Fragment-based screening by protein crystallography: successes and pitfalls

Int J Mol Sci. 2012 Oct 8;13(10):12857-79. doi: 10.3390/ijms131012857.

Abstract

Fragment-based drug discovery (FBDD) concerns the screening of low-molecular weight compounds against macromolecular targets of clinical relevance. These compounds act as starting points for the development of drugs. FBDD has evolved and grown in popularity over the past 15 years. In this paper, the rationale and technology behind the use of X-ray crystallography in fragment based screening (FBS) will be described, including fragment library design and use of synchrotron radiation and robotics for high-throughput X-ray data collection. Some recent uses of crystallography in FBS will be described in detail, including interrogation of the drug targets β-secretase, phenylethanolamine N-methyltransferase, phosphodiesterase 4A and Hsp90. These examples provide illustrations of projects where crystallography is straightforward or difficult, and where other screening methods can help overcome the limitations of crystallography necessitated by diffraction quality.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Amyloid Precursor Protein Secretases / chemistry
  • Binding Sites
  • Crystallography, X-Ray
  • Cyclic Nucleotide Phosphodiesterases, Type 4 / chemistry
  • Drug Design
  • HSP90 Heat-Shock Proteins / chemistry
  • Pharmaceutical Preparations / chemistry
  • Pharmaceutical Preparations / metabolism
  • Phenylethanolamine N-Methyltransferase / chemistry
  • Protein Structure, Tertiary
  • Proteins / chemistry*
  • Proteins / metabolism

Substances

  • HSP90 Heat-Shock Proteins
  • Pharmaceutical Preparations
  • Proteins
  • Phenylethanolamine N-Methyltransferase
  • Cyclic Nucleotide Phosphodiesterases, Type 4
  • Amyloid Precursor Protein Secretases