Ogata K, Kurki P, Celis J E, Nakamura R M, Tan E M
Exp Cell Res. 1987 Feb;168(2):475-86. doi: 10.1016/0014-4827(87)90020-6.
Two hybridomas producing monoclonal antibodies to proliferating cell nuclear antigen. (PNCA)/cyclin were generated from spleen cells of BALB/c mice immunized with purified PCNA from rabbit thymus. The specificity of the monoclonal antibodies (19A2 and 19F4) was established by showing that they reacted in enzyme-linked immunosorbent assay (ELISA) with purified PCNA. Furthermore, they reacted in one-dimensional (ID) gel immunoblots with a 36 kD polypeptide which also reacted with human autoantibodies from lupus patients. Both monoclonals also recognized the nuclear polypeptide cyclin in two-dimensional (2D) gel immunoblots of HeLa cell proteins. Epitopes recognized by 19A2 and 19F4 were analysed by competitive inhibition test using a modified ELISA. The data suggested that the epitopes were closely related, but not identical. The data with human auto-antibodies were more difficult to interpret, although it suggested that some human anti-PCNA may share epitopes with 19A2 and 19F4, but in addition recognize different epitopes on the PCNA molecule.
从用兔胸腺纯化增殖细胞核抗原(PCNA)/细胞周期蛋白免疫的BALB/c小鼠脾细胞中产生了两种产生抗增殖细胞核抗原单克隆抗体的杂交瘤。通过显示单克隆抗体(19A2和19F4)在酶联免疫吸附测定(ELISA)中与纯化的PCNA发生反应,确定了其特异性。此外,它们在一维(ID)凝胶免疫印迹中与一种36kD的多肽发生反应,该多肽也与狼疮患者的人自身抗体发生反应。两种单克隆抗体在HeLa细胞蛋白质的二维(2D)凝胶免疫印迹中也识别核多肽细胞周期蛋白。使用改良的ELISA通过竞争抑制试验分析了19A2和19F4识别的表位。数据表明这些表位密切相关,但不相同。关于人自身抗体的数据更难解释,尽管这表明一些人抗PCNA可能与19A2和19F4共享表位,但此外还识别PCNA分子上的不同表位。