Biomaterials Research Group, Health and Medical Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Higashi, Tsukuba 305-8566, Japan.
Department of Biochemistry, Bio-Peak Co., Ltd., 584-70 Shimonojo, Takasaki 370-0854, Japan.
Molecules. 2020 Jun 24;25(12):2905. doi: 10.3390/molecules25122905.
Screening antibody libraries is an important step in establishing recombinant monoclonal antibodies. The colony assay can identify positive clones without almost any false-positives; however, its antibody library is smaller than those used in other recombinant screening methods such as phage display. Thus, to improve the efficiency of colony assays, it is necessary to increase library size per screening. Here, we report developing a colony assay with single-chain variable fragment (scFv) fused to the N-terminus of bacterial alkaline phosphatase (scFv-PhoA). The scFv-PhoA library was constructed in an expression vector specifically designed for this study. Use of this library allowed the successful and direct detection of positive clones exhibiting PhoA activity, without the need for a secondary antibody. Colony assay screening with scFv-PhoA is simple, rapid, offers a higher success rate than previous methods based on scFv libraries, and-most importantly-it enables high-throughput procedures.
筛选抗体库是建立重组单克隆抗体的重要步骤。集落测定法可以在几乎没有任何假阳性的情况下鉴定出阳性克隆;然而,其抗体库比其他重组筛选方法(如噬菌体展示)中使用的抗体库要小。因此,为了提高集落测定法的效率,有必要增加每次筛选的文库大小。在这里,我们报告了一种用与碱性磷酸酶(scFv-PhoA)的 N 端融合的单链可变片段(scFv)开发的集落测定法。scFv-PhoA 文库构建在专门为此研究设计的表达载体中。使用该文库可以成功且直接检测到表现出 PhoA 活性的阳性克隆,而无需使用二抗。用 scFv-PhoA 进行集落测定法筛选简单、快速,成功率高于以前基于 scFv 文库的方法,最重要的是,它可以实现高通量的操作。