, Yu-Wen Alvin Huang, Thomas C Südhof, Bianxiao Cui, Steven Chu
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引用次数: 0
摘要
细胞质动力蛋白对细胞内运输至关重要。尽管进行了广泛的体外表征,但仍不清楚肌球蛋白马达如何在活细胞中通过过程步骤运输囊泡。为了剖析动力蛋白的分子机制,我们开发了光学探针,能够在活细胞中以高时空分辨率进行长期单颗粒跟踪。我们发现,在神经元轴突的长距离运输过程中,运输货物的活性动力蛋白马达数量会在一个到五个动力蛋白马达之间随机切换。我们的高亮度光学探针可以观察到各个分子步骤。令人震惊的是,这些测量结果表明,各步骤之间的停留时间受两个与温度相关的速率常数控制,在每个动力蛋白步骤中,两个 ATP 分子依次水解。因此,我们的观察结果揭示了活细胞中由动力蛋白介导的货物运输的化学机械循环。
Nanometer-resolution tracking of single cargo reveals dynein motor mechanisms.
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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