Katayama E, Wakabayashi T
J Biochem. 1981 Sep;90(3):703-14. doi: 10.1093/oxfordjournals.jbchem.a133524.
Heavy meromyosin (HMM) prepared by chymotryptic digestion retains DTNB light chain and subfragment-2 (S2) in addition to the two subfragment-1 (S1) moieties. The electron micrograph of negatively stained rigor complex of HMM and actin showed some different features as compared with that of S1 and actin. The three-dimensional image reconstructed from the electron micrograph of actin-HMM gave additional domains other than those observed in actin-S1 (Wakabayashi and Toyoshima, 1981). The differences between the images of actin-HMM and actin-S1 were attributed to the differences in protein composition. Further, the structural characteristics of actin-HMM are discussed in comparison with those of the actin-S1.
通过胰凝乳蛋白酶消化制备的重酶解肌球蛋白(HMM)除了两个亚片段-1(S1)部分外,还保留了二硫硝基苯甲酸轻链和亚片段-2(S2)。与S1和肌动蛋白的负染僵直复合物的电子显微照片相比,HMM和肌动蛋白的负染僵直复合物的电子显微照片显示出一些不同的特征。从肌动蛋白-HMM的电子显微照片重建的三维图像给出了在肌动蛋白-S1中未观察到的额外结构域(若林和丰岛,1981年)。肌动蛋白-HMM和肌动蛋白-S1图像之间的差异归因于蛋白质组成的差异。此外,还将肌动蛋白-HMM的结构特征与肌动蛋白-S1的结构特征进行了比较讨论。