Rapid behavior-based identification of neuroactive small molecules in the zebrafish

被引:386
作者
Kokel, David [1 ,2 ,3 ]
Bryan, Jennifer [4 ,5 ]
Laggner, Christian [6 ]
White, Rick [4 ]
Cheung, Chung Yan J. [1 ,2 ,3 ]
Mateus, Rita [1 ,2 ,3 ]
Healey, David [1 ,2 ,3 ]
Kim, Sonia [1 ,2 ,3 ]
Werdich, Andreas A. [1 ,2 ]
Haggarty, Stephen J. [3 ,7 ,8 ]
MacRae, Calum A. [1 ,2 ]
Shoichet, Brian [6 ]
Peterson, Randall T. [1 ,2 ,3 ]
机构
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Cardiovasc Res Ctr, Charlestown, MA USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Div Cardiol,Dept Med, Charlestown, MA USA
[3] Broad Inst, Cambridge, MA USA
[4] Univ British Columbia, Dept Stat, Vancouver, BC V6T 1W5, Canada
[5] Univ British Columbia, Michael Smith Labs, Vancouver, BC V5Z 1M9, Canada
[6] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
[7] Massachusetts Gen Hosp, Ctr Human Genet Res, Boston, MA 02114 USA
[8] Stanley Ctr Psychiat Res, Cambridge, MA USA
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
ZINC-FINGER NUCLEASES; MONOAMINE OXIDASES; CHEMICAL GENETICS; DISCOVERY;
D O I
10.1038/NCHEMBIO.307
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
Neuroactive small molecules are indispensable tools for treating mental illnesses and dissecting nervous system function. However, it has been difficult to discover novel neuroactive drugs. Here, we describe a high-throughput, behavior-based approach to neuroactive small molecule discovery in the zebrafish. We used automated screening assays to evaluate thousands of chemical compounds and found that diverse classes of neuroactive molecules caused distinct patterns of behavior. These 'behavioral barcodes' can be used to rapidly identify new psychotropic chemicals and to predict their molecular targets. For example, we identified new acetylcholinesterase and monoamine oxidase inhibitors using phenotypic comparisons and computational techniques. By combining high-throughput screening technologies with behavioral phenotyping in vivo, behavior-based chemical screens can accelerate the pace of neuroactive drug discovery and provide small-molecule tools for understanding vertebrate behavior.
引用
收藏
页码:231 / 237
页数:7
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