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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...

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Detalles Bibliográficos
Autores principales: Lippold, Steffen, Nicolardi, Simone, Domínguez-Vega, Elena, Heidenreich, Anna-Katharina, Vidarsson, Gestur, Reusch, Dietmar, Haberger, Markus, Wuhrer, Manfred, Falck, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
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
Descripción
Sumario: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.