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Identification of novel antibody-reactive detection sites for comprehensive gluten monitoring

Certain cereals like wheat, rye or barley contain gluten, a protein mixture that can trigger celiac disease (CD). To make gluten-free diets available for affected individuals the gluten content of foodstuff must be monitored. For this purpose, antibody-based assays exist which rely on the recognitio...

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Autores principales: Röckendorf, Niels, Meckelein, Barbara, Scherf, Katharina A., Schalk, Kathrin, Koehler, Peter, Frey, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536345/
https://www.ncbi.nlm.nih.gov/pubmed/28759621
http://dx.doi.org/10.1371/journal.pone.0181566
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author Röckendorf, Niels
Meckelein, Barbara
Scherf, Katharina A.
Schalk, Kathrin
Koehler, Peter
Frey, Andreas
author_facet Röckendorf, Niels
Meckelein, Barbara
Scherf, Katharina A.
Schalk, Kathrin
Koehler, Peter
Frey, Andreas
author_sort Röckendorf, Niels
collection PubMed
description Certain cereals like wheat, rye or barley contain gluten, a protein mixture that can trigger celiac disease (CD). To make gluten-free diets available for affected individuals the gluten content of foodstuff must be monitored. For this purpose, antibody-based assays exist which rely on the recognition of certain linear gluten sequence motifs. Yet, not all CD-active gluten constituents and fragments formed during food processing/fermentation may be covered by those tests. In this study, we therefore assayed the coverage of reportedly CD-active gluten components by currently available detection antibodies and determined the antibody-inducing capacity of wheat gluten constituents in order to provide novel diagnostic targets for comprehensive gluten quantitation. Immunizations of outbred mice with purified gliadins and glutenins were conducted and the linear target recognition profile of the sera was recorded using synthetic peptide arrays that covered the sequence space of gluten constituents present in those preparations. The resulting murine immunorecognition profile of gluten demonstrated that further linear binding sites beyond those recognized by the monoclonal antibodies α20, R5 and G12 exist and may be exploitable as diagnostic targets. We conclude that the safety of foodstuffs for CD patients can be further improved by complementing current tests with antibodies directed against additional CD-active gluten components. Currently unrepresented linear gluten detection sites in glutenins and α-gliadins suggest sequences QQQYPS, PQQSFP, QPGQGQQG and QQPPFS as novel targets for antibody generation.
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spelling pubmed-55363452017-08-07 Identification of novel antibody-reactive detection sites for comprehensive gluten monitoring Röckendorf, Niels Meckelein, Barbara Scherf, Katharina A. Schalk, Kathrin Koehler, Peter Frey, Andreas PLoS One Research Article Certain cereals like wheat, rye or barley contain gluten, a protein mixture that can trigger celiac disease (CD). To make gluten-free diets available for affected individuals the gluten content of foodstuff must be monitored. For this purpose, antibody-based assays exist which rely on the recognition of certain linear gluten sequence motifs. Yet, not all CD-active gluten constituents and fragments formed during food processing/fermentation may be covered by those tests. In this study, we therefore assayed the coverage of reportedly CD-active gluten components by currently available detection antibodies and determined the antibody-inducing capacity of wheat gluten constituents in order to provide novel diagnostic targets for comprehensive gluten quantitation. Immunizations of outbred mice with purified gliadins and glutenins were conducted and the linear target recognition profile of the sera was recorded using synthetic peptide arrays that covered the sequence space of gluten constituents present in those preparations. The resulting murine immunorecognition profile of gluten demonstrated that further linear binding sites beyond those recognized by the monoclonal antibodies α20, R5 and G12 exist and may be exploitable as diagnostic targets. We conclude that the safety of foodstuffs for CD patients can be further improved by complementing current tests with antibodies directed against additional CD-active gluten components. Currently unrepresented linear gluten detection sites in glutenins and α-gliadins suggest sequences QQQYPS, PQQSFP, QPGQGQQG and QQPPFS as novel targets for antibody generation. Public Library of Science 2017-07-31 /pmc/articles/PMC5536345/ /pubmed/28759621 http://dx.doi.org/10.1371/journal.pone.0181566 Text en © 2017 Röckendorf et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Röckendorf, Niels
Meckelein, Barbara
Scherf, Katharina A.
Schalk, Kathrin
Koehler, Peter
Frey, Andreas
Identification of novel antibody-reactive detection sites for comprehensive gluten monitoring
title Identification of novel antibody-reactive detection sites for comprehensive gluten monitoring
title_full Identification of novel antibody-reactive detection sites for comprehensive gluten monitoring
title_fullStr Identification of novel antibody-reactive detection sites for comprehensive gluten monitoring
title_full_unstemmed Identification of novel antibody-reactive detection sites for comprehensive gluten monitoring
title_short Identification of novel antibody-reactive detection sites for comprehensive gluten monitoring
title_sort identification of novel antibody-reactive detection sites for comprehensive gluten monitoring
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536345/
https://www.ncbi.nlm.nih.gov/pubmed/28759621
http://dx.doi.org/10.1371/journal.pone.0181566
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