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author Dacon, Cherrelle
Tucker, Courtney
Peng, Linghang
Lee, Chang-Chun D.
Lin, Ting-Hui
Yuan, Meng
Cong, Yu
Wang, Lingshu
Purser, Lauren
Williams, Jazmean K.
Pyo, Chul-Woo
Kosik, Ivan
Hu, Zhe
Zhao, Ming
Mohan, Divya
Cooper, Andrew J. R.
Peterson, Mary
Skinner, Jeff
Dixit, Saurabh
Kollins, Erin
Huzella, Louis
Perry, Donna
Byrum, Russell
Lembirik, Sanae
Drawbaugh, David
Eaton, Brett
Zhang, Yi
Yang, Eun Sung
Chen, Man
Leung, Kwanyee
Weinberg, Rona S.
Pegu, Amarendra
Geraghty, Daniel E.
Davidson, Edgar
Douagi, Iyadh
Moir, Susan
Yewdell, Jonathan W.
Schmaljohn, Connie
Crompton, Peter D.
Holbrook, Michael R.
Nemazee, David
Mascola, John R.
Wilson, Ian A.
Tan, Joshua
author_facet Dacon, Cherrelle
Tucker, Courtney
Peng, Linghang
Lee, Chang-Chun D.
Lin, Ting-Hui
Yuan, Meng
Cong, Yu
Wang, Lingshu
Purser, Lauren
Williams, Jazmean K.
Pyo, Chul-Woo
Kosik, Ivan
Hu, Zhe
Zhao, Ming
Mohan, Divya
Cooper, Andrew J. R.
Peterson, Mary
Skinner, Jeff
Dixit, Saurabh
Kollins, Erin
Huzella, Louis
Perry, Donna
Byrum, Russell
Lembirik, Sanae
Drawbaugh, David
Eaton, Brett
Zhang, Yi
Yang, Eun Sung
Chen, Man
Leung, Kwanyee
Weinberg, Rona S.
Pegu, Amarendra
Geraghty, Daniel E.
Davidson, Edgar
Douagi, Iyadh
Moir, Susan
Yewdell, Jonathan W.
Schmaljohn, Connie
Crompton, Peter D.
Holbrook, Michael R.
Nemazee, David
Mascola, John R.
Wilson, Ian A.
Tan, Joshua
author_sort Dacon, Cherrelle
collection PubMed
description The potential for future coronavirus outbreaks highlights the need to broadly target this group of pathogens. We use an epitope-agnostic approach to identify six monoclonal antibodies that bind to spike proteins from all seven human-infecting coronaviruses. All six antibodies target the conserved fusion peptide region adjacent to the S2' cleavage site. COV44-62 and COV44-79 broadly neutralize alpha and beta coronaviruses, including SARS-CoV-2 Omicron subvariants BA.2 and BA.4/5, albeit with lower potency than RBD-specific antibodies. In crystal structures of Fabs COV44-62 and COV44-79 with the SARS-CoV-2 fusion peptide, the fusion peptide epitope adopts a helical structure and includes the arginine at the S2' cleavage site. COV44-79 limited disease caused by SARS-CoV-2 in a Syrian hamster model. These findings highlight the fusion peptide as a candidate epitope for next-generation coronavirus vaccine development.
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spelling pubmed-93487542022-08-05 Broadly neutralizing antibodies target the coronavirus fusion peptide Dacon, Cherrelle Tucker, Courtney Peng, Linghang Lee, Chang-Chun D. Lin, Ting-Hui Yuan, Meng Cong, Yu Wang, Lingshu Purser, Lauren Williams, Jazmean K. Pyo, Chul-Woo Kosik, Ivan Hu, Zhe Zhao, Ming Mohan, Divya Cooper, Andrew J. R. Peterson, Mary Skinner, Jeff Dixit, Saurabh Kollins, Erin Huzella, Louis Perry, Donna Byrum, Russell Lembirik, Sanae Drawbaugh, David Eaton, Brett Zhang, Yi Yang, Eun Sung Chen, Man Leung, Kwanyee Weinberg, Rona S. Pegu, Amarendra Geraghty, Daniel E. Davidson, Edgar Douagi, Iyadh Moir, Susan Yewdell, Jonathan W. Schmaljohn, Connie Crompton, Peter D. Holbrook, Michael R. Nemazee, David Mascola, John R. Wilson, Ian A. Tan, Joshua Science Research Articles The potential for future coronavirus outbreaks highlights the need to broadly target this group of pathogens. We use an epitope-agnostic approach to identify six monoclonal antibodies that bind to spike proteins from all seven human-infecting coronaviruses. All six antibodies target the conserved fusion peptide region adjacent to the S2' cleavage site. COV44-62 and COV44-79 broadly neutralize alpha and beta coronaviruses, including SARS-CoV-2 Omicron subvariants BA.2 and BA.4/5, albeit with lower potency than RBD-specific antibodies. In crystal structures of Fabs COV44-62 and COV44-79 with the SARS-CoV-2 fusion peptide, the fusion peptide epitope adopts a helical structure and includes the arginine at the S2' cleavage site. COV44-79 limited disease caused by SARS-CoV-2 in a Syrian hamster model. These findings highlight the fusion peptide as a candidate epitope for next-generation coronavirus vaccine development. American Association for the Advancement of Science 2022-07-12 /pmc/articles/PMC9348754/ /pubmed/35857439 http://dx.doi.org/10.1126/science.abq3773 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Dacon, Cherrelle
Tucker, Courtney
Peng, Linghang
Lee, Chang-Chun D.
Lin, Ting-Hui
Yuan, Meng
Cong, Yu
Wang, Lingshu
Purser, Lauren
Williams, Jazmean K.
Pyo, Chul-Woo
Kosik, Ivan
Hu, Zhe
Zhao, Ming
Mohan, Divya
Cooper, Andrew J. R.
Peterson, Mary
Skinner, Jeff
Dixit, Saurabh
Kollins, Erin
Huzella, Louis
Perry, Donna
Byrum, Russell
Lembirik, Sanae
Drawbaugh, David
Eaton, Brett
Zhang, Yi
Yang, Eun Sung
Chen, Man
Leung, Kwanyee
Weinberg, Rona S.
Pegu, Amarendra
Geraghty, Daniel E.
Davidson, Edgar
Douagi, Iyadh
Moir, Susan
Yewdell, Jonathan W.
Schmaljohn, Connie
Crompton, Peter D.
Holbrook, Michael R.
Nemazee, David
Mascola, John R.
Wilson, Ian A.
Tan, Joshua
Broadly neutralizing antibodies target the coronavirus fusion peptide
title Broadly neutralizing antibodies target the coronavirus fusion peptide
title_full Broadly neutralizing antibodies target the coronavirus fusion peptide
title_fullStr Broadly neutralizing antibodies target the coronavirus fusion peptide
title_full_unstemmed Broadly neutralizing antibodies target the coronavirus fusion peptide
title_short Broadly neutralizing antibodies target the coronavirus fusion peptide
title_sort broadly neutralizing antibodies target the coronavirus fusion peptide
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9348754/
https://www.ncbi.nlm.nih.gov/pubmed/35857439
http://dx.doi.org/10.1126/science.abq3773
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