Takatsuka Shogo, Yamada Hiroyuki, Haniuda Kei, Ichihashi Marina, Chiba Joe, Kitamura Daisuke
Division of Molecular Biology, Research Institute for Biomedical Sciences (RIBS), Tokyo University of Science, Noda, Japan.
Department of Biological Science and Technology, Tokyo University of Science, Tokyo, Japan.
Bio Protoc. 2019 Feb 20;9(4):e3174. doi: 10.21769/BioProtoc.3174.
Membrane proteins such as cytokine receptors and G protein-coupled receptors can be drug targets. Recently, we have generated specific monoclonal antibodies (mAbs) against the mouse IL-9 receptor (IL-9R) and found that IL-9R on memory B cells have critical roles in T-dependent immune response. So far, most antibodies against cell surface proteins have been generated by immunization of animals with recombinant proteins produced in ) or peptides derived from the protein. However, such antibodies often fail to recognize native proteins on cell surfaces because these antigens lack posttranslational modification and natural protein conformations. To circumvent such problems, we have developed a mouse immunization method, the DNA-immunization utilizing hyaluronidase and GroEL. Herein, we report an application of the original mouse immunization method in rats to generate anti-mouse IL-9R mAbs which could react with the native form of mouse IL-9R on cell surfaces. Thus, we suggest that the DNA-immunization method is feasible for generating monoclonal antibodies against cell surface proteins in rats.
细胞因子受体和G蛋白偶联受体等膜蛋白可以成为药物靶点。最近,我们制备了针对小鼠白细胞介素9受体(IL-9R)的特异性单克隆抗体(mAb),并发现记忆B细胞上的IL-9R在T细胞依赖性免疫反应中起关键作用。到目前为止,大多数针对细胞表面蛋白的抗体是通过用体外产生的重组蛋白或源自该蛋白的肽免疫动物而产生的。然而,这类抗体往往无法识别细胞表面的天然蛋白,因为这些抗原缺乏翻译后修饰和天然蛋白构象。为了规避这些问题,我们开发了一种小鼠免疫方法,即利用透明质酸酶和GroEL的DNA免疫法。在此,我们报告了将原始小鼠免疫方法应用于大鼠以产生可与细胞表面小鼠IL-9R天然形式反应的抗小鼠IL-9R单克隆抗体。因此,我们认为DNA免疫法对于在大鼠中产生针对细胞表面蛋白的单克隆抗体是可行的。