Interlaboratory study for characterizing monoclonal antibodies by top-down and middle-down mass spectrometry
| العنوان: | Interlaboratory study for characterizing monoclonal antibodies by top-down and middle-down mass spectrometry |
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| المؤلفون: | Sam Hughes, Nicolas L. Young, David Clarke, Frank Sobott, Anja Resemann, Kristina Srzentić, Kim F. Haselmann, Detlev Suckau, Dina L. Bai, Young Ah Goo, Christian Malosse, Mathieu Dupré, Sylvester M. Greer, Neil R. Quebbemann, Ziqing Lin, Jared B. Shaw, Alain Beck, Yury O. Tsybin, Stuart Pengelley, Timothy K. Toby, Lidong He, Paul O. Danis, Henrique S. Seckler, Robert Anthony D’Ippolito, Natalia Gasilova, Jeffrey N. Agar, Donald F. Hunt, Jennifer S. Brodbelt, Matthew V. Holt, Simone Nicolardi, Joseph A. Loo, Yuri E. M. van der Burgt, Nicholas D. Schmitt, Laure Menin, Robert J. Millikin, Ljiljana Paša-Tolić, David R. Goodlett, Mowei Zhou, Joshua D. Hinkle, Michael R. Shortreed, Christopher L. Hendrickson, Wendy Sandoval, Richa Sarin, Jeffrey Shabanowitz, Alan G. Marshall, Anton N. Kozhinov, Neil L. Kelleher, Chad R. Weisbrod, Lissa C. Anderson, Julia Chamot-Rooke, Yunqiu Chen, John R. Yates, Luca Fornelli, Konstantin O. Nagornov, Lloyd M. Smith, Sneha Chatterjee, Ying Ge, Sung Hwan Yoon, Jolene K. Diedrich, Norelle C. Wildburger |
| المساهمون: | Centre de Recherche Pierre Fabre (Centre de R&D Pierre Fabre), PIERRE FABRE, Institut Pasteur [Paris], Institut Pasteur [Paris] (IP) |
| المصدر: | Journal of The American Society for Mass Spectrometry Journal of The American Society for Mass Spectrometry, Springer Verlag (Germany), 2020, 31 (9), pp.1783-1802. ⟨10.1021/jasms.0c00036⟩ Journal of the American Society for Mass Spectrometry Journal of the American Society for Mass Spectrometry, vol 31, iss 9 Journal of The American Society for Mass Spectrometry, 31(9), 1783-1802. AMER CHEMICAL SOC J Am Soc Mass Spectrom Journal of The American Society for Mass Spectrometry, 2020, 31 (9), pp.1783-1802. ⟨10.1021/jasms.0c00036⟩ |
| بيانات النشر: | AMER CHEMICAL SOC, 2020. |
| سنة النشر: | 2020 |
| مصطلحات موضوعية: | Proteomics, medicine.drug_class, [SDV]Life Sciences [q-bio], Computational biology, 010402 general chemistry, Tandem mass spectrometry, Monoclonal antibody, Mass spectrometry, 01 natural sciences, Article, Antibodies, Mass Spectrometry, FTMS, Analytical Chemistry, Mice, Medicinal and Biomolecular Chemistry, Structural Biology, Monoclonal, intact mass measurement, tandem mass spectrometry, medicine, MS/MS, Animals, Humans, Biology, Spectroscopy, [SDV.BBM.BS]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Structural Biology [q-bio.BM], Chemistry, 010401 analytical chemistry, Therapeutic protein, Antibodies, Monoclonal, Complementarity Determining Regions, 0104 chemical sciences, 3. Good health, Fourier transform mass spectrometry, Ion dissociation, glycoform, Therapeutic antibody, Biotechnology, Physical Chemistry (incl. Structural) |
| الوصف: | International audience; The Consortium for Top-Down Proteomics (www.topdownproteomics.org) launched the present study to assess the current state of top-down mass spectrometry (TD MS) and middle-down mass spectrometry (MD MS) for characterizing monoclonal antibody (mAb) primary structures, including their modifications. To meet the needs of the rapidly growing therapeutic antibody market, it is important to develop analytical strategies to characterize the heterogeneity of a therapeutic product's primary structure accurately and reproducibly. The major objective of the present study is to determine whether current TD/MD MS technologies and protocols can add value to the more commonly employed bottom-up (BU) approaches with regard to confirming protein integrity, sequencing variable domains, avoiding artifacts, and revealing modifications and their locations. We also aim to gather information on the common TD/MD MS methods and practices in the field. A panel of three mAbs was selected and centrally provided to 20 laboratories worldwide for the analysis: Sigma mAb standard (SiLuLite), NIST mAb standard, and the therapeutic mAb Herceptin (trastuzumab). Various MS instrument platforms and ion dissociation techniques were employed. The present study confirms that TD/MD MS tools are available in laboratories worldwide and provide complementary information to the BU approach that can be crucial for comprehensive mAb characterization. The current limitations, as well as possible solutions to overcome them, are also outlined. A primary limitation revealed by the results of the present study is that the expert knowledge in both experiment and data analysis is indispensable to practice TD/MD MS. |
| وصف الملف: | application/pdf |
| اللغة: | English |
| تدمد: | 1044-0305 1879-1123 |
| الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce93ac618ef03bef2381fe00d09bf9cfTest https://hdl.handle.net/1887/3182316Test |
| حقوق: | OPEN |
| رقم الانضمام: | edsair.doi.dedup.....ce93ac618ef03bef2381fe00d09bf9cf |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 10440305 18791123 |
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