Small molecule inhibition of RISC loading

ACS Chem Biol. 2012 Feb 17;7(2):403-10. doi: 10.1021/cb200253h. Epub 2011 Nov 11.

Abstract

Argonaute proteins are the core components of the microRNP/RISC. The biogenesis and function of microRNAs and endo- and exo- siRNAs are regulated by Ago2, an Argonaute protein with RNA binding and nuclease activities. Currently, there are no in vitro assays suitable for large-scale screening of microRNP/RISC loading modulators. We describe a novel in vitro assay that is based on fluorescence polarization of TAMRA-labeled RNAs loaded to human Ago2. Using this assay, we identified potent small-molecule inhibitors of RISC loading, including aurintricarboxylic acid (IC(50) = 0.47 μM), suramin (IC(50) = 0.69 μM), and oxidopamine HCL (IC(50) = 1.61 μM). Small molecules identified by this biochemical screening assay also inhibited siRNA loading to endogenous Ago2 in cultured cells.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Argonaute Proteins / metabolism*
  • Cell Line
  • DNA / metabolism
  • Drug Evaluation, Preclinical / methods*
  • Fluorescent Dyes / analysis
  • Humans
  • RNA / analysis*
  • RNA / metabolism
  • RNA, Small Interfering / antagonists & inhibitors
  • RNA, Small Interfering / metabolism
  • RNA-Induced Silencing Complex / antagonists & inhibitors*
  • RNA-Induced Silencing Complex / metabolism
  • Rhodamines / analysis
  • Small Molecule Libraries / chemistry*
  • Small Molecule Libraries / pharmacology*

Substances

  • 5-carboxytetramethylrhodamine succinimidyl ester
  • AGO2 protein, human
  • Argonaute Proteins
  • Fluorescent Dyes
  • RNA, Small Interfering
  • RNA-Induced Silencing Complex
  • Rhodamines
  • Small Molecule Libraries
  • RNA
  • DNA