Affinity selection mass spectrometry speeding drug discovery

被引:10
|
作者
Prudent, Renaud [1 ]
Lemoine, Hugues [1 ]
Walsh, Jarrod [2 ]
Roche, Didier [1 ]
机构
[1] Edelris, Bioparc,Bioserra 1 Bldg, Lyon, France
[2] AstraZeneca, R&D BioPharmaceut, Discovery Sci, High Throughput Screening,Hit Discovery, Alderley Pk, England
关键词
af finity selection mass spectrometry; hit identi fication; drug discovery; COMBINATORIAL LIBRARIES; HIT IDENTIFICATION; LIGANDS; CHROMATOGRAPHY; TECHNOLOGIES; INHIBITORS; EVOLUTION; MAGMASS; SITE; MS;
D O I
10.1016/j.drudis.2023.103760
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Affinity selection mass spectrometry (AS-MS) has gained momentum in drug discovery. This review summarizes how this technology has slowly risen as a new paradigm in hit identification and its potential synergy with DNA encoded library technology. It presents an overview of the recent results on challenging targets and perspectives on new areas of research, such as RNA targeting with small molecules. The versatility of the approach is illustrated and strategic drivers discussed in terms of the experience of a small-medium CRO and a big pharma organization.
引用
收藏
页数:8
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