How Chemoproteomics Can Enable Drug Discovery and Development

被引:126
作者
Moellering, Raymond E. [1 ,2 ]
Cravatt, Benjamin F. [1 ,2 ]
机构
[1] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Physiol Chem, La Jolla, CA 92037 USA
来源
CHEMISTRY & BIOLOGY | 2012年 / 19卷 / 01期
关键词
ACTIVITY-BASED PROBES; HISTONE DEACETYLASE COMPLEXES; MOLECULE KINASE INHIBITORS; SERINE HYDROLASES; PLASMODIUM-FALCIPARUM; SELECTIVE INHIBITOR; MALARIA PARASITE; PYRUVATE-KINASE; IN-VIVO; CANCER;
D O I
10.1016/j.chembiol.2012.01.001
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
Creating first-in-class medications to treat human disease is an extremely challenging endeavor. While genome sequencing and genetics are making direct connections between mutations and human disorders at an unprecedented rate, matching molecular targets with a suitable therapeutic indication must ultimately be achieved by pharmacology. Here, we discuss how the integration of chemical proteomic platforms (such as activity-based protein profiling) into the earliest stages of the drug discovery process has the potential to greatly expand the scope of proteins that can be pharmacologically evaluated in living systems, and, through doing so, promote the identification and prioritization of new therapeutic targets.
引用
收藏
页码:11 / 22
页数:12
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