ADP-induced rocking of the kinesin motor domain revealed by single-molecule fluorescence polarization microscopy

被引:144
作者
Sosa, H
Peterman, EJG
Moerner, WE
Goldstein, LSB
机构
[1] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Howard Hughes Med Inst, La Jolla, CA 92093 USA
[3] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[4] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
基金
美国国家科学基金会;
关键词
D O I
10.1038/88611
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Kinesin is an ATP-driven molecular motor protein that moves processively along microtubules. Despite considerable research, the detailed mechanism of kinesin motion remains elusive. We applied an enhanced suite of single- and multiple-molecule fluorescence polarization microscopy assays to report the orientation and mobility of kinesin molecules bound to microtubules as a function of nucleotide state. In the presence of analogs of ATP, ADP-Pi or in the absence of nucleotide, the kinesin head maintains a rigid orientation. In the presence of ADP, the motor domain of kinesin, still bound to the microtubule, adopts a previously undescribed, highly mobile state. This state may be general to the chemomechanical cycle of motor proteins; in the case of kinesin, the transition from a highly mobile to a rigid state after ADP release may contribute to the generation of the 8 nm step.
引用
收藏
页码:540 / 544
页数:5
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