A rapid cell-free expression and screening platform for antibody discovery

被引:11
|
作者
Hunt, Andrew C. [1 ,2 ]
Voegeli, Bastian [1 ,2 ]
Hassan, Ahmed O. [3 ]
Guerrero, Laura [1 ,2 ]
Kightlinger, Weston [1 ,2 ]
Yoesep, Danielle J. [1 ,2 ]
Krueger, Antje [1 ,2 ]
DeWinter, Madison [1 ,2 ,4 ]
Diamond, Michael S. [3 ,5 ,6 ,7 ]
Karim, Ashty S. [1 ,2 ]
Jewett, Michael C. [1 ,2 ,8 ,9 ,10 ]
机构
[1] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL 60208 USA
[2] Northwestern Univ, Ctr Synthet Biol, Evanston, IL 60208 USA
[3] Washington Univ, Dept Med, Sch Med, St Louis, MO 63110 USA
[4] Northwestern Univ, Med Scientist Training Program, Feinberg Sch Med, Chicago, IL 60611 USA
[5] Washington Univ, Dept Mol Microbiol, Sch Med, St Louis, MO 63110 USA
[6] Washington Univ, Dept Pathol & Immunol, Sch Med, St Louis, MO 63110 USA
[7] Washington Univ, Andrew M & Jane M Bursky Ctr Human Immunol & Immun, Sch Med, St Louis, MO 63110 USA
[8] Northwestern Univ, Chem Life Proc Inst, Evanston, IL 60208 USA
[9] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
[10] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
RECEPTOR-BINDING DOMAIN; ESCHERICHIA-COLI; PROTEIN; ASSAYS; FAB;
D O I
10.1038/s41467-023-38965-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Antibody discovery is bottlenecked by the individual expression and evaluation of antigen specific hits. Here, the authors build an antibody screening workflow leveraging cell-free protein synthesis that enables expression and evaluation of hundreds of antibody fragments in less than 24 h. Antibody discovery is bottlenecked by the individual expression and evaluation of antigen-specific hits. Here, we address this bottleneck by developing a workflow combining cell-free DNA template generation, cell-free protein synthesis, and binding measurements of antibody fragments in a process that takes hours rather than weeks. We apply this workflow to evaluate 135 previously published antibodies targeting the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), including all 8 antibodies previously granted emergency use authorization for coronavirus disease 2019 (COVID-19), and demonstrate identification of the most potent antibodies. We also evaluate 119 anti-SARS-CoV-2 antibodies from a mouse immunized with the SARS-CoV-2 spike protein and identify neutralizing antibody candidates, including the antibody SC2-3, which binds the SARS-CoV-2 spike protein of all tested variants of concern. We expect that our cell-free workflow will accelerate the discovery and characterization of antibodies for future pandemics and for research, diagnostic, and therapeutic applications more broadly.
引用
收藏
页数:14
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