Seymour J, O'Brien E J
J Muscle Res Cell Motil. 1985 Dec;6(6):725-55. doi: 10.1007/BF00712239.
Negatively stained paracrystals of reconstituted thin filaments decorated with myosin subfragment 1 (S1), at high calcium concentrations (greater than or equal to 10(-5) M), exhibit pgg plane group symmetry with component filaments having 28 subunits in 13 turns of the actin genetic helix. Isolated S1 decorated F-actin filaments trapped in a stain film were also observed to form spontaneously paracrystals with pgg plane group symmetry. We conclude that a favourable S1-S1 interaction must exist in order to stabilize these structures. Three-dimensional helical reconstructions, calculated from these paracrystals show S1 to be curved, 12 to 14 nm long and tilted with respect to the helical axis, in broad agreement with previous reconstructions calculated from isolated particles. Reconstructions of S1 and HMM decorated filaments that resolve actin show a principal myosin binding site located on the side of the actin subunit reported by Taylor & Amos [J. molec. Biol. 147, 297-324 (1981)] and a possible small interaction on the opposite side. The appearance, symmetry and helical reconstructions of isolated F-actin filaments decorated with heavy meromyosin (HMM) were similar to those of S1 decorated filaments, except at high radii where extra mass was observed. This probably arose from the connection between the two heads of HMM bound to the same long-pitch strand of actin. In contrast to most studies on thin filaments, which use reconstituted filaments, we present data on natural I-segments of muscle homogenates. Individual filaments exhibited actin helical symmetry which on reconstruction gave a two-domain motif oriented consistently with its long axis approximately perpendicular to the helical axis, but inclined towards the 5.9 nm genetic helix. Our original interpretation of these maps [Seymour & O'Brien, Nature, Lond. 283, 680-2 (1980)] depended upon reconstructions from F-actin paracrystals, which suggested actin was rather symmetrical in shape. New data from two- and three-dimensional crystal studies and reconstructions of actin-tropomyosin filaments show that actin is rather elongated and consists of two domains. These results indicate that actin contributes towards both domains of our I-segment motif and are consistent with the monomer long axis lying approximately perpendicular to the helical axis. Although tropomyosin is not resolved, comparison of the actin-tropomyosin and I-segment reconstructions suggests that tropomyosin is strongly merged with the actin domain at a lower radius from the helical axis and that the domain at higher radius arises solely from actin.
在高钙浓度(大于或等于10⁻⁵ M)下,用肌球蛋白亚片段1(S1)修饰的重构细肌丝的负染副晶体,呈现pgg平面群对称性,其组成细丝在肌动蛋白遗传螺旋的13圈中有28个亚基。还观察到被困在染色膜中的分离的S1修饰的F-肌动蛋白丝自发形成具有pgg平面群对称性的副晶体。我们得出结论,为了稳定这些结构,必须存在有利的S1-S1相互作用。从这些副晶体计算出的三维螺旋重建显示,S1是弯曲的,长12至14 nm,相对于螺旋轴倾斜,这与先前从分离颗粒计算出的重建结果大致一致。对解析出肌动蛋白的S1和重酶解肌球蛋白(HMM)修饰的细丝的重建显示,主要的肌球蛋白结合位点位于泰勒和阿莫斯报道的肌动蛋白亚基的一侧[《分子生物学杂志》147, 297 - 324 (1981)],而在另一侧可能存在小的相互作用。用HMM修饰的分离的F-肌动蛋白丝的外观、对称性和螺旋重建与用S1修饰的细丝相似,只是在高半径处观察到额外的质量。这可能源于与同一条长间距肌动蛋白链结合的HMM的两个头部之间的连接。与大多数关于细肌丝的研究不同,那些研究使用的是重构细丝,我们展示了关于肌肉匀浆天然I段的数据。单个细丝呈现出肌动蛋白螺旋对称性,重建后得到一个两结构域基序,其长轴大致垂直于螺旋轴,且向5.9 nm的遗传螺旋倾斜。我们对这些图谱的最初解释[西摩和奥布赖恩,《自然》,伦敦283, 680 - 2 (1980)]依赖于F-肌动蛋白副晶体的重建,这表明肌动蛋白形状相当对称。来自二维和三维晶体研究以及肌动蛋白-原肌球蛋白细丝重建的新数据表明,肌动蛋白相当细长,由两个结构域组成。这些结果表明,肌动蛋白对我们I段基序的两个结构域都有贡献,并且与单体长轴大致垂直于螺旋轴一致。尽管原肌球蛋白未被解析,但肌动蛋白-原肌球蛋白和I段重建的比较表明,原肌球蛋白在离螺旋轴较低半径处与肌动蛋白结构域强烈融合,而在较高半径处的结构域仅由肌动蛋白产生。