Myosin V and Kinesin act as tethers to enhance each others' processivity

被引:104
作者
Ali, M. Yusuf [1 ]
Lu, Hailong [1 ]
Bookwalter, Carol S. [1 ]
Warshaw, David M. [1 ]
Trybus, Kathleen M. [1 ]
机构
[1] Univ Vermont, Dept Mol Physiol & Biophys, Burlington, VT 05405 USA
关键词
actin; microtubule; molecular motor; Qdot; electrostatic;
D O I
10.1073/pnas.0711531105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Organelle transport to the periphery of the cell involves coordinated transport between the processive motors kinesin and myosin V. Long-range transport takes place on microtubule tracks, whereas final delivery involves shorter actin-based movements. The concept that motors only function on their appropriate track required further investigation with the recent observation that myosin V undergoes a diffusional search on microtubules. Here we show, using single-molecule techniques, that a functional consequence of myosin V's diffusion on microtubules is a significant enhancement of the processive run length of kinesin when both motors are present on the same cargo. The degree of run length enhancement correlated with the net positive charge in loop 2 of myosin V. On actin, myosin V also undergoes longer processive runs when kinesin is present on the same cargo. The process that causes run length enhancement on both cytoskeletal tracks is electrostatic. We propose that one motor acts as a tether for the other and prevents its diffusion away from the track, thus allowing more steps to be taken before dissociation. The resulting run length enhancement likely contributes to the successful delivery of cargo in the cell.
引用
收藏
页码:4691 / 4696
页数:6
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