HDX-MS guided drug discovery: small molecules and biopharmaceuticals

被引:73
|
作者
Marciano, David P. [1 ]
Dharmarajan, Venkatasubramanian [1 ]
Griffin, Patrick R. [1 ]
机构
[1] Scripps Res Inst, Mol Therapeut Dept, Jupiter, FL 33458 USA
关键词
EXCHANGE MASS-SPECTROMETRY; HYDROGEN-DEUTERIUM EXCHANGE; PROTEIN-LIGAND INTERACTIONS; ELECTRON-TRANSFER DISSOCIATION; BETA(2) ADRENERGIC-RECEPTOR; HYDROGEN/DEUTERIUM-EXCHANGE; PPAR-GAMMA; H/D EXCHANGE; COUPLED RECEPTORS; CONFORMATIONAL DYNAMICS;
D O I
10.1016/j.sbi.2014.08.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hydrogen/deuterium exchange coupled with mass spectrometry (HDX-MS or DXMS) has emerged as an important tool for the development of small molecule therapeutics and biopharmaceuticals. Central to these advances have been improvements to automated HDX-MS platforms and software that allow for the rapid acquisition and processing of experimental data. Correlating the HDX-MS profile of large numbers of ligands with their functional outputs has enabled the development of structure activity relationships (SAR) and delineation of ligand classes based on functional selectivity. HDX-MS has also been applied to address many of the unique challenges posed by the continued emergence of biopharmaceuticals. Here we review the latest applications of HDX-MS to drug discovery, recent advances in technology and software, and provide perspective on future outlook.
引用
收藏
页码:105 / 111
页数:7
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