Discovery of Small Molecule WWP2 Ubiquitin Ligase Inhibitors

Chemistry. 2018 Dec 3;24(67):17677-17680. doi: 10.1002/chem.201804169. Epub 2018 Nov 6.

Abstract

We have screened small molecule libraries specifically for inhibitors that target WWP2, an E3 ubiquitin ligase associated with tumour outgrowth and spread. Selected hits demonstrated dose-dependent WWP2 inhibition, low micromolar IC50 values, and inhibition of PTEN substrate-specific ubiquitination. Binding to WWP2 was confirmed by ligand-based NMR spectroscopy. Furthermore, we used a combination of STD NMR, the recently developed DEEP-STD NMR approach, and docking calculations, to propose for the first time an NMR-validated 3D molecular model of a WWP2-inhibitor complex. These first generation WWP2 inhibitors provide a molecular framework for informing organic synthetic approaches to improve activity and selectivity.

Keywords: DEEP-STD NMR; drug discovery; inhibitors; saturation transfer difference NMR; ubiquitin ligase.

MeSH terms

  • Binding Sites
  • Drug Discovery
  • Enzyme Inhibitors / chemistry*
  • Enzyme Inhibitors / metabolism
  • Humans
  • Inhibitory Concentration 50
  • Ligands
  • Molecular Docking Simulation
  • Nuclear Magnetic Resonance, Biomolecular
  • PTEN Phosphohydrolase / metabolism
  • Protein Structure, Tertiary
  • Small Molecule Libraries / chemistry*
  • Small Molecule Libraries / metabolism
  • Solubility
  • Ubiquitin-Protein Ligases / antagonists & inhibitors*
  • Ubiquitin-Protein Ligases / metabolism

Substances

  • Enzyme Inhibitors
  • Ligands
  • Small Molecule Libraries
  • WWP2 protein, human
  • Ubiquitin-Protein Ligases
  • PTEN Phosphohydrolase