Mimura N, Asano A
J Cell Biol. 1982 Jun;93(3):899-909. doi: 10.1083/jcb.93.3.899.
Actinogelin, which induces gelation of F-actin at Ca2+ concentrations below micromolar concentrations but not at higher concentrations, was isolated in the pure state from Ehrlich tumor cells. The protein consists of subunits of 112,000-115,000 daltons and under physiological conditions is present mostly as a dimer. Up to 1 mol of actinogelin (dimer) binds to 10-12 mol of actin monomer. The binding was slightly decreased by the presence of 50 microM Ca2+ and almost completely inhibited by 300 mM KCl. Antibodies against actinogelin giving a single precipitation line with Ehrlich cell extract and with pure actinogelin were raised in rabbits. Antibody preparations were purified before use in an affinity column containing purified actinogelin. In mouse embryo fibroblasts and 3T3 cells, staining of actin bundles by the antiactinogelin antibody usually was discontinuous or gave a striated appearance. Most of the crossing points of the actin bundles were intensively stained. In epithelial cells from mouse small intestine, actinogelin was distributed throughout the cell, with the exception of the microvilli, which were devoid of staining. In mouse peritoneal cells, the antibody staining patterns were similar to those of tetramethylrhodamine isothiocyanate-labeled heavy meromyosin, but the former usually were sharper than the latter. Intracellular localization of actinogelin was drastically altered by cytochalasin D treatment at 10 microgram/ml. We conclude that actinogelin is present in a wide variety of cell types and discuss the possible participation of actinogelin in the Ca2+-dependent regulation of microfilament distribution.
肌动凝胶蛋白在微摩尔浓度以下的钙离子浓度时可诱导F-肌动蛋白凝胶化,而在较高浓度时则不能,它是从艾氏瘤细胞中以纯态分离得到的。该蛋白质由112,000 - 115,000道尔顿的亚基组成,在生理条件下主要以二聚体形式存在。每摩尔肌动凝胶蛋白(二聚体)最多可结合10 - 12摩尔肌动蛋白单体。50微摩尔钙离子的存在会使结合略有下降,而300毫摩尔氯化钾则几乎完全抑制结合。用兔制备了针对肌动凝胶蛋白的抗体,该抗体与艾氏细胞提取物及纯肌动凝胶蛋白产生单一沉淀线。抗体制剂在用于含有纯化肌动凝胶蛋白的亲和柱之前进行了纯化。在小鼠胚胎成纤维细胞和3T3细胞中,抗肌动凝胶蛋白抗体对肌动蛋白束的染色通常是不连续的或呈现条纹状外观。肌动蛋白束的大多数交叉点被强烈染色。在小鼠小肠上皮细胞中,肌动凝胶蛋白分布于整个细胞,但微绒毛除外,微绒毛无染色。在小鼠腹腔细胞中,抗体染色模式与异硫氰酸四甲基罗丹明标记的重酶解肌球蛋白相似,但前者通常比后者更清晰。用10微克/毫升的细胞松弛素D处理后,肌动凝胶蛋白的细胞内定位发生了显著改变。我们得出结论,肌动凝胶蛋白存在于多种细胞类型中,并讨论了肌动凝胶蛋白可能参与微丝分布的钙离子依赖性调节。