Brenner B, Eisenberg E
Proc Natl Acad Sci U S A. 1986 May;83(10):3542-6. doi: 10.1073/pnas.83.10.3542.
Crossbridge models of muscle contraction based on biochemical studies predict that there may be a relationship between the rate-limiting step in the actomyosin ATPase cycle in vitro and the rate of force development in vivo. In the present study, we measured the rate of force redevelopment in skinned rabbit muscle fibers following unloaded isotonic shortening and a rapid restretch. For comparison, ATPase activity was measured under identical conditions, using myosin subfragment-1 chemically crosslinked to actin. We found that the time course of force redevelopment is well fitted by a single exponential function, implying that force redevelopment is a first-order process, described by a single rate constant. The magnitude of this rate constant is in close agreement with the rate constant necessary to simulate the experimental force-velocity relation on the basis of a crossbridge model of the type proposed by A. F. Huxley in 1957. In addition, the observed close correlation between the rate constant for force redevelopment and the maximal actin-activated actomyosin ATPase rate under a variety of conditions suggests that the step that determines the rate of force generation in the crossbridge cycle may be the physiological equivalent of the rate-limiting step in the actomyosin ATPase cycle in solution.
基于生化研究的肌肉收缩横桥模型预测,体外肌动球蛋白ATP酶循环中的限速步骤与体内力量发展速率之间可能存在关联。在本研究中,我们测量了去表皮兔肌纤维在无负荷等张收缩和快速再拉伸后的力量重新发展速率。为作比较,在相同条件下,使用化学交联到肌动蛋白的肌球蛋白亚片段-1测量ATP酶活性。我们发现力量重新发展的时间进程能很好地用单一指数函数拟合,这意味着力量重新发展是一个一级过程,由单一速率常数描述。该速率常数的大小与基于A.F.赫胥黎1957年提出的那种横桥模型来模拟实验性力量-速度关系所需的速率常数密切一致。此外,在各种条件下观察到的力量重新发展速率常数与最大肌动蛋白激活的肌动球蛋白ATP酶速率之间的紧密相关性表明,在横桥循环中决定力量产生速率的步骤可能在生理上等同于溶液中肌动球蛋白ATP酶循环的限速步骤。