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Glycoform-resolved FcɣRIIIa affinity chromatography–mass spectrometry
Determination of the impact of individual antibody glycoforms on FcɣRIIIa affinity, and consequently antibody-dependent cell-mediated cytotoxicity (ADCC) previously required high purity glycoengineering. We hyphenated FcɣRIIIa affinity chromatography to mass spectrometry, which allowed direct affini...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6748599/ https://www.ncbi.nlm.nih.gov/pubmed/31276431 http://dx.doi.org/10.1080/19420862.2019.1636602 |
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author | Lippold, Steffen Nicolardi, Simone Domínguez-Vega, Elena Heidenreich, Anna-Katharina Vidarsson, Gestur Reusch, Dietmar Haberger, Markus Wuhrer, Manfred Falck, David |
author_facet | Lippold, Steffen Nicolardi, Simone Domínguez-Vega, Elena Heidenreich, Anna-Katharina Vidarsson, Gestur Reusch, Dietmar Haberger, Markus Wuhrer, Manfred Falck, David |
author_sort | Lippold, Steffen |
collection | PubMed |
description | Determination of the impact of individual antibody glycoforms on FcɣRIIIa affinity, and consequently antibody-dependent cell-mediated cytotoxicity (ADCC) previously required high purity glycoengineering. We hyphenated FcɣRIIIa affinity chromatography to mass spectrometry, which allowed direct affinity comparison of glycoforms of intact monoclonal antibodies. The approach enabled reproduction and refinement of known glycosylation effects, and insights on afucosylation pairing as well as on low-abundant, unstudied glycoforms. Our method greatly improves the understanding of individual glycoform structure–function relationships. Thus, it is highly relevant for assessing Fc-glycosylation critical quality attributes related to ADCC. |
format | Online Article Text |
id | pubmed-6748599 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-67485992019-09-25 Glycoform-resolved FcɣRIIIa affinity chromatography–mass spectrometry Lippold, Steffen Nicolardi, Simone Domínguez-Vega, Elena Heidenreich, Anna-Katharina Vidarsson, Gestur Reusch, Dietmar Haberger, Markus Wuhrer, Manfred Falck, David MAbs Short Communication Determination of the impact of individual antibody glycoforms on FcɣRIIIa affinity, and consequently antibody-dependent cell-mediated cytotoxicity (ADCC) previously required high purity glycoengineering. We hyphenated FcɣRIIIa affinity chromatography to mass spectrometry, which allowed direct affinity comparison of glycoforms of intact monoclonal antibodies. The approach enabled reproduction and refinement of known glycosylation effects, and insights on afucosylation pairing as well as on low-abundant, unstudied glycoforms. Our method greatly improves the understanding of individual glycoform structure–function relationships. Thus, it is highly relevant for assessing Fc-glycosylation critical quality attributes related to ADCC. Taylor & Francis 2019-08-02 /pmc/articles/PMC6748599/ /pubmed/31276431 http://dx.doi.org/10.1080/19420862.2019.1636602 Text en © 2019 The Author(s). Published with license by Taylor & Francis Group, LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Short Communication Lippold, Steffen Nicolardi, Simone Domínguez-Vega, Elena Heidenreich, Anna-Katharina Vidarsson, Gestur Reusch, Dietmar Haberger, Markus Wuhrer, Manfred Falck, David Glycoform-resolved FcɣRIIIa affinity chromatography–mass spectrometry |
title | Glycoform-resolved FcɣRIIIa affinity chromatography–mass spectrometry |
title_full | Glycoform-resolved FcɣRIIIa affinity chromatography–mass spectrometry |
title_fullStr | Glycoform-resolved FcɣRIIIa affinity chromatography–mass spectrometry |
title_full_unstemmed | Glycoform-resolved FcɣRIIIa affinity chromatography–mass spectrometry |
title_short | Glycoform-resolved FcɣRIIIa affinity chromatography–mass spectrometry |
title_sort | glycoform-resolved fcɣriiia affinity chromatography–mass spectrometry |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6748599/ https://www.ncbi.nlm.nih.gov/pubmed/31276431 http://dx.doi.org/10.1080/19420862.2019.1636602 |
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