Role of NMR in High Ordered Structure Characterization of Monoclonal Antibodies
Obtaining high ordered structure (HOS) information is of importance to guarantee the efficacy and safety of monoclonal antibodies (mAbs) in clinical application. Assessment of HOS should ideally be performed in a non-invasive manner under their formulated storage conditions, as any perturbation can...
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description | Obtaining high ordered structure (HOS) information is of importance to guarantee the efficacy and safety of monoclonal antibodies (mAbs) in clinical application. Assessment of HOS should ideally be performed in a non-invasive manner under their formulated storage conditions, as any perturbation can introduce unexpected detritions. However, most of the currently available techniques only indirectly report HOS of mAbs and/or require a certain condition to conduct the analyses. Besides, the flexible multidomain architecture of mAbs has hampered atomic-resolution structural analyses using X-ray crystallography and cryo-electron microscopy. In contrast, the ability of nuclear magnetic resonance (NMR) spectroscopy to structurally analyze biomolecules in various conditions in a non-invasive and quantitative manner is suitable to meet the needs. However, the application of NMR to mAbs is not straightforward due to the high molecular weight of the system. In this review, we will discuss how NMR techniques have been applied to HOS analysis of mAbs, along with the recent advances of the novel
N direct detection NMR strategy that allows for obtaining the structural fingerprint of mAbs at lower temperatures under multiple formulation conditions. The potential application of these NMR strategies will benefit next-generation mAbs, such as antibody-drug conjugates and bispecific antibodies. |
doi_str_mv | 10.3390/ijms22010046 |
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N direct detection NMR strategy that allows for obtaining the structural fingerprint of mAbs at lower temperatures under multiple formulation conditions. 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N direct detection NMR strategy that allows for obtaining the structural fingerprint of mAbs at lower temperatures under multiple formulation conditions. The potential application of these NMR strategies will benefit next-generation mAbs, such as antibody-drug conjugates and bispecific antibodies.</abstract><cop>Switzerland</cop><pub>MDPI</pub><pmid>33375207</pmid><doi>10.3390/ijms22010046</doi><orcidid>https://orcid.org/0000-0002-6227-4627</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies, Monoclonal - chemistry Antibodies, Monoclonal - metabolism Antibodies, Monoclonal - ultrastructure Cryoelectron Microscopy Crystallography, X-Ray Glycosylation Immunoglobulin Fc Fragments - chemistry Immunoglobulin Fc Fragments - metabolism Immunoglobulin Fc Fragments - ultrastructure Immunoglobulin G - chemistry Immunoglobulin G - metabolism Immunoglobulin G - ultrastructure Magnetic Resonance Spectroscopy - methods Models, Molecular Protein Conformation Protein Stability Review |
title | Role of NMR in High Ordered Structure Characterization of Monoclonal Antibodies |
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