Multivalency transforms SARS-CoV-2 antibodies into ultrapotent neutralizers

Here, the authors combine three different antibody specificities and an Fc domain on a single multivalent molecule, resulting in high neutralization activity despite viral sequence variability.

Bibliographic Details
Main Authors: Edurne Rujas, Iga Kucharska, Yong Zi Tan, Samir Benlekbir, Hong Cui, Tiantian Zhao, Gregory A. Wasney, Patrick Budylowski, Furkan Guvenc, Jocelyn C. Newton, Taylor Sicard, Anthony Semesi, Krithika Muthuraman, Amy Nouanesengsy, Clare Burn Aschner, Katherine Prieto, Stephanie A. Bueler, Sawsan Youssef, Sindy Liao-Chan, Jacob Glanville, Natasha Christie-Holmes, Samira Mubareka, Scott D. Gray-Owen, John L. Rubinstein, Bebhinn Treanor, Jean-Philippe Julien
Format: Article
Language:English
Published: Nature Publishing Group 2021-06-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-021-23825-2
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spelling doaj-21239c53aca444dbbc85f54151271ca52021-06-20T11:13:41ZengNature Publishing GroupNature Communications2041-17232021-06-0112111210.1038/s41467-021-23825-2Multivalency transforms SARS-CoV-2 antibodies into ultrapotent neutralizersEdurne Rujas0Iga Kucharska1Yong Zi Tan2Samir Benlekbir3Hong Cui4Tiantian Zhao5Gregory A. Wasney6Patrick Budylowski7Furkan Guvenc8Jocelyn C. Newton9Taylor Sicard10Anthony Semesi11Krithika Muthuraman12Amy Nouanesengsy13Clare Burn Aschner14Katherine Prieto15Stephanie A. Bueler16Sawsan Youssef17Sindy Liao-Chan18Jacob Glanville19Natasha Christie-Holmes20Samira Mubareka21Scott D. Gray-Owen22John L. Rubinstein23Bebhinn Treanor24Jean-Philippe Julien25Program in Molecular Medicine, The Hospital for Sick Children Research InstituteProgram in Molecular Medicine, The Hospital for Sick Children Research InstituteProgram in Molecular Medicine, The Hospital for Sick Children Research InstituteProgram in Molecular Medicine, The Hospital for Sick Children Research InstituteProgram in Molecular Medicine, The Hospital for Sick Children Research InstituteDepartment of Immunology, University of TorontoProgram in Molecular Medicine, The Hospital for Sick Children Research InstituteCombined Containment Level 3 Unit, University of TorontoCombined Containment Level 3 Unit, University of TorontoProgram in Molecular Medicine, The Hospital for Sick Children Research InstituteProgram in Molecular Medicine, The Hospital for Sick Children Research InstituteProgram in Molecular Medicine, The Hospital for Sick Children Research InstituteProgram in Molecular Medicine, The Hospital for Sick Children Research InstituteProgram in Molecular Medicine, The Hospital for Sick Children Research InstituteProgram in Molecular Medicine, The Hospital for Sick Children Research InstituteProgram in Molecular Medicine, The Hospital for Sick Children Research InstituteProgram in Molecular Medicine, The Hospital for Sick Children Research InstituteDistributed BioDistributed BioDistributed BioCombined Containment Level 3 Unit, University of TorontoDepartment of Laboratory Medicine and Pathobiology, University of TorontoDepartment of Molecular Genetics, University of TorontoProgram in Molecular Medicine, The Hospital for Sick Children Research InstituteDepartment of Immunology, University of TorontoProgram in Molecular Medicine, The Hospital for Sick Children Research InstituteHere, the authors combine three different antibody specificities and an Fc domain on a single multivalent molecule, resulting in high neutralization activity despite viral sequence variability.https://doi.org/10.1038/s41467-021-23825-2
collection DOAJ
language English
format Article
sources DOAJ
author Edurne Rujas
Iga Kucharska
Yong Zi Tan
Samir Benlekbir
Hong Cui
Tiantian Zhao
Gregory A. Wasney
Patrick Budylowski
Furkan Guvenc
Jocelyn C. Newton
Taylor Sicard
Anthony Semesi
Krithika Muthuraman
Amy Nouanesengsy
Clare Burn Aschner
Katherine Prieto
Stephanie A. Bueler
Sawsan Youssef
Sindy Liao-Chan
Jacob Glanville
Natasha Christie-Holmes
Samira Mubareka
Scott D. Gray-Owen
John L. Rubinstein
Bebhinn Treanor
Jean-Philippe Julien
spellingShingle Edurne Rujas
Iga Kucharska
Yong Zi Tan
Samir Benlekbir
Hong Cui
Tiantian Zhao
Gregory A. Wasney
Patrick Budylowski
Furkan Guvenc
Jocelyn C. Newton
Taylor Sicard
Anthony Semesi
Krithika Muthuraman
Amy Nouanesengsy
Clare Burn Aschner
Katherine Prieto
Stephanie A. Bueler
Sawsan Youssef
Sindy Liao-Chan
Jacob Glanville
Natasha Christie-Holmes
Samira Mubareka
Scott D. Gray-Owen
John L. Rubinstein
Bebhinn Treanor
Jean-Philippe Julien
Multivalency transforms SARS-CoV-2 antibodies into ultrapotent neutralizers
Nature Communications
author_facet Edurne Rujas
Iga Kucharska
Yong Zi Tan
Samir Benlekbir
Hong Cui
Tiantian Zhao
Gregory A. Wasney
Patrick Budylowski
Furkan Guvenc
Jocelyn C. Newton
Taylor Sicard
Anthony Semesi
Krithika Muthuraman
Amy Nouanesengsy
Clare Burn Aschner
Katherine Prieto
Stephanie A. Bueler
Sawsan Youssef
Sindy Liao-Chan
Jacob Glanville
Natasha Christie-Holmes
Samira Mubareka
Scott D. Gray-Owen
John L. Rubinstein
Bebhinn Treanor
Jean-Philippe Julien
author_sort Edurne Rujas
title Multivalency transforms SARS-CoV-2 antibodies into ultrapotent neutralizers
title_short Multivalency transforms SARS-CoV-2 antibodies into ultrapotent neutralizers
title_full Multivalency transforms SARS-CoV-2 antibodies into ultrapotent neutralizers
title_fullStr Multivalency transforms SARS-CoV-2 antibodies into ultrapotent neutralizers
title_full_unstemmed Multivalency transforms SARS-CoV-2 antibodies into ultrapotent neutralizers
title_sort multivalency transforms sars-cov-2 antibodies into ultrapotent neutralizers
publisher Nature Publishing Group
series Nature Communications
issn 2041-1723
publishDate 2021-06-01
description Here, the authors combine three different antibody specificities and an Fc domain on a single multivalent molecule, resulting in high neutralization activity despite viral sequence variability.
url https://doi.org/10.1038/s41467-021-23825-2
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