Hydrogen deuterium exchange mass spectrometry in biopharmaceutical discovery and development - A review

被引:64
|
作者
Deng, Bin [1 ,2 ]
Lento, Cristina [1 ,2 ]
Wilson, Derek J. [1 ,2 ]
机构
[1] York Univ, Dept Chem, 4700 Keele St, Toronto, ON M3J 1P3, Canada
[2] York Univ, Ctr Res Mass Spectrometry, Toronto, ON M3J 1P3, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Hydrogen deuterium exchange; Mass spectrometry; Drug discovery and development; Protein therapeutics; Biosimilar; Biopharmaceutical industry; PROTEIN-LIGAND INTERACTIONS; IGG1; MONOCLONAL-ANTIBODY; REACTION CHAMBER VOLUME; HIGHER-ORDER STRUCTURE; X-RAY CRYSTALLOGRAPHY; ATP-BINDING-SITE; HYDROGEN/DEUTERIUM-EXCHANGE; CONFORMATIONAL DYNAMICS; H/D EXCHANGE; HDX-MS;
D O I
10.1016/j.aca.2016.08.006
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Protein therapeutics have emerged as a major class of biopharmaceuticals over the past several decades, a trend that has motivated the advancement of bioanalytical technologies for protein therapeutic characterization. Hydrogen deuterium exchange mass spectrometry (HDX-MS) is a powerful and sensitive technique that can probe the higher order structure of proteins and has been used in the assessment and development of monoclonal antibodies (mAbs), antibody-drug conjugates (ADCs) and biosimilar antibodies. It has also been used to quantify protein-ligand, protein-receptor and other protein-protein interactions involved in signaling pathways. In manufacturing and development, HDXMS can validate storage formulations and manufacturing processes for various biotherapeutics. Currently, HDX-MS is being refined to provide additional coverage, sensitivity and structural specificity and implemented on the millisecond timescale to reveal residual structure and dynamics in disordered domains and intrinsically disordered proteins. (C) 2016 Elsevier B. V. All rights reserved.
引用
收藏
页码:8 / 20
页数:13
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