Liu Ju, Li Ruihua, Liu Kun, Li Liangliang, Zai Xiaodong, Chi Xiangyang, Fu Ling, Xu Junjie, Chen Wei
Laboratory of Vaccine and Antibody Engineering, Beijing Institute of Biotechnology, Beijing 100071, China.
Laboratory of Vaccine and Antibody Engineering, Beijing Institute of Biotechnology, Beijing 100071, China.
Biochem Biophys Res Commun. 2016 Apr 22;473(1):23-28. doi: 10.1016/j.bbrc.2016.03.038. Epub 2016 Mar 12.
High-throughput sequencing of the antibody repertoire provides a large number of antibody variable region sequences that can be used to generate human monoclonal antibodies. However, current screening methods for identifying antigen-specific antibodies are inefficient. In the present study, we developed an antibody clone screening strategy based on clone dynamics and relative frequency, and used it to identify antigen-specific human monoclonal antibodies. Enzyme-linked immunosorbent assay showed that at least 52% of putative positive immunoglobulin heavy chains composed antigen-specific antibodies. Combining information on dynamics and relative frequency improved identification of positive clones and elimination of negative clones. and increase the credibility of putative positive clones. Therefore the screening strategy could simplify the subsequent experimental screening and may facilitate the generation of antigen-specific antibodies.
抗体库的高通量测序可提供大量抗体可变区序列,这些序列可用于生成人单克隆抗体。然而,目前用于鉴定抗原特异性抗体的筛选方法效率低下。在本研究中,我们开发了一种基于克隆动态和相对频率的抗体克隆筛选策略,并将其用于鉴定抗原特异性人单克隆抗体。酶联免疫吸附测定表明,至少52%的推定阳性免疫球蛋白重链构成了抗原特异性抗体。结合动态和相对频率信息可改善阳性克隆的鉴定并消除阴性克隆,并提高推定阳性克隆的可信度。因此,该筛选策略可简化后续的实验筛选,并可能有助于生成抗原特异性抗体。