Human neutralizing antibodies to cold linear epitopes and subdomain 1 of the SARS-CoV-2 spike glycoprotein
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem, Research Support, N.I.H., Extramural
Grantová podpora
P30 GM133894
NIGMS NIH HHS - United States
P01 AI138938
NIAID NIH HHS - United States
196866
Swiss National Science Foundation - Switzerland
U19 AI111825
NIAID NIH HHS - United States
U01 AI151698
NIAID NIH HHS - United States
PubMed
36701425
PubMed Central
PMC9972897
DOI
10.1126/sciimmunol.ade0958
Knihovny.cz E-zdroje
- MeSH
- COVID-19 * MeSH
- epitopy MeSH
- glykoprotein S, koronavirus MeSH
- lidé MeSH
- myši MeSH
- neutralizační testy MeSH
- neutralizující protilátky * MeSH
- protilátky virové MeSH
- SARS-CoV-2 MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- epitopy MeSH
- glykoprotein S, koronavirus MeSH
- neutralizující protilátky * MeSH
- protilátky virové MeSH
- spike protein, SARS-CoV-2 MeSH Prohlížeč
Emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants diminishes the efficacy of vaccines and antiviral monoclonal antibodies. Continued development of immunotherapies and vaccine immunogens resilient to viral evolution is therefore necessary. Using coldspot-guided antibody discovery, a screening approach that focuses on portions of the virus spike glycoprotein that are both functionally relevant and averse to change, we identified human neutralizing antibodies to highly conserved viral epitopes. Antibody fp.006 binds the fusion peptide and cross-reacts against coronaviruses of the four genera, including the nine human coronaviruses, through recognition of a conserved motif that includes the S2' site of proteolytic cleavage. Antibody hr2.016 targets the stem helix and neutralizes SARS-CoV-2 variants. Antibody sd1.040 binds to subdomain 1, synergizes with antibody rbd.042 for neutralization, and, similar to fp.006 and hr2.016, protects mice expressing human angiotensin-converting enzyme 2 against infection when present as a bispecific antibody. Thus, coldspot-guided antibody discovery reveals donor-derived neutralizing antibodies that are cross-reactive with Orthocoronavirinae, including SARS-CoV-2 variants.
Chan Zuckerberg Biohub San Francisco CA USA
Clinical Research Unit Clinica Luganese Moncucco Lugano Switzerland
Department of Biology Stanford University Stanford CA USA
Department of Biosciences and Nutrition Karolinska Institutet Huddinge Sweden
Department of Chemistry and Biochemistry Mendel University in Brno Brno Czech Republic
Department of Clinical Surgical Diagnostic and Pediatric Sciences University of Pavia Pavia Italy
Department of Experimental Biology Faculty of Science Masaryk University Brno Czech Republic
European Commission Joint Research Centre Ispra Italy
Faculty of Science University of South Bohemia Ceske Budejovice Czech Republic
Institute for Research in Biomedicine Università della Svizzera italiana Bellinzona Switzerland
Internal Medicine and Infectious Diseases Clinica Luganese Moncucco Lugano Switzerland
Microbiology and Virology Department Fondazione IRCCS Policlinico San Matteo Pavia Italy
Sarafan ChEM H Macromolecular Structure Knowledge Center Stanford University Stanford CA USA
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