Hill T L, Eisenberg E, Greene L E
Proc Natl Acad Sci U S A. 1983 Jan;80(1):60-4. doi: 10.1073/pnas.80.1.60.
In this paper we introduce an alternate model for the equilibrium binding of S-l-N (S-l, subfragment l of myosin; N, nucleotide) on the troponin-tropomyosin-actin complex, including the influence of Ca2+ on this binding. In our previous model [Hill, T. L., Eisenberg, E. & Greene, L. E. (1980) Proc. Natl. Acad. Sci. USA 77, 3186-3190], we assumed that each tropomyosin unit, including one troponin-tropomyosin molecule and seven actin sites on the actin filament, could exist in two conformational states which presumably differed in the position of the tropomyosin on the actin. The binding of S-l-N or Ca2+ to the tropomyosin unit shifted the equilibrium between the two states but did not affect the intrinsic conformation of each state. In contrast, in the present model, we assume that tropomyosin can in principle occupy a continuum of positions on the actin filament. However, in any particular circumstance (N, Ca2+, salt, temperature), the tropomyosin occupies only a single position rather than existing in a dynamic equilibrium between two positions as in our earlier model. The binding of S-l-N or Ca2+ changes the position of tropomyosin on the actin filament and the exact position that the tropomyosin occupies depends on the nucleotide bound to S-l.
在本文中,我们介绍了一种关于S-1-N(S-1,肌球蛋白亚片段1;N,核苷酸)在肌钙蛋白-原肌球蛋白-肌动蛋白复合物上平衡结合的替代模型,包括Ca2+对这种结合的影响。在我们之前的模型[希尔,T.L.,艾森伯格,E.和格林,L.E.(1980年)《美国国家科学院院刊》77,3186 - 3190]中,我们假设每个原肌球蛋白单元,包括一个肌钙蛋白-原肌球蛋白分子和肌动蛋白丝上的七个肌动蛋白位点,可存在于两种构象状态,这两种状态可能在原肌球蛋白在肌动蛋白上的位置有所不同。S-1-N或Ca2+与原肌球蛋白单元的结合会改变这两种状态之间的平衡,但不影响每种状态的固有构象。相比之下,在当前模型中,我们假设原肌球蛋白原则上可占据肌动蛋白丝上的一系列连续位置。然而,在任何特定情况下(N、Ca2+、盐、温度),原肌球蛋白仅占据单一位置,而不像我们早期模型那样存在于两个位置之间的动态平衡中。S-1-N或Ca2+的结合会改变原肌球蛋白在肌动蛋白丝上的位置,并且原肌球蛋白占据的确切位置取决于与S-1结合的核苷酸。