Discovery of Key Physicochemical, Structural, and Spatial Properties of RNA-Targeted Bioactive Ligands

被引:77
|
作者
Morgan, Brittany S. [1 ]
Forte, Jordan E. [1 ]
Culver, Rebecca N. [1 ]
Zhang, Yuqi [2 ]
Hargrove, Amanda E. [1 ]
机构
[1] Duke Univ, Dept Chem, Durham, NC 27708 USA
[2] Scripps Res Inst, Dept Integrat Struct & Computat Biol, La Jolla, CA 92037 USA
关键词
chemical probes; cheminformatics; molecular recognition; principal moments of inertia; RNA recognition; LONG NONCODING RNAS; SMALL MOLECULES; DRUG DISCOVERY; DESIGN; RECOGNITION; SEQUENCE; LIBRARY; SHAPE; DIVERSITY; DISEASE;
D O I
10.1002/anie.201707641
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
While a myriad non-coding RNAs are known to be essential in cellular processes and misregulated in diseases, the development of RNA-targeted small molecule probes has met with limited success. To elucidate the guiding principles for selective small molecule/RNA recognition, we analyzed cheminformatic and shape-based descriptors for 104 RNA-targeted ligands with demonstrated biological activity (RNA-targeted BIoactive ligaNd Database, R-BIND). We then compared R-BIND to both FDA-approved small molecule drugs and RNA ligands without reported bioactivity. Several striking trends emerged for bioactive RNA ligands, including: 1) Compliance to medicinal chemistry rules, 2) distinctive structural features, and 3) enrichment in rod-like shapes over others. This work provides unique insights that directly facilitate the selection and synthesis of RNA-targeted libraries with the goal of efficiently identifying selective small molecule ligands for therapeutically relevant RNAs.
引用
收藏
页码:13498 / 13502
页数:5
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