Calculation of protein-ligand binding affinities

Annu Rev Biophys Biomol Struct. 2007;36:21-42. doi: 10.1146/annurev.biophys.36.040306.132550.

Abstract

Accurate methods of computing the affinity of a small molecule with a protein are needed to speed the discovery of new medications and biological probes. This paper reviews physics-based models of binding, beginning with a summary of the changes in potential energy, solvation energy, and configurational entropy that influence affinity, and a theoretical overview to frame the discussion of specific computational approaches. Important advances are reported in modeling protein-ligand energetics, such as the incorporation of electronic polarization and the use of quantum mechanical methods. Recent calculations suggest that changes in configurational entropy strongly oppose binding and must be included if accurate affinities are to be obtained. The linear interaction energy (LIE) and molecular mechanics Poisson-Boltzmann surface area (MM-PBSA) methods are analyzed, as are free energy pathway methods, which show promise and may be ready for more extensive testing. Ultimately, major improvements in modeling accuracy will likely require advances on multiple fronts, as well as continued validation against experiment.

Publication types

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

MeSH terms

  • Biophysics / methods
  • Drug Design
  • Electrolytes / chemistry
  • Entropy
  • Hydrogen-Ion Concentration
  • Ligands
  • Models, Theoretical
  • Molecular Conformation
  • Protein Binding*
  • Protein Conformation
  • Proteins / chemistry*
  • Quantum Theory
  • Software
  • Thermodynamics

Substances

  • Electrolytes
  • Ligands
  • Proteins