Wachsberger P R, Pepe F A
J Cell Biol. 1980 Apr;85(1):33-41. doi: 10.1083/jcb.85.1.33.
The specific contributions of this work may be summarized as follows: (a) No hybridization of uterine and skeletal myosin occurs at pH 6.0 although previous studies have shown that hybridization does occur at pH 6.5 (B. Kaminer et al. 1976. J. Mol. Biol. 100:379-386) or 7.0 (T. Pollard. 1975. J. Cell Biol. 67:93-104) (b) Hybridization of uterine and skeletal light meromyosins (LMM) occurs at pH 7.0 but not at pH 6.0, which is analogous to the hybridization of myosins. (c) In hybridized paracrystals there is a uniform distribution of both uterine and skeletal LMM molecules because all the paracrystals have only one axial repeat pattern. This makes it highly likely that in hybridized filaments the two myosins are also uniformly distributed throughout the filaments. (d) The 14-nm repeat of white bands observed in paracrystals of uterine LMM formed at pH 6.0, compared with the 14-nm repeat of dark bands observed with skeletal LMM under the same conditions, probably reflects differences in surface charge density along the different LMM molecules.
(a) 在pH 6.0时子宫肌球蛋白和骨骼肌肌球蛋白不会发生杂交,尽管先前的研究表明在pH 6.5(B. 卡米纳等人,1976年。《分子生物学杂志》100:379 - 386)或pH 7.0(T. 波拉德,1975年。《细胞生物学杂志》67:93 - 104)时会发生杂交;(b) 子宫轻酶解肌球蛋白(LMM)和骨骼肌轻酶解肌球蛋白在pH 7.0时会发生杂交,但在pH 6.0时不会,这与肌球蛋白的杂交情况类似;(c) 在杂交副晶体中,子宫和骨骼肌LMM分子均匀分布,因为所有副晶体只有一种轴向重复模式。这使得杂交细丝中两种肌球蛋白也很可能在整个细丝中均匀分布;(d) 在pH 6.0形成的子宫LMM副晶体中观察到的白色条带的14纳米重复,与在相同条件下骨骼肌LMM观察到的深色条带的14纳米重复相比,可能反映了不同LMM分子表面电荷密度的差异。