Drugging the RNA World

被引:42
作者
Disney, Matthew D. [1 ]
Dwyer, Brendan G. [1 ]
Childs-Disney, Jessica L. [1 ]
机构
[1] Scripps Res Inst, Dept Chem, Jupiter, FL 33458 USA
基金
美国国家卫生研究院;
关键词
MYOTONIC-DYSTROPHY TYPE-1; PRE-MESSENGER-RNA; GREEN FLUORESCENT PROTEIN; SMALL-MOLECULE INHIBITION; SEQUENCE-BASED DESIGN; 16S RIBOSOMAL-RNA; SECONDARY STRUCTURE; TELOMERASE RNA; TARGETING RNA; FRONTOTEMPORAL DEMENTIA;
D O I
10.1101/cshperspect.a034769
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Although we live in the remnants of an RNA world, the world of drug discovery and chemical probes is firmly protein-centric. Developing highly selective small molecules targeting RNA is often considered to be an insurmountable challenge. Our goal is to demystify the design of such compounds. In this review, we describe various approaches to design small molecules that target RNA from sequence and the application of these compounds in RNA biology, with a focus on inhibition of human RNA-protein complexes. We have developed a library-versus-library screening approach to define selective RNA-small-molecule binding partners and applied them to disease-causing RNAs, in particular noncoding oncogenic RNAs and expanded RNA repeats, to modulate their biology in cells and animals. We also describe the design of new types of small-molecule probes that could broadly decipher the mysteries of RNA in cells.
引用
收藏
页数:15
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