Torque Generation of Kinesin Motors Is Governed by the Stability of the Neck Domain

被引:63
作者
Brunnbauer, Melanie [1 ]
Dombi, Renate [2 ,3 ]
Ho, Thi-Hieu [2 ,3 ]
Schliwa, Manfred [2 ,3 ]
Rief, Matthias [1 ]
Oekten, Zeynep [1 ,2 ,3 ]
机构
[1] Tech Univ Munich, Phys Dept E22, D-85748 Garching, Germany
[2] Univ Munich, Inst Cell Biol, D-80336 Munich, Germany
[3] Univ Munich, Ctr Integrated Prot Sci Munich, D-80336 Munich, Germany
关键词
END-DIRECTED MOTOR; COILED-COIL; INTRAFLAGELLAR TRANSPORT; HETERODIMER FORMATION; STEPPING BEHAVIOR; MOLECULAR MOTORS; POWER STROKE; IN-VITRO; PROTEIN; MICROTUBULES;
D O I
10.1016/j.molcel.2012.04.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
In long-range transport of cargo, prototypical kinesin-1 steps along a single protofilament on the microtubule, an astonishing behavior given the number of theoretically available binding sites on adjacent protofilaments. Using a laser trap assay, we analyzed the trajectories of several representatives from the kinesin-2 class on freely suspended microtubules. In stark contrast to kinesin-1, these motors display a wide range of left-handed spiraling around microtubules and thus generate torque during cargo transport. We provide direct evidence that kinesin's neck region determines the torque-generating properties. A model system based on kinesin-1 corroborates this result: disrupting the stability of the neck by inserting flexible peptide stretches resulted in pronounced left-handed spiraling. Mimicking neck stability by crosslinking significantly reduced the spiraling of the motor up to the point of protofilament tracking. Finally, we present a model that explains the physical basis of kinesin's spiraling around the microtubule.
引用
收藏
页码:147 / 158
页数:12
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