Accelerating the discovery of biologically active small molecules using a high-throughput yeast halo assay

被引:41
作者
Gassner, Nadine C.
Tamble, Craig M.
Bock, Jonathan E.
Cotton, Naomi
White, Kimberly N.
Tenney, Karen
St Onge, Robert P.
Proctor, Michael J.
Giaever, Guri
Nislow, Corey
Davis, Ronald W.
Crews, Phillip [1 ]
Holman, Theodore R.
Lokey, R. Scott
机构
[1] Univ Calif Santa Cruz, Dept Chem & Biochem, Santa Cruz, CA 95064 USA
[2] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
[3] Stanford Genome Technol Ctr, Palo Alto, CA 94304 USA
[4] Univ Toronto, Fac Pharm, Donnelly Ctr Cellular & Biomol Res, Toronto, ON M5S3E1, Canada
[5] Stanford Univ, Sch Med, Dept Biochem, Stanford, CA 94305 USA
来源
JOURNAL OF NATURAL PRODUCTS | 2007年 / 70卷 / 03期
关键词
D O I
10.1021/np060555t
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The budding yeast Saccharomyces cerevisiae, a powerful model system for the study of basic eukaryotic cell biology, has been used increasingly as a screening tool for the identification of bioactive small molecules. We have developed a novel yeast toxicity screen that is easily automated and compatible with high-throughput screening robotics. The new screen is quantitative and allows inhibitory potencies to be determined, since the diffusion of the sample provides a concentration gradient and a corresponding toxicity halo. The efficacy of this new screen was illustrated by testing materials including 3104 compounds from the NCI libraries, 167 marine sponge crude extracts, and 149 crude marine-derived fungal extracts. There were 46 active compounds among the NCI set. One very active extract was selected for bioactivity-guided fractionation, resulting in the identification of crambescidin 800 as a potent antifungal agent.
引用
收藏
页码:383 / 390
页数:8
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