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Accelerating the Discovery of Biologically Active Small Molecules Using a High-Throughput Yeast Halo Assay

N.C. Gassner, Craig M. Tamble, Jonathan Bock, Naomi Cotton, Kimberly N. White, Karen Tenney, Robert P. St.Onge, Michael Proctor, Guri Giaever, Corey Nislow, Ronald W. Davis, Phillip Crews, Theodore R. Holman, R. Scott Lokey

发表年份
2007
引用次数
57

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.

关键词

YeastHigh-throughput screeningSaccharomyces cerevisiaeAntifungalFractionationBiological activityBudding yeastDrug discoverySmall moleculePhenotypic screening

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