Rediscovering the sweet spot in drug discovery

被引:137
作者
Brown, D [1 ]
Superti-Furga, G [1 ]
机构
[1] Cellzome AG, Elstree WD6 3SH, Herts, England
关键词
PROTEIN-PROTEIN INTERACTIONS; SIGNAL-TRANSDUCTION; MASS-SPECTROMETRY; PROTEOMICS; TARGETS; COMPLEXES; IDENTIFICATION; PURIFICATION; ORGANIZATION; INHIBITORS;
D O I
10.1016/S1359-6446(03)02902-7
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Advances over the past decade in drug discovery technologies have not yet led to an increase in productivity. We analyzed the reasons that have led to this juncture and identify the selection of the right target and the right lead as crucial. New approaches are required to take full advantage of the genomics revolution. For targets, methods are becoming available for high-throughput proteome analysis and pathway characterization that synergize with studies of disease association and differential expression. For leads, methods are being developed that 'reverse' the high-throughput screening paradigm by mapping drugs and drug-like compounds back onto the proteome. The synergy between pathway mapping and compound mapping could allow the pharmaceutical and biotechnology industries to rediscover the sweet spot of research productivity.
引用
收藏
页码:1067 / 1077
页数:11
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