Geeves M A, Goody R S, Gutfreund H
J Muscle Res Cell Motil. 1984 Aug;5(4):351-61. doi: 10.1007/BF00818255.
Recent experiments on the kinetics of the interaction between myosin subfragment 1 (S1) and F-actin in solution are summarized. It is concluded that, at every step of the ATPase cycle, the association between the two proteins takes place in two stages. The equilibrium constant of the second step and thus the affinity of S1 for actin changes from step to step during the enzymatic reaction. It is proposed that the transient kinetic evidence can be interpreted in terms of two different classes of contraction models. The first one, which is widely used at present, identifies particular steps in the enzymatic reaction as directly responsible for the conformational change which represents the power stroke of muscle contraction (direct coupling model). In the second class of model, to which we wish to draw attention, changes in affinity modulated by the enzymatic reaction result in changes in the relative amounts of time spent by parts of the myosin molecule in two different environments. These environments determine whether the molecule exists in the 'long' or 'short' state, and it is the transition between these two which constitutes the power stroke (indirect coupling model).
本文总结了近期关于溶液中肌球蛋白亚片段1(S1)与F-肌动蛋白相互作用动力学的实验。得出的结论是,在ATP酶循环的每一步,这两种蛋白质之间的结合分两个阶段进行。在酶促反应过程中,第二步的平衡常数以及S1对肌动蛋白的亲和力会逐步骤发生变化。有人提出,瞬态动力学证据可以用两种不同类型的收缩模型来解释。第一种模型目前被广泛使用,它将酶促反应中的特定步骤直接认定为导致代表肌肉收缩动力冲程的构象变化的原因(直接偶联模型)。在我们希望引起关注的第二类模型中,由酶促反应调节的亲和力变化会导致肌球蛋白分子的不同部分在两种不同环境中所花费时间的相对量发生变化。这些环境决定了分子是处于“长”状态还是“短”状态,而这两种状态之间的转变构成了动力冲程(间接偶联模型)。