Myosin V is a biological Brownian machine.

Biophysics (Nagoya-shi, Japan) Pub Date : 2014-11-01 eCollection Date: 2014-01-01 DOI:10.2142/biophysics.10.69
Keisuke Fujita, Mitsuhiro Iwaki
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Abstract

Myosin V is a vesicle transporter that unidirectionally walks along cytoskeletal actin filaments by converting the chemical energy of ATP into mechanical work. Recently, it was found that myosin V force generation is a composition of two processes: a lever-arm swing, which involves a conformational change in the myosin molecule, and a Brownian search-and-catch, which involves a diffusive "search" by the motor domain that is followed by an asymmetric "catch" in the forward actin target such that Brownian motion is rectified. Here we developed a system that combines optical tweezers with DNA nano-material to show that the Brownian search-and-catch mechanism is the energetically dominant process at near stall force, providing 13 kBT of work compared to just 3 kBT by the lever-arm swing. Our result significantly reconsiders the lever-arm swinging model, which assumes the swing dominantly produces work (>10 kBT), and sheds light on the Brownian search-and-catch as a driving process.

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肌凝蛋白V是一种生物布朗机器。
肌凝蛋白V是一种囊泡转运蛋白,通过将ATP的化学能转化为机械能,单向地沿着细胞骨架肌动蛋白丝行走。最近,人们发现肌凝蛋白V力的产生是由两个过程组成的:杠杆臂摆动,涉及肌凝蛋白分子的构象变化;布朗搜索和捕获,涉及运动域的扩散“搜索”,随后是向前肌动蛋白靶点的不对称“捕获”,从而纠正布朗运动。在这里,我们开发了一个结合光学镊子和DNA纳米材料的系统,以显示布朗搜索和捕获机制是在接近失速力时的能量主导过程,提供13 kBT的功,而杠杆臂摆动仅提供3 kBT的功。我们的结果显著地重新考虑了杠杆臂摆动模型,该模型假设摆动主要产生功(>10 kBT),并阐明了布朗搜索和捕获作为驱动过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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