Impact of linker strain and flexibility in the design of a fragment-based inhibitor

Nat Chem Biol. 2009 Jun;5(6):407-13. doi: 10.1038/nchembio.163. Epub 2009 Apr 26.

Abstract

The linking together of molecular fragments that bind to adjacent sites on an enzyme can lead to high-affinity inhibitors. Ideally, this strategy would use linkers that do not perturb the optimal binding geometries of the fragments and do not have excessive conformational flexibility that would increase the entropic penalty of binding. In reality, these aims are seldom realized owing to limitations in linker chemistry. Here we systematically explore the energetic and structural effects of rigid and flexible linkers on the binding of a fragment-based inhibitor of human uracil DNA glycosylase. Analysis of the free energies of binding in combination with cocrystal structures shows that the flexibility and strain of a given linker can have a substantial impact on binding affinity even when the binding fragments are optimally positioned. Such effects are not apparent from inspection of structures and underscore the importance of linker optimization in fragment-based drug discovery efforts.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Enzyme Inhibitors / chemistry*
  • Enzyme Inhibitors / pharmacology
  • Humans
  • Magnetic Resonance Spectroscopy
  • Mass Spectrometry
  • Models, Molecular
  • Uracil-DNA Glycosidase / antagonists & inhibitors*

Substances

  • Enzyme Inhibitors
  • Uracil-DNA Glycosidase

Associated data

  • PDB/2HXM
  • PDB/3FCF
  • PDB/3FCI
  • PDB/3FCK
  • PDB/3FCL
  • PubChem-Substance/57551971
  • PubChem-Substance/57551972
  • PubChem-Substance/57551973
  • PubChem-Substance/57551974
  • PubChem-Substance/57551975
  • PubChem-Substance/57551976
  • PubChem-Substance/57551977
  • PubChem-Substance/57551978
  • PubChem-Substance/57551979
  • PubChem-Substance/57551980
  • PubChem-Substance/57551981
  • PubChem-Substance/57551982
  • PubChem-Substance/57551983
  • PubChem-Substance/57551984
  • PubChem-Substance/57551985
  • PubChem-Substance/57551986
  • PubChem-Substance/57551987
  • PubChem-Substance/57551988
  • PubChem-Substance/57551989
  • PubChem-Substance/57551990
  • PubChem-Substance/57551991
  • PubChem-Substance/57551992
  • PubChem-Substance/57551993
  • PubChem-Substance/57551994
  • PubChem-Substance/57551995
  • PubChem-Substance/57551996
  • PubChem-Substance/57551997
  • PubChem-Substance/57551998
  • PubChem-Substance/57551999
  • PubChem-Substance/57552000
  • PubChem-Substance/57552001
  • PubChem-Substance/57552002
  • PubChem-Substance/57552003
  • PubChem-Substance/57552004
  • PubChem-Substance/57552005
  • PubChem-Substance/57552006