Free energy of ligand binding to protein

Evaluation of the contribution of water molecules by computational methods

Pietro Cozzini, Micaela Fornabaio, Anna Marabotti, Donald J. Abraham, Glen E. Kellogs, Andrea Mozzarelli

Research output: Contribution to journalArticle

79 Citations (Scopus)

Abstract

One of the more challenging issues in medicinal chemistry is the computation of the free energy of ligand binding to macromolecular targets. This allows for the screening of libraries of chemicals for fast and inexpensive identification of lead compounds. Many attempts have been made and several algorithms have been developed for this purpose. Whereas enthalpic contributions are evaluated using methods and equations for which there is a reasonable consensus among researchers, the entropic contribution is evaluated using very different, and, in some cases, very approximate methods, or it is entirely ignored. Entropic contributions are of primary importance in the formation of many ligand-protein complexes, as well as in protein folding. The hydrophobic interaction, associated with the release of water molecules from the protein active site and the ligand, plays a significant role in complex formation, predominantly contributing to the total entropy change and, in some cases, to the total free energy of binding. There are distinct approaches for the evaluation of the contribution of water molecules to the free energy of binding based on Newtonian mechanics force fields, multi-parameter empirical scoring functions and experimental force fields. This review describes these methods - discussing both their advantages and limitations. Particular emphasis will be placed on HINT (Hydropatic INTeractions), a "natural" force field that takes into account in a unified way enthalpic and entropic contributions of all interacting atoms in protein-ligand complexes, including released and structured water molecules. As a case-study, the contribution of water molecules to the binding free energy of HIV-1 protease inhibitors is evaluated.

Original languageEnglish
Pages (from-to)3093-3118
Number of pages26
JournalCurrent Medicinal Chemistry
Volume11
Issue number23
Publication statusPublished - Dec 2004

Fingerprint

Computational methods
Free energy
Carrier Proteins
Ligands
Molecules
Water
Proteins
Small Molecule Libraries
HIV Protease Inhibitors
Lead compounds
Protein folding
Pharmaceutical Chemistry
Protein Folding
Entropy
Protease Inhibitors
Mechanics
Hydrophobic and Hydrophilic Interactions
Catalytic Domain
Screening
Research Personnel

Keywords

  • Binding free energy
  • Computational chemistry
  • Drug discovery
  • In silico screening
  • LogP
  • Protein crystallography
  • Scoring function
  • Water molecules

ASJC Scopus subject areas

  • Organic Chemistry
  • Biochemistry, Genetics and Molecular Biology(all)
  • Biochemistry
  • Pharmacology

Cite this

Cozzini, P., Fornabaio, M., Marabotti, A., Abraham, D. J., Kellogs, G. E., & Mozzarelli, A. (2004). Free energy of ligand binding to protein: Evaluation of the contribution of water molecules by computational methods. Current Medicinal Chemistry, 11(23), 3093-3118.

Free energy of ligand binding to protein : Evaluation of the contribution of water molecules by computational methods. / Cozzini, Pietro; Fornabaio, Micaela; Marabotti, Anna; Abraham, Donald J.; Kellogs, Glen E.; Mozzarelli, Andrea.

In: Current Medicinal Chemistry, Vol. 11, No. 23, 12.2004, p. 3093-3118.

Research output: Contribution to journalArticle

Cozzini, P, Fornabaio, M, Marabotti, A, Abraham, DJ, Kellogs, GE & Mozzarelli, A 2004, 'Free energy of ligand binding to protein: Evaluation of the contribution of water molecules by computational methods', Current Medicinal Chemistry, vol. 11, no. 23, pp. 3093-3118.
Cozzini P, Fornabaio M, Marabotti A, Abraham DJ, Kellogs GE, Mozzarelli A. Free energy of ligand binding to protein: Evaluation of the contribution of water molecules by computational methods. Current Medicinal Chemistry. 2004 Dec;11(23):3093-3118.
Cozzini, Pietro ; Fornabaio, Micaela ; Marabotti, Anna ; Abraham, Donald J. ; Kellogs, Glen E. ; Mozzarelli, Andrea. / Free energy of ligand binding to protein : Evaluation of the contribution of water molecules by computational methods. In: Current Medicinal Chemistry. 2004 ; Vol. 11, No. 23. pp. 3093-3118.
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