Yildiz Ahmet, Tomishige Michio, Vale Ronald D, Selvin Paul R
Center for Biophysics and Computational Biology, University of Illinois, Urbana-Champaign, IL 61801, USA.
Science. 2004 Jan 30;303(5658):676-8. doi: 10.1126/science.1093753. Epub 2003 Dec 18.
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.
驱动蛋白是一种持续性马达蛋白,每水解一个三磷酸腺苷,它会沿着微管以8.3纳米的质心步长移动。驱动蛋白是通过“手换手”模型还是“尺蠖”模型移动一直存在争议。我们用Cy3荧光团标记了驱动蛋白二聚体的单个头部,并在步移前后将染料的位置定位在2纳米以内。我们观察到单个驱动蛋白头部的步长为17.3±3.3纳米。对步移之间停留时间的动力学分析表明,17纳米的步移与0纳米的步移交替出现。这些结果有力地支持了“手换手”机制,而非“尺蠖”机制。此外,我们的结果表明,驱动蛋白在步移之间等待三磷酸腺苷时,其两个头部都与微管结合。