Giometti C S, Anderson N L
J Biol Chem. 1981 Nov 25;256(22):11840-6.
In an analysis of 12 human fibroblast cell lines by two-dimensional electrophoresis, one cell line (1493) was found to contain a major protein variant (Cytosk: 12; for the convention used in spot numbering, see Anderson, N. L. (1981) Proc. Natl. Acad. Sci. U. S. A. 78, 2407-2411) not present in any of the other 11 cell lines. Biochemical characterization of the variant protein included determination of its subcellular location, partial amino acid composition, behavior on sodium dodecyl sulfate (SDS) versus SDS/urea gels, and partial proteolytic digestion patterns. All of these methods showed that Cytosk:12 is related to Cytosk:11. Both proteins are located in the cytoskeleton, contain little cysteine or proline and no detectable tryptophan, shift together to a higher apparent molecular weight when electrophoresed in the presence of SDS and 8 M urea versus SDS alone, and have identical products after partial proteolysis according to Cleveland et al. (Cleveland, D. W., Fischer, S. G., Kirschner, M. W., and Laemmli, U. K. (1977) J. Biol. Chem. 252, 1102-1106). Preparation of nonmuscle tropomyosin resulted in the partial purification of both Cytosk:11 and :12. The data suggest that Cytosk:11 is fibroblast nonmuscle tropomyosin and that Cytosk:12 in cell line 1493 is a charge variant of that protein.
通过二维电泳对12种人成纤维细胞系进行分析时,发现其中一个细胞系(1493)含有一种主要的蛋白质变体(Cytosk: 12;关于斑点编号所采用的惯例,见Anderson, N. L. (1981) Proc. Natl. Acad. Sci. U. S. A. 78, 2407 - 2411),而其他11个细胞系中均不存在这种变体。对该变体蛋白的生化特性分析包括确定其亚细胞定位、部分氨基酸组成、在十二烷基硫酸钠(SDS)与SDS/尿素凝胶上的行为以及部分蛋白酶解模式。所有这些方法均表明Cytosk:12与Cytosk:11相关。这两种蛋白都位于细胞骨架中,半胱氨酸或脯氨酸含量很少且未检测到色氨酸,当在SDS和8 M尿素存在下进行电泳时,与单独使用SDS相比,它们会一起向更高的表观分子量迁移,并且根据Cleveland等人(Cleveland, D. W., Fischer, S. G., Kirschner, M. W., and Laemmli, U. K. (1977) J. Biol. Chem. 252, 1102 - 1106)的方法,部分蛋白酶解后具有相同的产物。非肌肉原肌球蛋白的制备导致Cytosk:11和Cytosk:12都得到了部分纯化。数据表明Cytosk:11是成纤维细胞非肌肉原肌球蛋白,而细胞系1493中的Cytosk:12是该蛋白的电荷变体。