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NIST Interlaboratory Study on Glycosylation Analysis of Monoclonal Antibodies
- Source :
- De Leoz, M L A, Duewer, D L, Fung, A, Liu, L, Yau, H K, Potter, O, Staples, G O, Furuki, K, Frenkel, R, Hu, Y, Sosic, Z, Zhang, P, Altmann, F, Gru Nwald-Grube, C, Shao, C, Zaia, J, Evers, W, Pengelley, S, Suckau, D, Wiechmann, A, Resemann, A, Jabs, W, Beck, A, Froehlich, J W, Huang, C, Li, Y, Liu, Y, Sun, S, Wang, Y, Seo, Y, An, H J, Reichardt, N C, Ruiz, J E, Archer-Hartmann, S, Azadi, P, Bell, L, Lakos, Z, An, Y, Cipollo, J F, Pucic-Bakovic, M, Štambuk, J, Lauc, G, Li, X, Wang, P G, Bock, A, Hennig, R, Rapp, E, Creskey, M, Cyr, T D, Nakano, M, Sugiyama, T, Leung, P K A, Link-Lenczowski, P, Jaworek, J, Yang, S, Zhang, H, Kelly, T, Klapoetke, S, Cao, R, Kim, J Y, Lee, H K, Lee, J Y, Yoo, J S, Kim, S R, Suh, S K, de Haan, N, Falck, D, Lageveen-Kammeijer, G S M, Wuhrer, M, Emery, R J, Kozak, R P, Liew, L P, Royle, L, Urbanowicz, P A, Packer, N H, Song, X, Everest-Dass, A, Lattová, E, Cajic, S, Alagesan, K, Kolarich, D, Kasali, T, Lindo, V, Chen, Y, Goswami, K, Gau, B, Amunugama, R, Jones, R, Stroop, C J M, Kato, K, Yagi, H, Kondo, S, Yuen, C T, Harazono, A, Shi, X, Magnelli, P E, Kasper, B T, Mahal, L, Harvey, D J, O'Flaherty, R, Rudd, P M, Saldova, R, Hecht, E S, Muddiman, D C, Kang, J, Bhoskar, P, Menard, D, Saati, A, Merle, C, Mast, S, Tep, S, Truong, J, Nishikaze, T, Sekiya, S, Shafer, A, Funaoka, S, Toyoda, M, de Vreugd, P, Caron, C, Pradhan, P, Tan, N C, Mechref, Y, Patil, S, Rohrer, J S, Chakrabarti, R, Dadke, D, Lahori, M, Zou, C, Cairo, C, Reiz, B, Whittal, R M, Lebrilla, C B, Wu, L, Guttman, A, Szigeti, M, Kremkow, B G, Lee, K H, Sihlbom, C, Adamczyk, B, Jin, C, Karlsson, N G, Örnros, J, Larson, G, Nilsson, J, Meyer, B, Wiegandt, A, Komatsu, E, Perreault, H, Bodnar, E D, Said, N, Francois, Y N, Leize-Wagner, E, Maier, S, Zeck, A, Heck, A J R, Yang, Y, Haselberg, R, Yu, Y Q, Alley, W, Leone, J W, Yuan, H & Stein, S E 2020, ' NIST Interlaboratory Study on Glycosylation Analysis of Monoclonal Antibodies : Comparison of Results from Diverse Analytical Methods ', MCP : Molecular & cellular proteomics, vol. 19, no. 1, pp. 11-30 . https://doi.org/10.1074/mcp.RA119.001677, Molecular and Cellular Proteomics, 19(1), 11-30. AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC, MCP : Molecular & cellular proteomics, 19(1), 11-30. American Society for Biochemistry and Molecular Biology Inc., Molecular & Cellular Proteomics, Molecular & Cellular Proteomics, 19(1), 11-30. AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC, Molecular and Cellular Proteomics, Molecular and Cellular Proteomics, American Society for Biochemistry and Molecular Biology, 2019, mcp.RA119.001677. ⟨10.1074/mcp.RA119.001677⟩, Molecular and Cellular Proteomics, 19(1), 11. American Society for Biochemistry and Molecular Biology Inc., Molecular & Cellular Proteomics : MCP
- Publication Year :
- 2020
- Publisher :
- American Society for Biochemistry and Molecular Biology Inc., 2020.
-
Abstract
- A broad-based interlaboratory study of glycosylation profiles of a reference and modified IgG antibody involving 103 reports from 76 laboratories.<br />Graphical Abstract Highlights A broad-based interlaboratory study of the glycosylation of a reference antibody: NISTmAb. 103 reports were received from 76 diverse laboratories worldwide. Analysis involved two samples, the NISTmAb and an enzymatically modified sample, enabling within-lab separation of random and systematic errors using the “Youden two-sample” method. Consensus values were derived and similar performance across all experimental methods was noted.<br />Glycosylation is a topic of intense current interest in the development of biopharmaceuticals because it is related to drug safety and efficacy. This work describes results of an interlaboratory study on the glycosylation of the Primary Sample (PS) of NISTmAb, a monoclonal antibody reference material. Seventy-six laboratories from industry, university, research, government, and hospital sectors in Europe, North America, Asia, and Australia submitted a total of 103 reports on glycan distributions. The principal objective of this study was to report and compare results for the full range of analytical methods presently used in the glycosylation analysis of mAbs. Therefore, participation was unrestricted, with laboratories choosing their own measurement techniques. Protein glycosylation was determined in various ways, including at the level of intact mAb, protein fragments, glycopeptides, or released glycans, using a wide variety of methods for derivatization, separation, identification, and quantification. Consequently, the diversity of results was enormous, with the number of glycan compositions identified by each laboratory ranging from 4 to 48. In total, one hundred sixteen glycan compositions were reported, of which 57 compositions could be assigned consensus abundance values. These consensus medians provide community-derived values for NISTmAb PS. Agreement with the consensus medians did not depend on the specific method or laboratory type. The study provides a view of the current state-of-the-art for biologic glycosylation measurement and suggests a clear need for harmonization of glycosylation analysis methods.
- Subjects :
- Proteomics
PROTEIN
fluerescence
Biochemistry
reference antibody
THERAPEUTIC ANTIBODIES
Biopharmaceutics
Analytical Chemistry
chemistry.chemical_compound
Biological sciences
Glycomics
NISTaAb
Analysis method
ComputingMilieux_MISCELLANEOUS
glycoproteins
mass spectrometry
chemistry.chemical_classification
0303 health sciences
glycan
interlaboratory study
030302 biochemistry & molecular biology
Glycopeptides
Antibodies, Monoclonal
3. Good health
glycomics
fluorescence
glycosylation
glycopeptide
NISTmAb
lipids (amino acids, peptides, and proteins)
Protein glycosylation
Glycan
Glycosylation
QUANTITATION
medicine.drug_class
Computational biology
Biology
Monoclonal antibody
03 medical and health sciences
GLYCOMIC ANALYSIS
SDG 3 - Good Health and Well-being
Polysaccharides
[CHIM.ANAL]Chemical Sciences/Analytical chemistry
Report
medicine
Humans
LC-MS/MS
Molecular Biology
030304 developmental biology
Biological Products
IDENTIFICATION
MASS-SPECTROMETRY
PROFILES
QUANTIFICATION
carbohydrates (lipids)
chemistry
biology.protein
Laboratories
Glycoprotein
Protein Processing, Post-Translational
Subjects
Details
- Language :
- English
- ISSN :
- 15359484 and 15359476
- Volume :
- 19
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- MCP : Molecular & cellular proteomics
- Accession number :
- edsair.doi.dedup.....4214e7f722323aeb909a6ec71f3d6bbd