4.7 Article

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

Journal

JOURNAL OF NATURAL PRODUCTS
Volume 70, Issue 3, Pages 383-390

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/np060555t

Keywords

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Funding

  1. NCI NIH HHS [R01 CA104569, R01 CA047135-17, CA 104569-01, CA 47135, R01 CA047135, R01 CA047135-19] Funding Source: Medline
  2. NCRR NIH HHS [S10 RR019918-018558, S10 RR019918, S10 RR022455, S10 RR 19918] Funding Source: Medline
  3. NIGMS NIH HHS [R29 GM056062, GM 56062-06, R01 GM056062] Funding Source: Medline

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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.

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