Kurosawa Kohei, Lin Waka, Ohta Kunihiro
Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, Tokyo, Japan.
Methods Mol Biol. 2014;1060:139-48. doi: 10.1007/978-1-62703-586-6_8.
Here we describe a detailed protocol for the one-step preparation of antigen-specific human chimeric immunoglobulin G (IgG) monoclonal antibodies (mAbs) using an in vitro antibody design method referred to as the ADLib (Autonomously Diversifying Library) system. This method employs a chicken B cell line DT40-based library in which the variable regions of the Ig gene loci have been highly diversified by treatment with the histone deacetylase inhibitors. DT40 cells express both membrane-bound and secreted forms of chicken IgM. This property allows a rapid screening and selection of antibody-producing B cells from the library by using magnetic beads conjugated with any antigen of interest. To apply the ADLib system to the direct generation of human chimeric antibody, we have inserted a DNA segment coding for the constant region of human IgG into the chicken IgM heavy-chain locus of DT40 cells by homologous gene targeting. By a mechanism of alternative splicing, the resulting DT40 strain simultaneously expresses chimeric human IgG that contain the same Ig variable region sequences as the membrane-bound chicken IgM displayed at the cell surface. Application of the ADLib system to this human Ig-inserted DT40 strain enables the one-step isolation of human chimeric IgG that is specific for any antigen of interest and can be easily purified for immediate use.
在此,我们描述了一种详细的方案,用于使用一种称为ADLib(自主多样化文库)系统的体外抗体设计方法,一步制备抗原特异性人嵌合免疫球蛋白G(IgG)单克隆抗体(mAb)。该方法采用基于鸡B细胞系DT40的文库,其中Ig基因座的可变区通过组蛋白脱乙酰酶抑制剂处理而高度多样化。DT40细胞表达膜结合形式和分泌形式的鸡IgM。这一特性使得通过使用与任何感兴趣的抗原偶联的磁珠,能够从文库中快速筛选和选择产生抗体的B细胞。为了将ADLib系统应用于直接产生人嵌合抗体,我们通过同源基因靶向将编码人IgG恒定区的DNA片段插入DT40细胞的鸡IgM重链基因座。通过可变剪接机制,所得的DT40菌株同时表达嵌合人IgG,其包含与细胞表面展示的膜结合鸡IgM相同的Ig可变区序列。将ADLib系统应用于这种插入人Ig的DT40菌株,能够一步分离出对任何感兴趣的抗原具有特异性的人嵌合IgG,并且可以很容易地纯化以供立即使用。