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肌球蛋白 V 在进行性运动过程中尾部和头部运动的同时观察。

Simultaneous observation of tail and head movements of myosin V during processive motion.

机构信息

Department of Molecular Physiology and Biophysics, University of Vermont, Burlington, Vermont 05405, USA.

出版信息

J Biol Chem. 2010 Dec 31;285(53):42068-74. doi: 10.1074/jbc.M110.180265. Epub 2010 Oct 25.

Abstract

Processive stepping of myosin Va (myoV) has been tracked by monitoring either the tail position (center of mass) or the position of one or both heads. Here, we combine these two approaches by attaching a quantum dot to one of the motor domains and a bead to the tail. Using laser trapping and total internal reflection microscopy, the position of one head and the tail are observed simultaneously as myoV moves processively on an actin filament bundle against the resistive load of the laser trap. The head moves one step (73 ± 10 nm) for every two steps of the tail (35 ± 9 nm). One tail step occurs concurrently with quantum dot-labeled head movement, whereas the other occurs with movement of the unlabeled head, consistent with a hand-over-hand model. Load increases the probability of the motor taking a back step. The back step is triggered by the motor taking a shorter forward step (head step, 68 ± 11 nm; tail step, 32 ± 10 nm), likely one actin monomer short of its preferred binding site. During a back step, the motor reverses its hand-over-hand motion, with the leading head detaching and reattaching to one of multiple actin sites behind the trailing head. After a back step, the motor can correct its mistake and step processively forward at resistive loads <0.7 piconewton or stall or detach at higher loads. Back stepping may provide a mechanism to ensure efficient cargo delivery even when myoV encounters obstacles within the actin cytoskeletal meshwork or when other motors are attached to the same cargo.

摘要

肌球蛋白 Va(myoV)的连续运动已通过监测尾部(质心)或一个或两个头部的位置来跟踪。在这里,我们通过将量子点附着到一个马达结构域上并将珠子附着到尾部上来结合这两种方法。使用激光捕获和全内反射显微镜,当 myoV 在肌动蛋白丝束上移动以抵抗激光捕获的阻力负载时,同时观察一个头部和尾部的位置。头部每移动两个步(35 ± 9nm)就移动一步(73 ± 10nm)。一个尾部步与量子点标记的头部运动同时发生,而另一个尾部步与未标记的头部运动同时发生,与手拉手模型一致。负载增加了马达向后移动的可能性。后向步由马达向前移动的步幅变短(头部步,68 ± 11nm;尾部步,32 ± 10nm)触发,可能是一个肌动蛋白单体短于其首选结合位点。在后向步中,马达反转其手拉手运动,领头头脱离并重新附着在尾随头后面的多个肌动蛋白位点之一上。在后向步之后,马达可以在抵抗负载<0.7 皮牛顿或失速或在更高负载下脱离的情况下,向前连续地移动。向后移动可能提供一种机制,即使在 myoV 遇到肌动蛋白细胞骨架网络内的障碍物或其他马达附着在同一货物上时,也能确保有效货物传递。

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