Chantler P D
J Cell Biol. 1985 Jul;101(1):207-16. doi: 10.1083/jcb.101.1.207.
A protein complex is shown to participate in a calcium-dependent association with plasma membranes purified either from pig mesenteric lymph node lymphocytes or from human lymphoblastoid cell lines. Plasma membranes prepared in the presence of calcium possess this complex; those prepared in the absence of calcium (5 mM EGTA) do not. The complex associates itself with the inner cytoplasmic surface of the plasma membrane. This complex is referred to as the "acidic protein band" because of its location during migration upon alkaline-urea gel electrophoresis. The complex dissociates from the plasma membrane during electrophoresis on 8-M urea gels, irrespective of calcium levels during electrophoresis; at intermediate urea concentrations (4-6 M), the complex is not dissociated in the presence of calcium. Upon purification of the acidic protein band, SDS acrylamide gel electrophoresis, immunoblotting, and radioimmunoassay techniques suggest that the acidic protein band is composed of at least four peptides (designated 68K, 59K, 20K, 20K): two of these (68K, 20K) are immunopositive for calcineurin and one (20K) is immunopositive for calmodulin. Immunoblots of urea gels also indicate that the calcineurin heavy chain (68K) can also appear at three different locations on the urea gel. Patches and caps induced in human peripheral blood lymphocytes by fluorescein-conjugated goat anti-human IgG are not coincident with the location of calcineurin, which remains distributed throughout the cell.
已表明一种蛋白质复合物参与了与从猪肠系膜淋巴结淋巴细胞或人淋巴母细胞系纯化的质膜的钙依赖性结合。在有钙存在的情况下制备的质膜含有这种复合物;而在无钙(5 mM乙二醇双四乙酸)的情况下制备的质膜则没有。该复合物与质膜的内细胞质表面结合。由于其在碱性尿素凝胶电泳迁移过程中的位置,这种复合物被称为“酸性蛋白带”。在8 M尿素凝胶上进行电泳时,该复合物会从质膜上解离,无论电泳过程中的钙水平如何;在中等尿素浓度(4 - 6 M)下,该复合物在有钙存在时不会解离。纯化酸性蛋白带后,十二烷基硫酸钠聚丙烯酰胺凝胶电泳、免疫印迹和放射免疫测定技术表明,酸性蛋白带至少由四种肽组成(分别命名为68K、59K、20K、20K):其中两种(68K、20K)对钙调神经磷酸酶呈免疫阳性,一种(20K)对钙调蛋白呈免疫阳性。尿素凝胶的免疫印迹还表明,钙调神经磷酸酶重链(68K)也可出现在尿素凝胶上的三个不同位置。荧光素偶联的山羊抗人IgG在人外周血淋巴细胞中诱导产生的斑块和帽与钙调神经磷酸酶的位置不一致,钙调神经磷酸酶仍分布在整个细胞中。