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Conformational Correction Mechanisms Aiding Antigen Recognition by a Humanized Antibody

The crystal structure of the complex between hen egg lysozyme and the Fv fragment of a humanized antilysozyme antibody was determined to 2.7-Å resolution. The structure of the antigen combining site in the complex is nearly identical to that of the complexed form of the parent mouse antibody, D1.3....

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Detalles Bibliográficos
Autores principales: Holmes, Margaret A., Buss, Timothy N., Foote, Jefferson
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1998
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2212146/
https://www.ncbi.nlm.nih.gov/pubmed/9463398
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author Holmes, Margaret A.
Buss, Timothy N.
Foote, Jefferson
author_facet Holmes, Margaret A.
Buss, Timothy N.
Foote, Jefferson
author_sort Holmes, Margaret A.
collection PubMed
description The crystal structure of the complex between hen egg lysozyme and the Fv fragment of a humanized antilysozyme antibody was determined to 2.7-Å resolution. The structure of the antigen combining site in the complex is nearly identical to that of the complexed form of the parent mouse antibody, D1.3. In contrast, the combining sites of the unliganded mouse and humanized antilysozymes show moderate conformational differences. This disparity suggests that a conformational readjustment process linked to antigen binding reverses adverse conformations in the complementarity determining regions that had been introduced by engineering these segments next to human framework regions in the humanized antibody.
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spelling pubmed-22121462008-04-22 Conformational Correction Mechanisms Aiding Antigen Recognition by a Humanized Antibody Holmes, Margaret A. Buss, Timothy N. Foote, Jefferson J Exp Med Article The crystal structure of the complex between hen egg lysozyme and the Fv fragment of a humanized antilysozyme antibody was determined to 2.7-Å resolution. The structure of the antigen combining site in the complex is nearly identical to that of the complexed form of the parent mouse antibody, D1.3. In contrast, the combining sites of the unliganded mouse and humanized antilysozymes show moderate conformational differences. This disparity suggests that a conformational readjustment process linked to antigen binding reverses adverse conformations in the complementarity determining regions that had been introduced by engineering these segments next to human framework regions in the humanized antibody. The Rockefeller University Press 1998-02-16 /pmc/articles/PMC2212146/ /pubmed/9463398 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Holmes, Margaret A.
Buss, Timothy N.
Foote, Jefferson
Conformational Correction Mechanisms Aiding Antigen Recognition by a Humanized Antibody
title Conformational Correction Mechanisms Aiding Antigen Recognition by a Humanized Antibody
title_full Conformational Correction Mechanisms Aiding Antigen Recognition by a Humanized Antibody
title_fullStr Conformational Correction Mechanisms Aiding Antigen Recognition by a Humanized Antibody
title_full_unstemmed Conformational Correction Mechanisms Aiding Antigen Recognition by a Humanized Antibody
title_short Conformational Correction Mechanisms Aiding Antigen Recognition by a Humanized Antibody
title_sort conformational correction mechanisms aiding antigen recognition by a humanized antibody
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2212146/
https://www.ncbi.nlm.nih.gov/pubmed/9463398
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