驱动蛋白
微管
三磷酸腺苷
生物物理学
ATP水解
化学
运动蛋白
分子马达
二聚体
生物
细胞生物学
生物化学
ATP酶
有机化学
酶
作者
Ahmet Yıldız,Michio Tomishige,Ronald D. Vale,Paul R. Selvin
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2003-12-23
卷期号:303 (5658): 676-678
被引量:939
标识
DOI:10.1126/science.1093753
摘要
Kinesin is a processive motor that takes 8.3-nm center-of-mass steps along microtubules for each adenosine triphosphate hydrolyzed. Whether kinesin moves by a “hand-over-hand” or an “inchworm” model has been controversial. We have labeled a single head of the kinesin dimer with a Cy3 fluorophore and localized the position of the dye to within 2 nm before and after a step. We observed that single kinesin heads take steps of 17.3 ± 3.3 nm. A kinetic analysis of the dwell times between steps shows that the 17-nm steps alternate with 0-nm steps. These results strongly support a hand-over-hand mechanism, and not an inchworm mechanism. In addition, our results suggest that kinesin is bound by both heads to the microtubule while it waits for adenosine triphosphate in between steps.
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