Accounting for water molecules in drug design

Sergio E. Wong, Felice C Lightstone

Research output: Contribution to journalArticlepeer-review

64 Scopus citations

Abstract

Importance of the field: Water molecules often appear around ligands in protein crystal structures. Reliable prediction of the effects of water on ligand binding remains a challenge. Solvation effects are crucial for lead optimization where a 100-fold difference in binding affinity is significant but correspond to only ∼3 kcal/mol in binding free energy. Well-known examples, such as nonpeptidic urea inhibitors of HIV protease, prove that careful examination of water molecules and their energetics can contribute significantly to a successful drug design campaign. Areas covered in this review: In this review, we examine methods to account for the effect of water in ligand binding at two stages of drug discovery: lead identification via docking calculations and lead optimization. We provide a survey of the models and techniques available to account for water in drug design. What the reader will gain: The reader will become aware of common practices and pitfalls in dealing with water molecules in structure-based drug design. Take home message: Although solvation effects are not fully understood, some pragmatic recommendations at the end of the article provide guidance for modelers in this area as well as new practitioners.

Original languageEnglish (US)
Pages (from-to)65-74
Number of pages10
JournalExpert Opinion on Drug Discovery
Volume6
Issue number1
DOIs
StatePublished - Jan 2011
Externally publishedYes

Keywords

  • Computation
  • Docking
  • Drug design
  • Hit identification
  • Lead identification
  • Lead optimization
  • Water

ASJC Scopus subject areas

  • Drug Discovery

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