Glenney J R, Tack B, Powell M A
J Cell Biol. 1987 Mar;104(3):503-11. doi: 10.1083/jcb.104.3.503.
Three forms of calpactin, the 36,000 Mr Ca++-binding cytoskeletal protein, were isolated in large amounts from bovine lung and human placenta using cycles of calcium-dependent precipitation followed by solubilization with EGTA-containing buffers. Calpactin-I as a tetramer of heavy (36 kD) and light (11 kD) chains was the predominant form of calpactin isolated, however milligram amounts of the calpactin-I heavy chain monomer and calpactin-II, a related but distinct molecule, were also isolated by this method. Calpactin-II was characterized in some detail and found to bind two Ca++ ions with Kd's of 10 microM in the presence of phosphatidylserine. Both calpactin-I and -II were found to aggregate liposomes at micromolar Ca++ concentrations, suggesting that at least two phospholipid-binding sites are present on these molecules. Both calpactin monomers bind to and bundle actin filament at high (1 mM) but not low (less than 1 microM) Ca++ concentrations. Amino-terminal sequence analysis of a lower molecular mass variant of calpactin-II revealed that this protein was the previously identified human "lipocortin" molecule. Antibodies were elicited to calpactin-I and -II and the cell and subcellular distribution of each was compared. Calpactin-II was only present at high levels in tissues (lung, placenta) which contained high levels of calpactin-I. Other tissues (intestine) contained high calpactin-I and undetectable levels of calpactin-II. Double-label immunofluorescence microscopy on human fibroblasts revealed that, like calpactin-I, calpactin-II is present in a submembraneous reticular network, although the distribution of the two calpactins is not identical.
通过钙依赖性沉淀循环,随后用含乙二醇双四乙酸(EGTA)的缓冲液溶解,从牛肺和人胎盘中大量分离出三种形式的凝溶胶蛋白(一种分子量为36,000的钙离子结合细胞骨架蛋白)。作为重链(36kD)和轻链(11kD)四聚体的凝溶胶蛋白-I是分离出的凝溶胶蛋白的主要形式,不过通过这种方法也分离出了毫克量的凝溶胶蛋白-I重链单体和凝溶胶蛋白-II(一种相关但不同的分子)。对凝溶胶蛋白-II进行了较为详细的表征,发现在磷脂酰丝氨酸存在的情况下,它能以10微摩尔的解离常数结合两个钙离子。发现在微摩尔钙离子浓度下,凝溶胶蛋白-I和-II都能使脂质体聚集,这表明这些分子上至少存在两个磷脂结合位点。两种凝溶胶蛋白单体在高钙离子浓度(1毫摩尔)而非低钙离子浓度(小于1微摩尔)下都能结合并捆绑肌动蛋白丝。对凝溶胶蛋白-II的一种低分子量变体进行的氨基末端序列分析表明,该蛋白就是先前鉴定出的人“脂皮质素”分子。制备了针对凝溶胶蛋白-I和-II的抗体,并比较了它们在细胞和亚细胞水平的分布。凝溶胶蛋白-II仅在含有高水平凝溶胶蛋白-I的组织(肺、胎盘)中高水平存在。其他组织(肠道)含有高浓度的凝溶胶蛋白-I,但未检测到凝溶胶蛋白-II。对人成纤维细胞进行的双标记免疫荧光显微镜检查显示,与凝溶胶蛋白-I一样,凝溶胶蛋白-II也存在于膜下网状网络中,尽管这两种凝溶胶蛋白的分布并不相同。