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Mechanisms of Neutralization of a Human Anti-α-toxin Antibody

MEDI4893 is a neutralizing human monoclonal antibody that targets α-toxin (AT) and is currently undergoing evaluation in the field of Staphylococcus aureus-mediated diseases. We have solved the crystal structure of MEDI4893 Fab bound to monomeric AT at a resolution of 2.56 Å and further characterize...

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Autores principales: Oganesyan, Vaheh, Peng, Li, Damschroder, Melissa M., Cheng, Li, Sadowska, Agnieszka, Tkaczyk, Christine, Sellman, Bret R., Wu, Herren, Dall'Acqua, William F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207998/
https://www.ncbi.nlm.nih.gov/pubmed/25210036
http://dx.doi.org/10.1074/jbc.M114.601328
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author Oganesyan, Vaheh
Peng, Li
Damschroder, Melissa M.
Cheng, Li
Sadowska, Agnieszka
Tkaczyk, Christine
Sellman, Bret R.
Wu, Herren
Dall'Acqua, William F.
author_facet Oganesyan, Vaheh
Peng, Li
Damschroder, Melissa M.
Cheng, Li
Sadowska, Agnieszka
Tkaczyk, Christine
Sellman, Bret R.
Wu, Herren
Dall'Acqua, William F.
author_sort Oganesyan, Vaheh
collection PubMed
description MEDI4893 is a neutralizing human monoclonal antibody that targets α-toxin (AT) and is currently undergoing evaluation in the field of Staphylococcus aureus-mediated diseases. We have solved the crystal structure of MEDI4893 Fab bound to monomeric AT at a resolution of 2.56 Å and further characterized its epitope using various engineered AT variants. We have found that MEDI4893 recognizes a novel epitope in the so-called “rim” domain of AT and exerts its neutralizing effect through a dual mechanism. In particular, MEDI4893 not only sterically blocks binding of AT to its cell receptor but also prevents it from adopting a lytic heptameric trans-membrane conformation.
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spelling pubmed-42079982014-10-27 Mechanisms of Neutralization of a Human Anti-α-toxin Antibody Oganesyan, Vaheh Peng, Li Damschroder, Melissa M. Cheng, Li Sadowska, Agnieszka Tkaczyk, Christine Sellman, Bret R. Wu, Herren Dall'Acqua, William F. J Biol Chem Protein Structure and Folding MEDI4893 is a neutralizing human monoclonal antibody that targets α-toxin (AT) and is currently undergoing evaluation in the field of Staphylococcus aureus-mediated diseases. We have solved the crystal structure of MEDI4893 Fab bound to monomeric AT at a resolution of 2.56 Å and further characterized its epitope using various engineered AT variants. We have found that MEDI4893 recognizes a novel epitope in the so-called “rim” domain of AT and exerts its neutralizing effect through a dual mechanism. In particular, MEDI4893 not only sterically blocks binding of AT to its cell receptor but also prevents it from adopting a lytic heptameric trans-membrane conformation. American Society for Biochemistry and Molecular Biology 2014-10-24 2014-09-10 /pmc/articles/PMC4207998/ /pubmed/25210036 http://dx.doi.org/10.1074/jbc.M114.601328 Text en © 2014 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version full access. Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/) applies to Author Choice Articles
spellingShingle Protein Structure and Folding
Oganesyan, Vaheh
Peng, Li
Damschroder, Melissa M.
Cheng, Li
Sadowska, Agnieszka
Tkaczyk, Christine
Sellman, Bret R.
Wu, Herren
Dall'Acqua, William F.
Mechanisms of Neutralization of a Human Anti-α-toxin Antibody
title Mechanisms of Neutralization of a Human Anti-α-toxin Antibody
title_full Mechanisms of Neutralization of a Human Anti-α-toxin Antibody
title_fullStr Mechanisms of Neutralization of a Human Anti-α-toxin Antibody
title_full_unstemmed Mechanisms of Neutralization of a Human Anti-α-toxin Antibody
title_short Mechanisms of Neutralization of a Human Anti-α-toxin Antibody
title_sort mechanisms of neutralization of a human anti-α-toxin antibody
topic Protein Structure and Folding
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207998/
https://www.ncbi.nlm.nih.gov/pubmed/25210036
http://dx.doi.org/10.1074/jbc.M114.601328
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