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NIST Interlaboratory Study on Glycosylation Analysis of Monoclonal Antibodies

Authors :
Miyako Nakano
Alena Wiegandt
Yunli Hu
Viv Lindo
Paulina A. Urbanowicz
Zsuzsanna Lakos
Cassie Caron
Song Klapoetke
Niels Christian Reichardt
Niclas Chiang Tan
Sandra Maier
Rene Hennig
Marton Szigeti
Ju Yeon Lee
Ying Qing Yu
Gregory O. Staples
Sachin Patil
Jolanta Jaworek
Waltraud Evers
Benjamin G. Kremkow
Youngsuk Seo
Kathirvel Alagesan
Yuetian Chen
Gordan Lauc
David L. Duewer
Yang Yang
Daniele Menard
Hyun Joo An
Tim Kelly
Stephen E. Stein
Joseph W. Leone
Anja Wiechmann
Ravi Amunugama
Peng George Wang
Clemens Grunwald-Grube
Maria Lorna A. De Leoz
Göran Larson
Rob Haselberg
Samanta Cajic
Stephanie A. Archer-Hartmann
Maja Pučić-Baković
Edward D. Bodnar
Pauline M. Rudd
Anja Resemann
Daniel Kolarich
Akira Harazono
Jeffrey S. Rohrer
Juan Echevarria Ruiz
Stuart Pengelley
Jong Shin Yoo
Arun V. Everest-Dass
Nicolle H. Packer
Steven W. Mast
William R. Alley
Erika Lattová
Anne Zeck
Corné J.M. Stroop
Radoslaw P. Kozak
Chun Shao
Alain Beck
Joseph Zaia
Erdmann Rapp
Lily Liu
Jennie Truong
Yaojun Wang
Christopher W. Cairo
Roisin O'Flaherty
Radka Saldova
Kudrat Goswami
Emy Komatsu
Jessica Örnros
Taiki Sugiyama
Prachi Bhoskar
Pralima Pradhan
Carlito B. Lebrilla
András Guttman
Christine Merle
Brian Kasper
Oscar G. Potter
Soo Kyung Suh
Li Phing Liew
Ranjan Chakrabarti
Terry D. Cyr
Sohei Funaoka
Masaaki Toyoda
Pui King Amy Leung
Toyin Kasali
Jerko Štambuk
Yanming An
Wolfgang Jabs
Bernd Meyer
Chunxia Zou
John F. Cipollo
Sa Rang Kim
Aaron Shafer
Randy M. Whittal
Jichao Kang
Albert J. R. Heck
Yehia Mechref
Hoi Kei Yau
Guinevere S. M. Lageveen-Kammeijer
Shiwei Sun
Kenichiro Furuki
Richard B. Jones
Béla Reiz
Niclas G. Karlsson
Mohammedazam Lahori
Xu Li
Barbara Adamczyk
Rui Cao
Lauren Wu
Koichi Kato
Detlev Suckau
Paweł Link-Lenczowski
Kelvin H. Lee
Xiaomin Song
Noortje de Haan
Ruth Frenkel
Adam Fung
Friedrich Altmann
Manfred Wuhrer
David Falck
Andreas Bock
Paula Magnelli
Brian Gau
Sachiko Kondo
Robert J. Emery
Chunsheng Jin
Louise Royle
David C. Muddiman
Hélène Perreault
John W. Froehlich
Disha Dadke
Peiqing Zhang
Lara K. Mahal
Takashi Nishikaze
Andrew Saati
Chuncui Huang
Hui Zhang
Carina Sihlbom
Parastoo Azadi
Jonas Nilsson
Yaming Liu
Yannis-Nicolas François
Nassur Said
Jin Young Kim
C. T. Yuen
Shuang Yang
Emmanuelle Leize-Wagner
David Harvey
Xiaofeng Shi
Yan Li
Hirokazu Yagi
Zoran Sosic
Elizabeth M. Hecht
Hua Yuan
Marybeth Creskey
Hyun Kyoung Lee
Sadanori Sekiya
Peter de Vreugd
Len Bell
Sam Tep
BioAnalytical Chemistry
AIMMS
Department of Plant and Microbial Biology
University of California
Laboratory of Infrared Material and Devices
Ningbo University (NBU)
University of Natural Resources and Life Sciences (BOKU)
Bruker Daltonik GmbH
Bruker Daltonik
Centre d'Immunologie Pierre Fabre
Xinjiang Agriculture University
Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN)
Instituto de Salud Carlos III [Madrid] (ISC)-ministerio de ciencia e innovacion
Complex Carbohydrate Research Center
University of Georgia [USA]
GENOS
Universität Duisburg-Essen [Essen]
Max Planck Institute for Dynamics of Complex Technical Systems
Max-Planck-Gesellschaft
Section de mathématiques [Genève]
Université de Genève (UNIGE)
Department of Computer Science [York] (CS-YORK)
University of York [York, UK]
State Key Laboratory of Hybrid Rice, Department of Genetics, College of Life Sciences
Wuhan University
LeidenUniversity Medical Center
University College Dublin [Dublin] (UCD)
Texas A&M University System
College of Engineering and Computer Science
Australian National University (ANU)
Unité de Recherche sur les Maladies Cardiovasculaires, du Métabolisme et de la Nutrition = Institute of cardiometabolism and nutrition (ICAN)
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière [AP-HP]
Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)
University of Edinburgh
University of Alberta
Department of Biological Sciences
Mass Spectrometry Facility
University of Alberta-Department of Chemistry
Volvo Car Corporation
Centre for Research in Intelligent Systems
Monash University [Clayton]
Department of Chemistry [Winnipeg, MB, Canada]
University of Manitoba [Winnipeg]
Department of Chemistry [Winnipeg, Manitoba, Canada]
Université de Strasbourg (UNISTRA)
Laboratoire de synthèses métallo-induites
Dynamique et structure moléculaire par spectrométrie de masse (LDSM2)
School of Mechanics and Engineering [Chengdu]
Southwest Jiaotong University (SWJTU)
School of Management and Economics [University of Electronic Science and Technology of China]
University of Electronic Science and Technology of China (UESTC)
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.

Details

Language :
English
ISSN :
15359484 and 15359476
Volume :
19
Issue :
1
Database :
OpenAIRE
Journal :
MCP : Molecular & cellular proteomics
Accession number :
edsair.doi.dedup.....4214e7f722323aeb909a6ec71f3d6bbd