Brenner B, Yu L C, Greene L E, Eisenberg E, Schoenberg M
Biophys J. 1986 Dec;50(6):1101-8. doi: 10.1016/S0006-3495(86)83554-8.
We find that at 6 degrees C in the presence of 4 mM MgPPi, at low or moderate ionic strength, skinned rabbit psoas fibers exhibit a stiffness and an equatorial x-ray diffraction pattern similar to that of rigor fibers. As the ionic strength is increased in the absence of Ca2+, both the stiffness and the equatorial x-ray diffraction pattern approach those of the relaxed state. This suggests that, as in solution, increasing ionic strength weakens the affinity of myosin cross-bridges for actin, which results in a decrease in the number of cross-bridges attached. The effect is Ca2+-sensitive. Assuming that stiffness is a measure of the number of cross-bridge heads attached, in the absence of Ca2+, the fraction of attached cross-bridge heads varies from approximately 75% to approximately 25% over an ionic strength range where ionic strength in solution weakens the binding constant for myosin subfragment-1 binding to unregulated actin by less than a factor of 3. Therefore, this phenomenon appears similar to the cooperative Ca2+-sensitive binding of S1 to regulated actin in solution (Greene, L. E., and E. Eisenberg, 1980, Proc. Natl. Acad. Sci. USA, 77:2616). By comparing the binding constants in solution and in the fiber under similar conditions, we find that the "effective actin concentration," that is, the concentration that gives the same fraction of S1 molecules bound to actin in solution as cross-bridge heads are bound to actin in a fiber, is in the millimolar range. An effective actin concentration in the millimolar range suggests that the strength of actin binding to cross-bridges in fibers may be several orders of magnitude weaker than the strength of ATP binding. Previously, it has been assumed that these two quantities were equal, as this gives the minimum energy loss when ATP dissociates the cross-bridge from actin (Morales, 1980, J. Supramol. Struct., 3:105:1975; Eisenberg, E.,Hill, T. L. and Y. Chen, 1980, Biophys. J., 29:195).
我们发现,在4 mM 焦磷酸镁存在的情况下,于6摄氏度、低或中等离子强度条件下,去膜的兔腰大肌纤维表现出与僵直纤维相似的硬度和赤道X射线衍射图样。在无Ca2+ 时随着离子强度增加,硬度和赤道X射线衍射图样均趋近于松弛状态。这表明,如同在溶液中一样,增加离子强度会减弱肌球蛋白横桥与肌动蛋白的亲和力,导致附着的横桥数量减少。该效应是对Ca2+ 敏感的。假设硬度是附着的横桥头数量的一种度量,在无Ca2+ 时,在溶液中离子强度使肌球蛋白亚片段-1与未调节的肌动蛋白结合的结合常数减弱不到3倍的离子强度范围内,附着的横桥头比例从约75%变化到约25%。因此,这种现象似乎类似于溶液中S1与调节的肌动蛋白的协同Ca2+ 敏感结合(格林,L.E.,和E.艾森伯格,1980年,《美国国家科学院院刊》,77:2616)。通过比较相似条件下溶液中和纤维中的结合常数,我们发现,“有效肌动蛋白浓度”,即溶液中使结合到肌动蛋白的S1分子比例与纤维中横桥头结合到肌动蛋白的比例相同的浓度,处于毫摩尔范围内。毫摩尔范围内的有效肌动蛋白浓度表明,纤维中肌动蛋白与横桥的结合强度可能比ATP结合强度弱几个数量级。以前曾假定这两个量是相等的,因为这在ATP使横桥从肌动蛋白上解离时给出最小的能量损失(莫拉莱斯,1980年,《超分子结构杂志》,3:105:1975;艾森伯格,E.,希尔,T.L.和Y.陈,1980年,《生物物理学杂志》,29:195)。