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Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases
Using a comprehensive set of discovery and optimization tools, antibodies were produced with the ability to neutralize SARS coronavirus (SARS-CoV) infection in Vero E6 cells and in animal models. These anti-SARS antibodies were discovered using a novel DNA display method, which can identify new anti...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2461042/ https://www.ncbi.nlm.nih.gov/pubmed/18480090 http://dx.doi.org/10.1093/protein/gzn027 |
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author | Rogers, J. Schoepp, R.J. Schröder, O. Clements, T.L. Holland, T.F. Li, J.Q. Li, J. Lewis, L.M. Dirmeier, R.P. Frey, G.J. Tan, X. Wong, K. Woodnutt, G. Keller, M. Reed, D.S. Kimmel, B.E. Tozer, E.C. |
author_facet | Rogers, J. Schoepp, R.J. Schröder, O. Clements, T.L. Holland, T.F. Li, J.Q. Li, J. Lewis, L.M. Dirmeier, R.P. Frey, G.J. Tan, X. Wong, K. Woodnutt, G. Keller, M. Reed, D.S. Kimmel, B.E. Tozer, E.C. |
author_sort | Rogers, J. |
collection | PubMed |
description | Using a comprehensive set of discovery and optimization tools, antibodies were produced with the ability to neutralize SARS coronavirus (SARS-CoV) infection in Vero E6 cells and in animal models. These anti-SARS antibodies were discovered using a novel DNA display method, which can identify new antibodies within days. Once neutralizing antibodies were identified, a comprehensive and effective means of converting the mouse sequences to human frameworks was accomplished using HuFR™ (human framework reassembly) technology. The best variant (61G4) from this screen showed a 3.5–4-fold improvement in neutralization of SARS-CoV infection in vitro. Finally, using a complete site-saturation mutagenesis methodology focused on the CDR (complementarity determining regions), a single point mutation (51E7) was identified that improved the 80% plaque reduction neutralization of the virus by greater than 8-fold. These discovery and evolution strategies can be applied to any emerging pathogen or toxin where a causative agent is known. |
format | Text |
id | pubmed-2461042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-24610422009-02-25 Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases Rogers, J. Schoepp, R.J. Schröder, O. Clements, T.L. Holland, T.F. Li, J.Q. Li, J. Lewis, L.M. Dirmeier, R.P. Frey, G.J. Tan, X. Wong, K. Woodnutt, G. Keller, M. Reed, D.S. Kimmel, B.E. Tozer, E.C. Protein Eng Des Sel Original Articles Using a comprehensive set of discovery and optimization tools, antibodies were produced with the ability to neutralize SARS coronavirus (SARS-CoV) infection in Vero E6 cells and in animal models. These anti-SARS antibodies were discovered using a novel DNA display method, which can identify new antibodies within days. Once neutralizing antibodies were identified, a comprehensive and effective means of converting the mouse sequences to human frameworks was accomplished using HuFR™ (human framework reassembly) technology. The best variant (61G4) from this screen showed a 3.5–4-fold improvement in neutralization of SARS-CoV infection in vitro. Finally, using a complete site-saturation mutagenesis methodology focused on the CDR (complementarity determining regions), a single point mutation (51E7) was identified that improved the 80% plaque reduction neutralization of the virus by greater than 8-fold. These discovery and evolution strategies can be applied to any emerging pathogen or toxin where a causative agent is known. Oxford University Press 2008-08 2008-05-13 /pmc/articles/PMC2461042/ /pubmed/18480090 http://dx.doi.org/10.1093/protein/gzn027 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Rogers, J. Schoepp, R.J. Schröder, O. Clements, T.L. Holland, T.F. Li, J.Q. Li, J. Lewis, L.M. Dirmeier, R.P. Frey, G.J. Tan, X. Wong, K. Woodnutt, G. Keller, M. Reed, D.S. Kimmel, B.E. Tozer, E.C. Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases |
title | Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases |
title_full | Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases |
title_fullStr | Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases |
title_full_unstemmed | Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases |
title_short | Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases |
title_sort | rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2461042/ https://www.ncbi.nlm.nih.gov/pubmed/18480090 http://dx.doi.org/10.1093/protein/gzn027 |
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