Katayama E, Nonomura Y
J Biochem. 1979 Nov;86(5):1511-22. doi: 10.1093/oxfordjournals.jbchem.a132669.
Negatively stained images of divalent cation-induced tropomyosin paracrystals show polymorphic patterns which are almost bipolar. Although these bipolar forms are naturally due to antiparallel arrays of molecules, the precise molecular arrangements have not been clarified yet except in the case of one type of these polymorphic paracrystals by Stewart and McLachlan [(1976) J. Mol. Biol. 103, 251--269]. In the previous paper we showed that the lead-induced polar paracrystal is a parallel and in-register array of tropomyosin molecules. Moreover, we have made it possible to locate a given residue on the staining pattern. By overlapping two photographic transparencies of the polar paracrystal antiparallel, directly observed images of polymorphic bipolar paracrystals could be synthesized photographically with fidelity. The overlap length between N-terminals of antiparallel pairs of molecules could be easily determined without any assumptions. Next, we considered the stabilizing forces involved in the morphogenesis of such polymorphic paracrystals. The cation-bridged attractive forces already proposed by some groups were insufficient to account for the stability of some specific forms of tropomyosin paracrystals. From the primary amino acid sequence of tropomyosin, we calculated the changes of repulsive forces between the basic residues with changes of molecular overlap length between the N-terminals of antiparallel pairs. By setting the values of charge appropriately, we could account well for the stability of the polymorphic structures observed by electron microscopy.
二价阳离子诱导的原肌球蛋白副晶体的负染图像显示出几乎呈双极的多晶型模式。尽管这些双极形式自然是由于分子的反平行排列所致,但除了斯图尔特和麦克拉克伦研究的一种多晶型副晶体情况外[(1976)《分子生物学杂志》103, 251 - 269],精确的分子排列尚未阐明。在之前的论文中我们表明,铅诱导的极性副晶体是原肌球蛋白分子的平行且对齐的排列。此外,我们已经能够在染色模式上定位特定的残基。通过将极性副晶体的两张照相透明片反平行重叠,可以逼真地合成多晶型双极副晶体的直接观察图像。分子反平行对的N端之间的重叠长度可以在没有任何假设的情况下轻松确定。接下来,我们考虑了这种多晶型副晶体形态发生过程中涉及的稳定力。一些研究小组已经提出的阳离子桥连吸引力不足以解释某些特定形式的原肌球蛋白副晶体的稳定性。根据原肌球蛋白的一级氨基酸序列,我们计算了反平行对的N端之间分子重叠长度变化时碱性残基之间排斥力的变化。通过适当地设定电荷值,我们能够很好地解释电子显微镜观察到的多晶型结构的稳定性。