Department of Chemistry, The Scripps Research Institute, Jupiter, Florida 33458.
Cold Spring Harb Perspect Biol. 2018 Nov 1;10(11):a034769. doi: 10.1101/cshperspect.a034769.
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.
虽然我们生活在 RNA 世界的残余物中,但药物发现和化学探针的世界仍然以蛋白质为中心。开发针对 RNA 的高选择性小分子通常被认为是一个难以逾越的挑战。我们的目标是揭开这类化合物设计的神秘面纱。在这篇综述中,我们描述了从序列设计靶向 RNA 的小分子的各种方法,以及这些化合物在 RNA 生物学中的应用,重点是抑制人类 RNA-蛋白质复合物。我们开发了一种库对库筛选方法来定义选择性的 RNA-小分子结合伙伴,并将其应用于致病 RNA,特别是非编码致癌 RNA 和扩展的 RNA 重复序列,以调节它们在细胞和动物中的生物学功能。我们还描述了新型小分子探针的设计,这些探针可以广泛揭示细胞中 RNA 的奥秘。