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单货物纳米分辨率追踪揭示动力蛋白运动机制。

Nanometer-resolution tracking of single cargo reveals dynein motor mechanisms.

作者信息

Peng Chunte Sam, Zhang Yunxiang, Liu Qian, Marti G Edward, Huang Yu-Wen Alvin, Südhof Thomas C, Cui Bianxiao, Chu Steven

机构信息

Department of Physics, Stanford University, Stanford, CA, USA.

Department of Molecular and Cellular Physiology, Stanford University, Stanford, CA, USA.

出版信息

Nat Chem Biol. 2025 May;21(5):648-656. doi: 10.1038/s41589-024-01694-2. Epub 2024 Aug 1.

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.

摘要

胞质动力蛋白对于细胞内运输至关重要。尽管在体外进行了广泛的表征,但动力蛋白马达如何在活细胞中通过连续步骤运输囊泡仍不清楚。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粒子追踪。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在一到五个动力蛋白马达之间随机切换。我们非常明亮的光学探针允许观察单个分子步骤。引人注目的是,这些测量结果表明,步骤之间的停留时间由两个温度依赖性速率常数控制,其中在每个动力蛋白步骤中依次水解两个ATP分子。因此,我们的观察结果揭示了活细胞中动力蛋白介导的货物运输之前未知的化学机械循环。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b26/12037413/0bf955637b40/41589_2024_1694_Fig1_HTML.jpg

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