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

Author

Listed:
  • Andrew C. Hunt

    (Northwestern University
    Northwestern University)

  • Bastian Vögeli

    (Northwestern University
    Northwestern University)

  • Ahmed O. Hassan

    (Washington University School of Medicine)

  • Laura Guerrero

    (Northwestern University
    Northwestern University)

  • Weston Kightlinger

    (Northwestern University
    Northwestern University)

  • Danielle J. Yoesep

    (Northwestern University
    Northwestern University)

  • Antje Krüger

    (Northwestern University
    Northwestern University)

  • Madison DeWinter

    (Northwestern University
    Northwestern University
    Northwestern University Feinberg School of Medicine)

  • Michael S. Diamond

    (Washington University School of Medicine
    Washington University School of Medicine
    Washington University School of Medicine
    Washington University School of Medicine)

  • Ashty S. Karim

    (Northwestern University
    Northwestern University)

  • Michael C. Jewett

    (Northwestern University
    Northwestern University
    Northwestern University
    Northwestern University)

Abstract

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.

Suggested Citation

  • Andrew C. Hunt & Bastian Vögeli & Ahmed O. Hassan & Laura Guerrero & Weston Kightlinger & Danielle J. Yoesep & Antje Krüger & Madison DeWinter & Michael S. Diamond & Ashty S. Karim & Michael C. Jewett, 2023. "A rapid cell-free expression and screening platform for antibody discovery," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-38965-w
    DOI: 10.1038/s41467-023-38965-w
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