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

被引:22
作者
Angerani, Simona [1 ]
Lindberg, Eric [1 ]
Klena, Nikolai [2 ]
Bleck, Christopher K. E. [3 ]
Aumeier, Charlotte [1 ]
Winssinger, Nicolas [1 ]
机构
[1] Univ Geneva, Fac Sci, Sch Chem & Biochem, NCCR Chem Biol, Geneva, Switzerland
[2] Univ Geneva, Fac Sci, Dept Cell Biol, Geneva, Switzerland
[3] NHLBI, Elect Microscopy Core Facil, NIH, Bethesda, MD USA
关键词
GOLGI-COMPLEX; MOTOR PROTEIN; BREFELDIN-A; MICROTUBULES; MOTILITY; ER; PROCESSIVITY; MOLECULES; SUBSTRATE; BINDING;
D O I
10.1038/s41467-021-21626-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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. Monitoring the activity of the processive motor protein kinesin-1 in live cells is currently difficult. Here the authors report the fluorogenic small molecule QPD-OTf, a kinesin-1 substrate that causes activity-dependent dye precipitation.
引用
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页数:10
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