Identification of a small-molecule ligand of the epigenetic reader protein Spindlin1 via a versatile screening platform

Nucleic Acids Res. 2016 May 19;44(9):e88. doi: 10.1093/nar/gkw089. Epub 2016 Feb 17.

Abstract

Epigenetic modifications of histone tails play an essential role in the regulation of eukaryotic transcription. Writer and eraser enzymes establish and maintain the epigenetic code by creating or removing posttranslational marks. Specific binding proteins, called readers, recognize the modifications and mediate epigenetic signalling. Here, we present a versatile assay platform for the investigation of the interaction between methyl lysine readers and their ligands. This can be utilized for the screening of small-molecule inhibitors of such protein-protein interactions and the detailed characterization of the inhibition. Our platform is constructed in a modular way consisting of orthogonal in vitro binding assays for ligand screening and verification of initial hits and biophysical, label-free techniques for further kinetic characterization of confirmed ligands. A stability assay for the investigation of target engagement in a cellular context complements the platform. We applied the complete evaluation chain to the Tudor domain containing protein Spindlin1 and established the in vitro test systems for the double Tudor domain of the histone demethylase JMJD2C. We finally conducted an exploratory screen for inhibitors of the interaction between Spindlin1 and H3K4me3 and identified A366 as the first nanomolar small-molecule ligand of a Tudor domain containing methyl lysine reader.

MeSH terms

  • Cell Cycle Proteins / metabolism*
  • Cell Line, Tumor
  • Epigenesis, Genetic / genetics*
  • HL-60 Cells
  • Histone Methyltransferases
  • Histone-Lysine N-Methyltransferase / metabolism
  • Histones / metabolism*
  • Humans
  • Jumonji Domain-Containing Histone Demethylases / metabolism
  • Ligands
  • Lysine / chemistry
  • Methylation
  • Microtubule-Associated Proteins / metabolism*
  • Phosphoproteins / metabolism*
  • Protein Binding / physiology
  • Protein Domains
  • Protein Processing, Post-Translational / physiology*

Substances

  • Cell Cycle Proteins
  • Histones
  • KDM4C protein, human
  • Ligands
  • Microtubule-Associated Proteins
  • Phosphoproteins
  • spindlin
  • Jumonji Domain-Containing Histone Demethylases
  • Histone Methyltransferases
  • Histone-Lysine N-Methyltransferase
  • Lysine