对单个货物的纳米分辨率追踪揭示了动力蛋白的运动机制。

IF 12.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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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来源期刊
Nature chemical biology
Nature chemical biology 生物-生化与分子生物学
CiteScore
23.90
自引率
1.40%
发文量
238
审稿时长
12 months
期刊介绍: Nature Chemical Biology stands as an esteemed international monthly journal, offering a prominent platform for the chemical biology community to showcase top-tier original research and commentary. Operating at the crossroads of chemistry, biology, and related disciplines, chemical biology utilizes scientific ideas and approaches to comprehend and manipulate biological systems with molecular precision. The journal embraces contributions from the growing community of chemical biologists, encompassing insights from chemists applying principles and tools to biological inquiries and biologists striving to comprehend and control molecular-level biological processes. We prioritize studies unveiling significant conceptual or practical advancements in areas where chemistry and biology intersect, emphasizing basic research, especially those reporting novel chemical or biological tools and offering profound molecular-level insights into underlying biological mechanisms. Nature Chemical Biology also welcomes manuscripts describing applied molecular studies at the chemistry-biology interface due to the broad utility of chemical biology approaches in manipulating or engineering biological systems. Irrespective of scientific focus, we actively seek submissions that creatively blend chemistry and biology, particularly those providing substantial conceptual or methodological breakthroughs with the potential to open innovative research avenues. The journal maintains a robust and impartial review process, emphasizing thorough chemical and biological characterization.
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