肌肉收缩的机制。

R Cooke
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引用次数: 269

摘要

从对溶液中肌动蛋白和肌球蛋白相互作用的研究,从对肌纤维结构的阐明,以及从纤维收缩的力学和能量学的测量中获得了收缩机制的知识。肌动蛋白和肌凝蛋白亚片段在溶液中水解ATP,已经建立了许多状态和它们之间的过渡速率。一个主要的目标是现在了解这种相互作用的动力学是如何改变的,当它发生在肌原纤维的组织阵列。早期对肌肉结构的研究表明,肌球蛋白交叉桥方向的改变是产生力的原因。最近,连接在交叉桥上的荧光和顺磁探针表明,至少交叉桥的一些结构域在力产生过程中不会改变方向。通过测量纤维的稳态收缩和纤维长度或张力阶跃变化后的瞬态,可以确定有源交叉桥的许多特性。综上所述,这些研究提供了确凿的证据,证明力是由一个循环相互作用产生的,在这个循环相互作用中,肌凝蛋白交叉桥附着在肌动蛋白上,通过12纳米的“强力冲程”施加力,然后通过ATP的结合释放。这种相互作用在分子水平上的机制尚不清楚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The mechanism of muscle contraction.

Knowledge of the mechanism of contraction has been obtained from studies of the interaction of actin and myosin in solution, from an elucidation of the structure of muscle fibers, and from measurements of the mechanics and energetics of fiber contraction. Many of the states and the transition rates between them have been established for the hydrolysis of ATP by actin and myosin subfragments in solution. A major goal is to now understand how the kinetics of this interaction are altered when it occurs in the organized array of the myofibril. Early work on the structure of muscle suggested that changes in the orientation of myosin cross-bridges were responsible for the generation of force. More recently, fluorescent and paramagnetic probes attached to the cross-bridges have suggested that at least some domains of the cross-bridges do not change orientation during force generation. A number of properties of active cross-bridges have been defined by measurements of steady state contractions of fibers and by the transients which follow step changes in fiber length or tension. Taken together these studies have provided firm evidence that force is generated by a cyclic interaction in which a myosin cross-bridge attaches to actin, exerts force through a "powerstroke" of 12 nm, and is then released by the binding of ATP. The mechanism of this interaction at the molecular level remains unknown.

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