Bordas J, Diakun G P, Diaz F G, Harries J E, Lewis R A, Lowy J, Mant G R, Martin-Fernandez M L, Towns-Andrews E
SERC Daresbury Laboratory, Warrington, UK.
J Muscle Res Cell Motil. 1993 Jun;14(3):311-24. doi: 10.1007/BF00123096.
Results were obtained from contracting frog muscles by collecting high quality time-resolved, two-dimensional, X-ray diffraction patterns at the British Synchrotron Radiation Source (SERC, Daresbury, Laboratory). The structural transitions associated with isometric tension generation were recorded under conditions in which the three-dimensional order characteristic of the rest state is either present or absent. In both cases, new layer lines appear during tension generation, subsequent to changes from activation events in the thin filaments. Compared with the 'decorated' actin layer lines of the rigor state, the spacings of the new layer lines are similar whereas their intensities differ substantially. We conclude that in contracting muscle an actomyosin complex is formed whose structure is not like that in rigor, although it is possible that the interacting sites are the same. Transition from rest to plateau of tension is accompanied by approximately 1.6% increase in the axial spacing of the myosin layer lines. This is explained as arising from axial disposition of the interacting myosin heads in the actomyosin complex. Model calculations are presented which support this view. We argue that in a situation where an actomyosin complex is formed during contraction, one cannot describe the diffraction features as being either thick or thin filament based. Accordingly, the layer lines seen during tension generation are referred to as actomyosin layer lines. It is shown that these layer lines can be indexed as submultiples of a minimum axial repeat of approximately 218.7 nm. After lattice disorder effects are taken into account, the intensity increases on the 15th and 21st AM layer lines at spacings of approximately 14.58 and 10.4 nm respectively, show the same time course as tension rise. However, the time course of the intensity increase of the other actomyosin layer lines and of the spacing change (which is the same for both phenomena) shows a substantial lead over tension rise. These findings suggest that the actomyosin complex formed prior to tension rise is a non-tension-generating state and that this is followed by a transition of the complex to a tension-generating state. The intensity increase in the 15th actomyosin layer line, which parallels tension rise, can be accounted for assuming that in the tension-generating state the attached heads adopt (axially) a more perpendicular orientation with respect to the muscle axis than is seen at rest or in the non-tension-generating state. This suggests the existence of at least two structurally distinct interacting myosin head conformations.(ABSTRACT TRUNCATED AT 400 WORDS)
研究结果是通过在英国同步辐射源(SERC,达累斯伯里实验室)收集高质量的时间分辨二维X射线衍射图,对青蛙肌肉进行收缩实验获得的。在存在或不存在静息态三维有序特征的条件下,记录与等长张力产生相关的结构转变。在这两种情况下,在细丝中激活事件发生变化后,张力产生过程中都会出现新的层线。与僵直状态下“修饰”的肌动蛋白层线相比,新层线的间距相似,但其强度有很大差异。我们得出结论,在收缩的肌肉中形成了一种肌动球蛋白复合物,其结构与僵直状态下的不同,尽管相互作用位点可能相同。从静息到张力平台期的转变伴随着肌球蛋白层线轴向间距增加约1.6%。这被解释为是由于肌动球蛋白复合物中相互作用的肌球蛋白头部的轴向排列所致。给出了支持这一观点的模型计算。我们认为,在收缩过程中形成肌动球蛋白复合物的情况下,不能将衍射特征描述为基于粗丝或细丝的。因此,在张力产生过程中看到的层线被称为肌动球蛋白层线。结果表明,这些层线可以被索引为大约218.7 nm的最小轴向重复的约数。考虑到晶格无序效应后,在间距分别约为14.58和10.4 nm的第15和第21条肌动球蛋白层线上强度增加,与张力上升显示出相同的时间进程。然而,其他肌动球蛋白层线强度增加的时间进程以及间距变化(这两种现象相同)显示出比张力上升有显著的领先。这些发现表明,在张力上升之前形成的肌动球蛋白复合物是一种不产生张力的状态,随后复合物会转变为产生张力的状态。第15条肌动球蛋白层线的强度增加与张力上升平行,可以解释为假设在产生张力的状态下,附着的头部相对于肌肉轴在轴向采用比静息或不产生张力的状态下更垂直的取向。这表明至少存在两种结构上不同的相互作用的肌球蛋白头部构象。(摘要截取自400字)