1 Program in Chemical Biology, University of Michigan, Ann Arbor, Michigan, USA.
3 Center for Chemical Genomics, Life Sciences Institute, University of Michigan, Ann Arbor, Michigan, USA.
SLAS Discov. 2018 Jan;23(1):47-54. doi: 10.1177/2472555217717944. Epub 2017 Jul 7.
microRNAs (miRNAs) are small gene regulatory RNAs, and their expression has been found to be dysregulated in a number of human diseases. To facilitate the discovery of small molecules capable of selectively modulating the activity of a specific miRNA, we have utilized new high-throughput screening technology targeting Dicer-mediated pre-miRNA maturation. Pilot screening of ~50,000 small molecules and ~33,000 natural product extract libraries against pre-miR-21 processing indicated the potential of our assay for this goal, yielding a campaign Z' factor of 0.52 and an average plate signal-to-background (S/B) ratio of 13. Using two-dimensional screening against a second pre-miRNA, pre-let-7d, we evaluated the selectivity of confirmed hits. The results presented demonstrate how high-throughput screening can be used to identify selective small molecules for a target RNA.
微小 RNA(miRNA)是小的基因调控 RNA,其表达在许多人类疾病中被发现失调。为了促进发现能够选择性调节特定 miRNA 活性的小分子,我们利用了针对 Dicer 介导的 pre-miRNA 成熟的新的高通量筛选技术。针对 pre-miR-21 加工对约 50,000 种小分子和约 33,000 种天然产物提取物文库的初步筛选表明,我们的测定法具有实现这一目标的潜力,其测定法 Z' 因子为 0.52,平均板信号背景比(S/B)为 13。通过针对第二个 pre-miRNA,pre-let-7d 的二维筛选,我们评估了确认的命中的选择性。呈现的结果表明了如何使用高通量筛选来鉴定针对靶 RNA 的选择性小分子。