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Nanobody Repertoires for Exposing Vulnerabilities of SARS-CoV-2
Peter C Fridy; Natalia E Ketaren; Junjie Wang; Erica Y Jacobs; Tanmoy Sanyal; Kelly R Molloy; Fabian Schmidt; Magda Rutkowska; Yiska Weisblum; Sarah Keegan; Jacob B Jiler; Milana E Stein; Paul Dominic B Olinares; Theodora Hatziioannou; David Fenyö; Andej Sali; Paul D Bieniasz; Brian T Chait; Michael P Rout.
Affiliation
  • Peter C Fridy; The Rockefeller University
  • Natalia E Ketaren; The Rockefeller University
  • Junjie Wang; The Rockefeller University
  • Erica Y Jacobs; The Rockefeller University
  • Tanmoy Sanyal; University of California, San Francisco
  • Kelly R Molloy; The Rockefeller University
  • Fabian Schmidt; The Rockefeller University
  • Magda Rutkowska; The Rockefeller University
  • Yiska Weisblum; The Rockefeller University
  • Sarah Keegan; New York University
  • Jacob B Jiler; The Rockefeller University
  • Milana E Stein; The Rockefeller University
  • Paul Dominic B Olinares; The Rockefeller University
  • Theodora Hatziioannou; The Rockefeller University
  • David Fenyö; New York University
  • Andej Sali; University of California, San Francisco
  • Paul D Bieniasz; The Rockefeller University
  • Brian T Chait; The Rockefeller University
  • Michael P Rout; The Rockefeller University
Preprint in En | PREPRINT-BIORXIV | ID: ppbiorxiv-438911
ABSTRACT
Despite the great promise of vaccines, the COVID-19 pandemic is ongoing and future serious outbreaks are highly likely, so that multi-pronged containment strategies will be required for many years. Nanobodies are the smallest naturally occurring single domain antigen binding proteins identified to date, possessing numerous properties advantageous to their production and use. We present a large repertoire of high affinity nanobodies against SARS-CoV-2 Spike protein with excellent kinetic and viral neutralization properties, which can be strongly enhanced with oligomerization. This repertoire samples the epitope landscape of the Spike ectodomain inside and outside the receptor binding domain, recognizing a multitude of distinct epitopes and revealing multiple neutralization targets of pseudoviruses and authentic SARS-CoV-2, including in primary human airway epithelial cells. Combinatorial nanobody mixtures show highly synergistic activities, and are resistant to mutational escape and emerging viral variants of concern. These nanobodies establish an exceptional resource for superior COVID-19 prophylactics and therapeutics.
License
cc_by_nc_nd
Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Language: En Year: 2021 Document type: Preprint
Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Language: En Year: 2021 Document type: Preprint