Abstract
A novel tiered Structure-Based (SB) Virtual Screening (VS) workflow called tieredScreen was designed and implemented. The automated protocol utilises diverse computational tools in a synergistic manner to reduce false positives and increase the likelihood of converging on putative active molecules. The performance of the novel VS workflow was validated using the Directory of Useful Decoys (DUD) Estrogen Receptor α (ERα) antagonist dataset, and successfully deployed for the identification of novel antagonists of ERa from a screening collection of ca. 160000 commercially available compounds. As well as yielding nanomolar (nM) active ligands identified previously through a docking only protocol, from a selection of eight virtual hits suggested by tieredScreen, four novel nM ERa binding chemotypes were identified and biologically validated - demonstrating the applicability of a tiered intervention for virtual screening.
| Original language | English |
|---|---|
| Pages (from-to) | 421-430 |
| Number of pages | 10 |
| Journal | Molecular Informatics |
| Volume | 29 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - 17 May 2010 |
Keywords
- Docking
- Drug Design
- Estrogen receptor
- Molecular modelling
- Nuclear hormone receptor
- Pharmacophore
- Shape matching
- Virtual screening