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Mutations in an avian IgY-Fc fragment reveal the locations of monocyte Fc receptor binding sites

The avian IgY antibody isotype shares a common ancestor with both mammalian IgG and IgE and so provides a means to study the evolution of their structural and functional specialisations. Although both IgG and IgE bind to their leukocyte Fc receptors with 1:1 stoichiometry, IgY binds to CHIR-AB1, a r...

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Autores principales: Taylor, Alexander I., Sutton, Brian J., Calvert, Rosaleen A.
Formato: Texto
Lenguaje:English
Publicado: Elsevier Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795851/
https://www.ncbi.nlm.nih.gov/pubmed/19733585
http://dx.doi.org/10.1016/j.dci.2009.08.012
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author Taylor, Alexander I.
Sutton, Brian J.
Calvert, Rosaleen A.
author_facet Taylor, Alexander I.
Sutton, Brian J.
Calvert, Rosaleen A.
author_sort Taylor, Alexander I.
collection PubMed
description The avian IgY antibody isotype shares a common ancestor with both mammalian IgG and IgE and so provides a means to study the evolution of their structural and functional specialisations. Although both IgG and IgE bind to their leukocyte Fc receptors with 1:1 stoichiometry, IgY binds to CHIR-AB1, a receptor expressed in avian monocytes, with 2:1 stoichiometry. The mutagenesis data reported here explain the structural basis for this difference, mapping the CHIR-AB1 binding site to the Cυ3/Cυ4 interface and not the N-terminal region of Cυ3 where, at equivalent locations, the IgG and IgE leukocyte Fc receptor binding sites lie. This finding, together with the phylogenetic relationship of the antibodies and their receptors, indicates that a substantial shift in the nature of Fc receptor binding occurred during the evolution of mammalian IgG and IgE.
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spelling pubmed-27958512009-12-22 Mutations in an avian IgY-Fc fragment reveal the locations of monocyte Fc receptor binding sites Taylor, Alexander I. Sutton, Brian J. Calvert, Rosaleen A. Dev Comp Immunol Short Communication The avian IgY antibody isotype shares a common ancestor with both mammalian IgG and IgE and so provides a means to study the evolution of their structural and functional specialisations. Although both IgG and IgE bind to their leukocyte Fc receptors with 1:1 stoichiometry, IgY binds to CHIR-AB1, a receptor expressed in avian monocytes, with 2:1 stoichiometry. The mutagenesis data reported here explain the structural basis for this difference, mapping the CHIR-AB1 binding site to the Cυ3/Cυ4 interface and not the N-terminal region of Cυ3 where, at equivalent locations, the IgG and IgE leukocyte Fc receptor binding sites lie. This finding, together with the phylogenetic relationship of the antibodies and their receptors, indicates that a substantial shift in the nature of Fc receptor binding occurred during the evolution of mammalian IgG and IgE. Elsevier Science 2010-02 /pmc/articles/PMC2795851/ /pubmed/19733585 http://dx.doi.org/10.1016/j.dci.2009.08.012 Text en © 2010 Elsevier Ltd. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Short Communication
Taylor, Alexander I.
Sutton, Brian J.
Calvert, Rosaleen A.
Mutations in an avian IgY-Fc fragment reveal the locations of monocyte Fc receptor binding sites
title Mutations in an avian IgY-Fc fragment reveal the locations of monocyte Fc receptor binding sites
title_full Mutations in an avian IgY-Fc fragment reveal the locations of monocyte Fc receptor binding sites
title_fullStr Mutations in an avian IgY-Fc fragment reveal the locations of monocyte Fc receptor binding sites
title_full_unstemmed Mutations in an avian IgY-Fc fragment reveal the locations of monocyte Fc receptor binding sites
title_short Mutations in an avian IgY-Fc fragment reveal the locations of monocyte Fc receptor binding sites
title_sort mutations in an avian igy-fc fragment reveal the locations of monocyte fc receptor binding sites
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795851/
https://www.ncbi.nlm.nih.gov/pubmed/19733585
http://dx.doi.org/10.1016/j.dci.2009.08.012
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