Reinhardt-Maelicke S, Kurz S, Sewing S, Stocker M, Pongs O
Institut für Physiologische Chemie, Johannes-Gutenberg-Universität, Mainz, Germany.
Eur J Biochem. 1993 Sep 15;216(3):871-7. doi: 10.1111/j.1432-1033.1993.tb18209.x.
Monoclonal antibodies were raised against a fusion protein consisting of a fragment of 141 amino acids of the C-terminal region of the rat brain voltage-gated K(+)-channel protein (RCK1) and the lambda N protein (fusion protein I). Selection of K(+)-channel-specific hybridoma cell lines was performed by means of an ELISA employing a fusion protein consisting of the K(+)-channel-specific peptide sequence and glutathione S-transferase (fusion protein II). For final selection of RCK1 isoform-specific antibodies, a panel of Xenopus oocytes was employed, each injected with cRNA coding for a specific RCK isoform (RCK 1, 2, 4 or 5). Several days after injection, cryosections of embedded oocytes were obtained and were employed in immunohistochemical analysis of antibody binding. Of five hybridoma supernatants from stable growing hybridoma cell lines, selected by the fusion-protein ELISA, one monoclonal antibody (denoted K1C3) recognized exclusively the RCK1-protein isoform, with the other four exhibiting different levels of cross-reactivity with other K(+)-channel isoforms, or with unknown protein(s) of non-injected oocytes. The expression of the RCK1 protein in the postnatal brain was studied using, as far as we are aware, the first example of the application of such isoform-specific antibodies.
制备了针对一种融合蛋白的单克隆抗体,该融合蛋白由大鼠脑电压门控钾离子通道蛋白(RCK1)C末端区域的141个氨基酸片段和λN蛋白组成(融合蛋白I)。通过酶联免疫吸附测定(ELISA),使用由钾离子通道特异性肽序列和谷胱甘肽S-转移酶组成的融合蛋白(融合蛋白II)来筛选钾离子通道特异性杂交瘤细胞系。为了最终筛选RCK1亚型特异性抗体,使用了一组非洲爪蟾卵母细胞,每个卵母细胞都注射了编码特定RCK亚型(RCK 1、2、4或5)的cRNA。注射几天后,获取包埋卵母细胞的冷冻切片,并将其用于抗体结合的免疫组织化学分析。在通过融合蛋白ELISA筛选出的稳定生长的杂交瘤细胞系的五种杂交瘤上清液中,一种单克隆抗体(命名为K1C3)仅识别RCK1蛋白亚型,其他四种与其他钾离子通道亚型或未注射卵母细胞的未知蛋白表现出不同程度的交叉反应。据我们所知,使用这种亚型特异性抗体,首次研究了产后脑中RCK1蛋白的表达情况。