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mD-UPLC-MS/MS: Next Generation of mAb Characterization by Multidimensional Ultraperformance Liquid Chromatography-Mass Spectrometry and Parallel On-Column LysC and Trypsin Digestion
[Image: see text] For the past few years, multidimensional liquid chromatography-mass spectrometry (LC-MS) systems have been commonly used to characterize post-translational modifications (PTMs) of therapeutic antibodies (mAbs). In most cases, this is performed by fractionation of charge variants by...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201819/ https://www.ncbi.nlm.nih.gov/pubmed/35545869 http://dx.doi.org/10.1021/acs.analchem.1c04450 |
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author | Oezipek, Saban Hoelterhoff, Sina Breuer, Simon Bell, Christian Bathke, Anja |
author_facet | Oezipek, Saban Hoelterhoff, Sina Breuer, Simon Bell, Christian Bathke, Anja |
author_sort | Oezipek, Saban |
collection | PubMed |
description | [Image: see text] For the past few years, multidimensional liquid chromatography-mass spectrometry (LC-MS) systems have been commonly used to characterize post-translational modifications (PTMs) of therapeutic antibodies (mAbs). In most cases, this is performed by fractionation of charge variants by ion-exchange chromatography and subsequent online LC-MS peptide mapping analysis. In this study, we developed a multidimensional ultra-performance-liquid-chromatography-mass spectrometry system (mD-UPLC-MS/MS) for PTM characterization and quantification, allowing both rapid analysis and decreased risk of artificial modifications during sample preparation. We implemented UPLC columns for peptide mapping analysis, facilitating the linkage between mD-LC and routine LC-MS workflows. Furthermore, the introduced system incorporates a novel in-parallel trypsin and LysC on-column digestion setup, followed by a combined peptide mapping analysis. This parallel digestion with different enzymes enhances characterization by generating two distinct peptides. Using this approach, a low retentive ethylene oxide adduct of a bispecific antibody was successfully characterized within this study. In summary, our approach allows versatile and rapid analysis of PTMs, enabling efficient characterization of therapeutic molecules. |
format | Online Article Text |
id | pubmed-9201819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-92018192022-06-17 mD-UPLC-MS/MS: Next Generation of mAb Characterization by Multidimensional Ultraperformance Liquid Chromatography-Mass Spectrometry and Parallel On-Column LysC and Trypsin Digestion Oezipek, Saban Hoelterhoff, Sina Breuer, Simon Bell, Christian Bathke, Anja Anal Chem [Image: see text] For the past few years, multidimensional liquid chromatography-mass spectrometry (LC-MS) systems have been commonly used to characterize post-translational modifications (PTMs) of therapeutic antibodies (mAbs). In most cases, this is performed by fractionation of charge variants by ion-exchange chromatography and subsequent online LC-MS peptide mapping analysis. In this study, we developed a multidimensional ultra-performance-liquid-chromatography-mass spectrometry system (mD-UPLC-MS/MS) for PTM characterization and quantification, allowing both rapid analysis and decreased risk of artificial modifications during sample preparation. We implemented UPLC columns for peptide mapping analysis, facilitating the linkage between mD-LC and routine LC-MS workflows. Furthermore, the introduced system incorporates a novel in-parallel trypsin and LysC on-column digestion setup, followed by a combined peptide mapping analysis. This parallel digestion with different enzymes enhances characterization by generating two distinct peptides. Using this approach, a low retentive ethylene oxide adduct of a bispecific antibody was successfully characterized within this study. In summary, our approach allows versatile and rapid analysis of PTMs, enabling efficient characterization of therapeutic molecules. American Chemical Society 2022-05-12 2022-06-14 /pmc/articles/PMC9201819/ /pubmed/35545869 http://dx.doi.org/10.1021/acs.analchem.1c04450 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Oezipek, Saban Hoelterhoff, Sina Breuer, Simon Bell, Christian Bathke, Anja mD-UPLC-MS/MS: Next Generation of mAb Characterization by Multidimensional Ultraperformance Liquid Chromatography-Mass Spectrometry and Parallel On-Column LysC and Trypsin Digestion |
title | mD-UPLC-MS/MS: Next Generation of mAb Characterization
by Multidimensional Ultraperformance Liquid Chromatography-Mass Spectrometry
and Parallel On-Column LysC and Trypsin Digestion |
title_full | mD-UPLC-MS/MS: Next Generation of mAb Characterization
by Multidimensional Ultraperformance Liquid Chromatography-Mass Spectrometry
and Parallel On-Column LysC and Trypsin Digestion |
title_fullStr | mD-UPLC-MS/MS: Next Generation of mAb Characterization
by Multidimensional Ultraperformance Liquid Chromatography-Mass Spectrometry
and Parallel On-Column LysC and Trypsin Digestion |
title_full_unstemmed | mD-UPLC-MS/MS: Next Generation of mAb Characterization
by Multidimensional Ultraperformance Liquid Chromatography-Mass Spectrometry
and Parallel On-Column LysC and Trypsin Digestion |
title_short | mD-UPLC-MS/MS: Next Generation of mAb Characterization
by Multidimensional Ultraperformance Liquid Chromatography-Mass Spectrometry
and Parallel On-Column LysC and Trypsin Digestion |
title_sort | md-uplc-ms/ms: next generation of mab characterization
by multidimensional ultraperformance liquid chromatography-mass spectrometry
and parallel on-column lysc and trypsin digestion |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201819/ https://www.ncbi.nlm.nih.gov/pubmed/35545869 http://dx.doi.org/10.1021/acs.analchem.1c04450 |
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