Yan Hao, Bhattarai Umesh, Guo Zhi-Fo, Liang Fu-Sen
Department of Chemistry and Chemical Biology, University of New Mexico , 300 Terrace Street NE, Albuquerque, New Mexico 87131, United States.
J Am Chem Soc. 2017 Apr 12;139(14):4987-4990. doi: 10.1021/jacs.7b00610. Epub 2017 Mar 29.
We report a new strategy to regulate microRNAs (miRNAs) biogenesis by using bifunctional small molecules that consist of a pre-miRNA binding unit connected by a linker to a Dicer inhibiting unit. In this effort, fluorescence polarization-based screening was used to identify neomycin as a pre-miR-21 binding ligand. Although neomycin cannot inhibit miR-21 maturation, linking it to the RNase inhibitor 1 forms the bifunctional conjugate 7A, which inhibits the production of miR-21. We expect that this strategy will be applicable to design other molecules for miRNA regulation.
我们报告了一种通过使用双功能小分子来调控微小RNA(miRNA)生物合成的新策略,该双功能小分子由通过接头连接到Dicer抑制单元的前体miRNA结合单元组成。在此过程中,基于荧光偏振的筛选被用于鉴定新霉素作为前体miR-21的结合配体。虽然新霉素不能抑制miR-21的成熟,但将其与核糖核酸酶抑制剂1连接形成双功能缀合物7A,可抑制miR-21的产生。我们期望这种策略将适用于设计其他用于调控miRNA的分子。