Screening strategies for identifying RNA- and ribonucleoprotein-targeted compounds

Trends Pharmacol Sci. 2021 Sep;42(9):758-771. doi: 10.1016/j.tips.2021.06.001. Epub 2021 Jun 29.

Abstract

The past few years have witnessed important breakthroughs in the identification of compounds that specifically bind and regulate RNAs and in optimizing them for therapeutic use. Here, we review successful and unsuccessful approaches in screening for RNA-targeted small molecules. We discuss advantages and disadvantages of the different screening techniques and variables that affect the outcome of RNA-screening projects. We also highlight key challenges that hamper the development of quality RNA ligands, especially the still-low availability of RNA-specific compound libraries and the poor understanding of RNA structural dynamics. We conclude that the development of new RNA-targeting drugs would greatly benefit from integration of the power of high-throughput screening technologies with improved biochemical, structural, and computational characterization of RNA targets.

Keywords: RNA computational biology; RNA ligand; RNA screening; affinity screen; gene reporter assay; mass spectrometry.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Drug Evaluation, Preclinical*
  • High-Throughput Screening Assays
  • Humans
  • Ligands
  • RNA*
  • Ribonucleoproteins*
  • Small Molecule Libraries

Substances

  • Ligands
  • Ribonucleoproteins
  • Small Molecule Libraries
  • RNA