抗极低密度脂蛋白受体单克隆抗体的大量制备及纯化

背景：极低密度脂蛋白受体被认为是一种“瑞士军刀”样多功能受体，对该受体的研究很广泛，但其商品化抗体种类较少，价格偏贵。 目的：获得研究可用的抗极低密度脂蛋白受体的单克隆抗体。 方法：为了获得抗极低密度脂蛋白受体单克隆抗体，选用可分泌针对极低密度脂蛋白受体胞内段的单克隆抗体的杂交瘤细胞IgG 6A6。通过将杂交瘤细胞IgG 6A6注入Balb/c小鼠腹腔内，2周后收集腹水，分别通过盐析法(正辛酸-饱和硫酸铵沉淀法)初步纯化和亲和层析进一步纯化目的蛋白，获得针对极低密度脂蛋白受体胞内段的单克隆抗体。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳检测其相对分子质量和纯度，酶联免疫吸附实验检测其活性。 结果与结论：未纯化腹水Western Blotting结果显示条带较多，背景不干净；而经正辛酸-饱和硫酸铵法初步纯化的腹水、经Protein A进一步纯化得到的抗体均可特异识别极低密度脂蛋白受体。提示经盐析法和Protein A Agarose纯化可获得较纯和有活性的单克隆抗

Preparation and purification of a great amount of monoclonal antibodies against the c-terminal of very low density lipoprotein receptor

BACKGROUND:Very low density lipoprotein receptor is regarded as a Swiss Army Knife receptor, and many researchers have studied this receptor. But there are only several kinds of commercial antibodies and the price is on the high side. OBJECTIVE:To get the monoclonal antibody against the c-terminal of very low density lipoprotein receptor for the future study. METHODS:In order to obtain the very low density lipoprotein receptor, hybridoma IgG 6A6 cells related with very low density lipoprotein receptor intracellular domain was injected into peritoneal of Balb/c mice. After 2 weeks, ascites was collected, and the target protein was preliminary purified by salting-out method (n-octanoic acid-saturated ammonium sulfate precipitation method) and further purified by affinity chromatography, and the monoclonal antibody related with very low density lipoprotein receptor intracellular domain was obtained. The relative molecular mass and purity were detected by sodium dodecyl sulfate polyacrylamide gel electrophoresis, and the activity was detected by enzyme-linked immunosorbent assay. RESULTS AND CONCLUSION:Western Blotting results showed that the antibody from the ascites directly can bind the very low density lipoprotein receptor protein, but the background was not clear. The purified antibody from the ascites through salting-out method (n-octanoic acid-saturated ammonium sulfate precipitation method) and then by protein A affinity chromatography can bind specifically with the very low density lipoprotein receptor. The pure and activity monoclonal antibodies can be obtained through purification by the salting-out method and Protein A Agarose