Luther P K
Blackett Laboratory, Imperial College, London, England.
J Cell Biol. 1991 Jun;113(5):1043-55. doi: 10.1083/jcb.113.5.1043.
The three-dimensional structure of the Z-band in fish white muscle has been investigated by electron microscopy. This Z-band is described as simple, since in longitudinal sections it has the appearance of a single zigzag pattern connecting the ends of actin filaments of opposite polarity from adjacent sarcomeres. The reconstruction shows two pairs of links, the Z-links, between one actin filament and the facing four actin filaments in the adjacent sarcomere. The members of each pair have nearly diametrically opposed origins. In relation to one actin filament, one pair of links appears to bind along the final 10 nm of the actin filament (proximal site) and the other pair binds along a region extending from 5 to 20 nm from the filament end (distal site). Between one pair and the other, there is a rotation of approximately 80 degrees round the filament axis. A Z-link with a proximal site at the end of one actin filament attaches at a distal site on the oppositely oriented actin filaments of the facing sarcomere and vice versa. The length of each Z-link is consistent with the length of an alpha-actinin molecule. An additional set of links located 10-15 nm from the center of the Z-band occurs between actin filaments of the same polarity. These polar links connect the actin filaments along the same direction on each side of the Z-band. The three-dimensional structure appears to have twofold screw symmetry about the central plane of the Z-band. Only approximate twofold rotational symmetry is observed in directions parallel to the actin filaments. Previous models of the Z-band in which four identical and rotationally symmetrical links emanate from the end of one actin filament and span across to the ends of four actin filaments in the adjacent sarcomere are therefore incorrect.
通过电子显微镜对鱼类白肌中Z带的三维结构进行了研究。该Z带被描述为简单的,因为在纵向切片中它呈现出单一的锯齿状图案,连接相邻肌节中相反极性的肌动蛋白丝的末端。重建显示在一条肌动蛋白丝与相邻肌节中相对的四条肌动蛋白丝之间有两对连接,即Z连接。每对连接的成员几乎在直径方向上相对起源。相对于一条肌动蛋白丝,一对连接似乎沿着肌动蛋白丝的最后10纳米(近端位点)结合,另一对连接沿着从丝末端延伸5至20纳米的区域(远端位点)结合。一对连接与另一对连接之间,围绕丝轴有大约80度的旋转。在一条肌动蛋白丝末端具有近端位点的Z连接附着在相对肌节中相反方向的肌动蛋白丝的远端位点上,反之亦然。每个Z连接的长度与α-辅肌动蛋白分子的长度一致。在距离Z带中心10 - 15纳米处还存在一组额外的连接,位于相同极性的肌动蛋白丝之间。这些极性连接沿着Z带两侧相同方向连接肌动蛋白丝。三维结构似乎围绕Z带的中心平面具有二重螺旋对称性。在平行于肌动蛋白丝的方向上仅观察到近似的二重旋转对称性。因此,先前关于Z带的模型,即从一条肌动蛋白丝末端发出四条相同且旋转对称的连接并跨越到相邻肌节中四条肌动蛋白丝末端的模型是不正确的。