Mills Nicholas L, Shelat Anang A, Guy R Kiplin
Graduate Program in Chemistry and Chemical Biology, University of California, San Francisco, USA.
J Biomol Screen. 2007 Oct;12(7):946-55. doi: 10.1177/1087057107306128.
The lack of lead compounds that specifically recognize and manipulate the function of RNA molecules limits our ability to consider RNA targets valid for drug discovery. Herein is reported a high-throughput biochemical screen for inhibitors of RNA-protein interactions based on AlphaScreen technology that incorporates several layers of specificity measurements into the primary screen. This screen was used to analyze approximately 5500 compounds from a collection of bioactive small molecules to detect inhibitors of the HIV-1 Rev-RRE and BIV Tat-TAR interactions. This proof-of-concept screen validates the assay as one that accurately identifies hit molecules and determines the selectivity of those hits.
缺乏能够特异性识别并调控RNA分子功能的先导化合物,限制了我们将RNA靶点视为有效药物发现靶点的能力。本文报道了一种基于AlphaScreen技术的用于RNA-蛋白质相互作用抑制剂的高通量生化筛选方法,该方法在初次筛选中纳入了多层特异性测量。此筛选用于分析来自生物活性小分子集合的约5500种化合物,以检测HIV-1 Rev-RRE和BIV Tat-TAR相互作用的抑制剂。这一概念验证筛选证实了该检测方法能够准确识别命中分子并确定这些命中分子的选择性。