Insights from native mass spectrometry and ion mobility-mass spectrometry for antibody and antibody-based product characterization.
Fiche publication
Date publication
octobre 2016
Journal
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
Auteurs
Membres identifiés du Cancéropôle Est :
Dr CIANFERANI Sarah
Tous les auteurs :
Terral G, Beck A, Cianférani S
Lien Pubmed
Résumé
Over the past 15 years, monoclonal antibodies (mAbs) have emerged as the most successful class of therapeutics. Their specific structural and functional properties make them highly effective treatments for various diseases. Most therapeutic mAbs are based on chimeric, humanized or human G immunoglobulins (IgGs) selected from three isotypes (1, 2 and 4). IgGs are large and highly complex multimeric glycoproteins. They are constituted of a mixture of isoforms including macro and micro-variants that must be extensively characterized prior to their investigation as a drug candidate in clinical trials. The IgG backbone is also used to design more potent but also more complex biopharmaceuticals such as antibody-drug conjugates, bispecific antibodies, Fc-fusion proteins, and antibody mixtures to name a few. Mass spectrometric approaches in combination with electrophoretic and chromatographic separation methods play a central role in the analytical and structural multi-level (top, middle and bottom) characterization of these compounds. Importantly, techniques allowing the characterization of intact mAbs and related products under non-denaturing conditions are attracting increasing interest. Here, we review the current state of the art in native mass spectrometry and ion mobility methods for the characterization of mAbs and mAb-based products.
Mots clés
Animals, Antibodies, Bispecific, chemistry, Antibodies, Monoclonal, chemistry, Equipment Design, Humans, Immunoconjugates, chemistry, Immunoglobulin G, chemistry, Ions, chemistry, Mass Spectrometry, instrumentation
Référence
J. Chromatogr. B Analyt. Technol. Biomed. Life Sci.. 2016 Oct;1032:79-90