Identifying Interactions that Determine Fragment Binding at Protein Hotspots

J Med Chem. 2016 May 12;59(9):4314-25. doi: 10.1021/acs.jmedchem.5b01980. Epub 2016 Apr 11.

Abstract

Locating a ligand-binding site is an important first step in structure-guided drug discovery, but current methods do little to suggest which interactions within a pocket are the most important for binding. Here we illustrate a method that samples atomic hotspots with simple molecular probes to produce fragment hotspot maps. These maps specifically highlight fragment-binding sites and their corresponding pharmacophores. For ligand-bound structures, they provide an intuitive visual guide within the binding site, directing medicinal chemists where to grow the molecule and alerting them to suboptimal interactions within the original hit. The fragment hotspot map calculation is validated using experimental binding positions of 21 fragments and subsequent lead molecules. The ligands are found in high scoring areas of the fragment hotspot maps, with fragment atoms having a median percentage rank of 97%. Protein kinase B and pantothenate synthetase are examined in detail. In each case, the fragment hotspot maps are able to rationalize a Free-Wilson analysis of SAR data from a fragment-based drug design project.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Ligands
  • Molecular Dynamics Simulation
  • Peptide Synthases / chemistry
  • Protein Binding
  • Proteins / chemistry*
  • Proto-Oncogene Proteins c-akt / chemistry

Substances

  • Ligands
  • Proteins
  • Proto-Oncogene Proteins c-akt
  • Peptide Synthases
  • pantothenate synthetase