A novel lentiviral scFv display library for rapid optimization and selection of high affinity antibodies

作者：Qudsia, Sehar; Merugu, Siva B.; Mangukiya, Hitesh B.; Hema, Negi; Wu, Zhenghua^*; Li, Dawei^*

来源：Biochemical and Biophysical Research Communications, 2018, 499(1): 71-77.

DOI：10.1016/j.bbrc.2018.03.131

• Agtuzumab
• Lentivirus scFv display library
• Hotspot mutagenesis
• Optimization library

Antibody display libraries have become a popular technique to screen monoclonal antibodies for therapeutic purposes. An important aspect of display technology is to generate an optimization library by changing antibody affinity to antigen through mutagenesis and screening the high affinity antibody. In this study, we report a novel lentivirus display based optimization library antibody in which Agtuzumab scFv is displayed on cell membrane of HEK-293T cells. To generate an optimization library, hotspot mutagenesis was performed to achieve diverse antibody library. Based on sequence analysis of randomly selected clones, library size was estimated approximately to be 1.6 x 10(6). Lentivirus display vector was used to display scFv antibody on cell surface and flow cytometery was performed to check the antibody affinity to antigen. Membrane bound scFv antibodies were then converted to secreted antibody through cre/loxP recombination. One of the mutant clones, M8 showed higher affinity to antigen in flow cytometery analysis. Further characterization of cellular and secreted scFv through western blot showed that antibody affinity was increased by three fold after mutagenesis. This study shows successful construction of a novel antibody library and suggests that hotspot mutagenesis could prove a useful and rapid optimization tool to generate similar libraries with various degree of antigen affinity.

• 出版日期2018-4-30
• 单位上海交通大学