Kikkawa M, Sablin E P, Okada Y, Yajima H, Fletterick R J, Hirokawa N
Department of Cell Biology and Anatomy, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo Bunkyo-ku, Tokyo 113-0033, Japan.
Nature. 2001 May 24;411(6836):439-45. doi: 10.1038/35078000.
Kinesin motors are specialized enzymes that use hydrolysis of ATP to generate force and movement along their cellular tracks, the microtubules. Although numerous biochemical and biophysical studies have accumulated much data that link microtubule-assisted ATP hydrolysis to kinesin motion, the structural view of kinesin movement remains unclear. This study of the monomeric kinesin motor KIF1A combines X-ray crystallography and cryo-electron microscopy, and allows analysis of force-generating conformational changes at atomic resolution. The motor is revealed in its two functionally critical states-complexed with ADP and with a non-hydrolysable analogue of ATP. The conformational change observed between the ADP-bound and the ATP-like structures of the KIF1A catalytic core is modular, extends to all kinesins and is similar to the conformational change used by myosin motors and G proteins. Docking of the ADP-bound and ATP-like crystallographic models of KIF1A into the corresponding cryo-electron microscopy maps suggests a rationale for the plus-end directional bias associated with the kinesin catalytic core.
驱动蛋白是一类特殊的酶,它们利用ATP水解产生沿细胞轨道微管移动的力。尽管大量的生物化学和生物物理学研究积累了许多将微管辅助ATP水解与驱动蛋白运动联系起来的数据,但驱动蛋白运动的结构观点仍不明确。这项对单体驱动蛋白KIF1A的研究结合了X射线晶体学和冷冻电子显微镜技术,并能够在原子分辨率下分析产生力的构象变化。该驱动蛋白呈现出两种功能关键状态——与ADP结合以及与ATP的不可水解类似物结合。在KIF1A催化核心的ADP结合结构和ATP样结构之间观察到的构象变化是模块化的,延伸至所有驱动蛋白,并且类似于肌球蛋白和G蛋白所使用的构象变化。将KIF1A的ADP结合和ATP样晶体学模型对接至相应的冷冻电子显微镜图谱中,为与驱动蛋白催化核心相关的正端方向偏好提供了一种解释。