Sung Lanping Amy, Vera Carlos
Department of Bioengineering, Jacobs School of Engineering, University of California, San Diego, La Jolla, CA 92093-0412, USA.
Ann Biomed Eng. 2003 Dec;31(11):1314-26. doi: 10.1114/1.1635820.
It is a long-standing mystery why erythrocyte actin filaments in the junctional complex (JC) are uniformly approximately 37 nm and the membrane skeleton consists of hexagons. We have previously proposed that a "molecular ruler" formed by E-tropomodulin and tropomyosin 5 or 5b functions to generate protofilaments of 12 G actin under mechanical stress. Here, we illustrate that intrinsic properties of actin filaments, e.g., turns, chemical bonds, and dimensions of the helix, also favor fragmentation into protofilaments under mechanical stress. We further construct a mechanical model in that a pair of G actin is wrapped around by a split alpha and beta spectrin, which may spin to two potential positions, and stabilize to one when the tail end is restricted. A reinforced protofilament may function as a mechanical axis to anchor three (top, middle, and bottom) pairs of Sp. Each Sp pair may wrap around the protofilament with a wide dihedral angle (approximately 166.2 degrees) and a minimal axial distance (2.75 nm). Such three Sp pairs may spiral down (right handed) the protofilament from the pointed end with a dihedral angle of approximately 55.4 degrees in between the Sp pairs. This first three-dimensional model of JC may explain the hexagonal geometry of the erythrocyte membrane skeleton.
长期以来,一个不解之谜是,连接复合体(JC)中的红细胞肌动蛋白丝为何均匀地约为37纳米,以及膜骨架为何由六边形组成。我们之前提出,由E - 原肌球蛋白和原肌球蛋白5或5b形成的“分子尺”在机械应力作用下发挥功能,生成由12个球形肌动蛋白组成的原纤维。在此,我们表明,肌动蛋白丝的内在特性,如螺旋的转角、化学键和尺寸,在机械应力作用下也有利于断裂成原纤维。我们进一步构建了一个力学模型,其中一对球形肌动蛋白被分裂的α和β血影蛋白包裹,该血影蛋白可能旋转到两个潜在位置,并在尾端受到限制时稳定在一个位置。一根强化的原纤维可能作为一个机械轴,锚定三对(顶部、中间和底部)血影蛋白。每对血影蛋白可能以较大的二面角(约166.2度)和最小的轴向距离(2.75纳米)缠绕原纤维。这样的三对血影蛋白可能从尖端部以约55.4度的二面角右旋螺旋向下缠绕原纤维。这个JC的首个三维模型可能解释红细胞膜骨架的六边形几何结构。