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用沉淀染料在活细胞中记录的驱动蛋白-1 活性。

Kinesin-1 activity recorded in living cells with a precipitating dye.

机构信息

School of Chemistry and Biochemistry, NCCR Chemical Biology, Faculty of Science, University of Geneva, Geneva, Switzerland.

Department of Cell Biology, Faculty of Science, University of Geneva, Geneva, Switzerland.

出版信息

Nat Commun. 2021 Mar 5;12(1):1463. doi: 10.1038/s41467-021-21626-1.

Abstract

Kinesin-1 is a processive motor protein that uses ATP-derived energy to transport a variety of intracellular cargoes toward the cell periphery. The ability to visualize and monitor kinesin transport in live cells is critical to study the myriad of functions associated with cargo trafficking. Herein we report the discovery of a fluorogenic small molecule substrate (QPD-OTf) for kinesin-1 that yields a precipitating dye along its walking path on microtubules (MTs). QPD-OTf enables to monitor native kinesin-1 transport activity in cellulo without external modifications. In vitro assays show that kinesin-1 and MTs are sufficient to yield fluorescent crystals; in cells, kinesin-1 specific transport of cargo from the Golgi appears as trails of fluorescence over time. These findings are further supported by docking studies, which suggest the binding of the activity-based substrate in the nucleotide binding site of kinesin-1.

摘要

驱动蛋白-1 是一种进行性马达蛋白,它利用 ATP 衍生的能量将各种细胞内货物运输到细胞外周。在活细胞中可视化和监测驱动蛋白运输的能力对于研究与货物运输相关的众多功能至关重要。在此,我们报告了一种用于驱动蛋白-1 的荧光小分子底物 (QPD-OTf) 的发现,该底物在微管 (MTs) 上沿其行走路径产生沉淀染料。QPD-OTf 可在不进行外部修饰的情况下在细胞内监测天然驱动蛋白-1 的运输活性。体外实验表明,驱动蛋白-1 和 MTs 足以产生荧光晶体;在细胞中,高尔基体内货物的驱动蛋白-1 特异性运输随着时间的推移表现为荧光轨迹。这些发现进一步得到对接研究的支持,该研究表明活性基底物与驱动蛋白-1 的核苷酸结合位点结合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90fa/7935933/44ccbe097eda/41467_2021_21626_Fig1_HTML.jpg

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