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Nanobody Repertoires for Exposing Vulnerabilities of SARS-CoV-2

View ORCID ProfileFred D. Mast, View ORCID ProfilePeter C. Fridy, Natalia E. Ketaren, Junjie Wang, Erica Y. Jacobs, View ORCID ProfileJean Paul Olivier, View ORCID ProfileTanmoy Sanyal, Kelly R. Molloy, View ORCID ProfileFabian Schmidt, Magda Rutkowska, View ORCID ProfileYiska Weisblum, Lucille M. Rich, Elizabeth R. Vanderwall, Nicolas Dambrauskas, Vladimir Vigdorovich, Sarah Keegan, Jacob B. Jiler, Milana E. Stein, Paul Dominic B. Olinares, Theodora Hatziioannou, View ORCID ProfileD. Noah Sather, Jason S. Debley, View ORCID ProfileDavid Fenyö, Andrej Sali, Paul D. Bieniasz, View ORCID ProfileJohn D. Aitchison, View ORCID ProfileBrian T. Chait, View ORCID ProfileMichael P. Rout
doi: https://doi.org/10.1101/2021.04.08.438911
Fred D. Mast
1Center for Global Infectious Disease Research, Seattle Children’s Research Institute, Seattle, Washington, USA
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  • ORCID record for Fred D. Mast
Peter C. Fridy
2Laboratory of Cellular and Structural Biology, The Rockefeller University, New York, New York 10065, USA
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Natalia E. Ketaren
2Laboratory of Cellular and Structural Biology, The Rockefeller University, New York, New York 10065, USA
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Junjie Wang
3Laboratory of Mass Spectrometry and Gaseous Ion Chemistry, The Rockefeller University, New York, New York 10065, USA
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Erica Y. Jacobs
3Laboratory of Mass Spectrometry and Gaseous Ion Chemistry, The Rockefeller University, New York, New York 10065, USA
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Jean Paul Olivier
1Center for Global Infectious Disease Research, Seattle Children’s Research Institute, Seattle, Washington, USA
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  • ORCID record for Jean Paul Olivier
Tanmoy Sanyal
4Department of Bioengineering and Therapeutic Sciences, Department of Pharmaceutical Chemistry, California Institute for Quantitative Biosciences, Byers Hall, 1700 4th Street, Suite 503B, University of California, San Francisco, San Francisco, CA 94158, USA
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Kelly R. Molloy
3Laboratory of Mass Spectrometry and Gaseous Ion Chemistry, The Rockefeller University, New York, New York 10065, USA
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Fabian Schmidt
5Laboratory of Retrovirology, The Rockefeller University, New York, New York 10065, USA
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  • ORCID record for Fabian Schmidt
Magda Rutkowska
5Laboratory of Retrovirology, The Rockefeller University, New York, New York 10065, USA
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Yiska Weisblum
5Laboratory of Retrovirology, The Rockefeller University, New York, New York 10065, USA
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  • ORCID record for Yiska Weisblum
Lucille M. Rich
6Center for Immunity and Immunotherapies, Seattle Children’s Research Institute, Seattle, Washington, USA
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Elizabeth R. Vanderwall
6Center for Immunity and Immunotherapies, Seattle Children’s Research Institute, Seattle, Washington, USA
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Nicolas Dambrauskas
1Center for Global Infectious Disease Research, Seattle Children’s Research Institute, Seattle, Washington, USA
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Vladimir Vigdorovich
1Center for Global Infectious Disease Research, Seattle Children’s Research Institute, Seattle, Washington, USA
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Sarah Keegan
7Center for Health Informatics and Bioinformatics, New York University School of Medicine, New York, NY, USA
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Jacob B. Jiler
2Laboratory of Cellular and Structural Biology, The Rockefeller University, New York, New York 10065, USA
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Milana E. Stein
2Laboratory of Cellular and Structural Biology, The Rockefeller University, New York, New York 10065, USA
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Paul Dominic B. Olinares
3Laboratory of Mass Spectrometry and Gaseous Ion Chemistry, The Rockefeller University, New York, New York 10065, USA
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Theodora Hatziioannou
5Laboratory of Retrovirology, The Rockefeller University, New York, New York 10065, USA
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D. Noah Sather
1Center for Global Infectious Disease Research, Seattle Children’s Research Institute, Seattle, Washington, USA
8Department of Pediatrics, University of Washington, Seattle, Washington, USA
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Jason S. Debley
6Center for Immunity and Immunotherapies, Seattle Children’s Research Institute, Seattle, Washington, USA
8Department of Pediatrics, University of Washington, Seattle, Washington, USA
9Division of Pulmonary and Sleep Medicine, Seattle Children’s Hospital, Seattle, Washington, USA
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David Fenyö
7Center for Health Informatics and Bioinformatics, New York University School of Medicine, New York, NY, USA
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Andrej Sali
4Department of Bioengineering and Therapeutic Sciences, Department of Pharmaceutical Chemistry, California Institute for Quantitative Biosciences, Byers Hall, 1700 4th Street, Suite 503B, University of California, San Francisco, San Francisco, CA 94158, USA
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Paul D. Bieniasz
5Laboratory of Retrovirology, The Rockefeller University, New York, New York 10065, USA
10Howard Hughes Medical Institute, The Rockefeller University, New York, New York 10065, USA
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John D. Aitchison
1Center for Global Infectious Disease Research, Seattle Children’s Research Institute, Seattle, Washington, USA
8Department of Pediatrics, University of Washington, Seattle, Washington, USA
11Department of Biochemistry, University of Washington, Seattle, Washington, USA
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  • For correspondence: [email protected]
Brian T. Chait
3Laboratory of Mass Spectrometry and Gaseous Ion Chemistry, The Rockefeller University, New York, New York 10065, USA
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Michael P. Rout
2Laboratory of Cellular and Structural Biology, The Rockefeller University, New York, New York 10065, USA
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  • For correspondence: [email protected]
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SUMMARY

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.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted April 10, 2021.
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Nanobody Repertoires for Exposing Vulnerabilities of SARS-CoV-2
Fred D. Mast, Peter C. Fridy, Natalia E. Ketaren, Junjie Wang, Erica Y. Jacobs, Jean Paul Olivier, Tanmoy Sanyal, Kelly R. Molloy, Fabian Schmidt, Magda Rutkowska, Yiska Weisblum, Lucille M. Rich, Elizabeth R. Vanderwall, Nicolas Dambrauskas, Vladimir Vigdorovich, Sarah Keegan, Jacob B. Jiler, Milana E. Stein, Paul Dominic B. Olinares, Theodora Hatziioannou, D. Noah Sather, Jason S. Debley, David Fenyö, Andrej Sali, Paul D. Bieniasz, John D. Aitchison, Brian T. Chait, Michael P. Rout
bioRxiv 2021.04.08.438911; doi: https://doi.org/10.1101/2021.04.08.438911
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Nanobody Repertoires for Exposing Vulnerabilities of SARS-CoV-2
Fred D. Mast, Peter C. Fridy, Natalia E. Ketaren, Junjie Wang, Erica Y. Jacobs, Jean Paul Olivier, Tanmoy Sanyal, Kelly R. Molloy, Fabian Schmidt, Magda Rutkowska, Yiska Weisblum, Lucille M. Rich, Elizabeth R. Vanderwall, Nicolas Dambrauskas, Vladimir Vigdorovich, Sarah Keegan, Jacob B. Jiler, Milana E. Stein, Paul Dominic B. Olinares, Theodora Hatziioannou, D. Noah Sather, Jason S. Debley, David Fenyö, Andrej Sali, Paul D. Bieniasz, John D. Aitchison, Brian T. Chait, Michael P. Rout
bioRxiv 2021.04.08.438911; doi: https://doi.org/10.1101/2021.04.08.438911

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