Yu L C, Arata T, Steven A C, Naylor G R, Gamble R C, Podolsky R J
Adv Exp Med Biol. 1984;170:207-20. doi: 10.1007/978-1-4684-4703-3_19.
Structural studies concerned with force generating mechanisms in striated muscle fibers in different states are described. The first study deals with fibers in the "rigor" state, where ATP is absent and all the myosin heads form cross-bridges with the actin-containing filaments. In this state large axial forces are developed when ionic strength is reduced to very low levels. At the same time, the fiber expands radially, as indicated by both X-ray diffraction and light microscopy. Comparison of the latter two measurements indicates that force is developed in part because of differences in the lateral expandability of different parts of the sarcomere. Thus, under these conditions, force appears to be modulated by factors that operate at the filament rather than the cross-bridge level. The second study deals with the location of the myosin heads in the relaxed state, and the mass movement that takes place when the fiber is physiologically activated. By using the intense X-ray source at the Stanford Synchrotron Radiation Laboratory, five equatorial reflections were recorded for both the relaxed and the activated state, and a spatial resolution of 100 A was obtained. Analysis of the data indicates that (1) in the resting state, myosin heads protrude out from the thick filaments and extend toward the thin filaments, and (2) upon activation, significant loss of mass occurs only in the region peripheral to the thick filament backbone through a movement that has a pronounced azimuthal component. The latter movement can be taken as the overall shift in myosin subfragment 1 during the cross-bridge cycle.
本文描述了关于不同状态下横纹肌纤维力产生机制的结构研究。第一项研究涉及处于“僵直”状态的纤维,此时不存在ATP,所有肌球蛋白头部与含肌动蛋白的细丝形成横桥。在这种状态下,当离子强度降低到非常低的水平时会产生较大的轴向力。同时,如X射线衍射和光学显微镜所示,纤维会径向扩张。后两种测量方法的比较表明,产生力的部分原因是肌节不同部分横向可扩展性的差异。因此,在这些条件下,力似乎是由在细丝而非横桥水平起作用的因素调节的。第二项研究涉及肌球蛋白头部在松弛状态下的位置,以及纤维在生理激活时发生的质量移动。通过使用斯坦福同步辐射实验室的强X射线源,记录了松弛状态和激活状态下的五个赤道反射,并获得了100埃的空间分辨率。数据分析表明:(1)在静止状态下,肌球蛋白头部从粗丝中伸出并向细丝延伸;(2)激活后,只有在粗丝主干外围区域通过具有明显方位角分量的移动才会发生明显的质量损失。后一种移动可被视为横桥循环期间肌球蛋白亚片段1的整体移动。