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Density functional theory calculations on entire proteins for free energies of binding: Application to a model polar binding site
Abstrakt
In drug optimization calculations, the molecular mechanics Poisson-Boltzmann surface area (MM-PBSA) method can be used to compute free energies of binding of ligands to proteins. The method involves the evaluation of the energy of configurations in an implicit solvent model. One source of errors is the force field used, which can potentially lead to large errors due to the restrictions in accuracy imposed by its empirical nature. To assess the effect of the force field on the calculation of binding energies, in this article we use large-scale density functional theory (DFT) calculations as an alternative method to evaluate the energies of the configurations in a “QM-PBSA” approach. Our DFT calculations are performed with a near-complete basis set and a minimal parameter implicit solvent model, within the self-consistent calculation, using the ONETEP program on protein–ligand complexes containing more than 2600 atoms. We apply this approach to the T4-lysozyme double mutant L99A/M102Q protein, which is a well-studied model of a polar binding site, using a set of eight small aromatic ligands. We observe that there is very good correlation between the MM and QM binding energies in vacuum but less so in the solvent. The relative binding free energies from DFT are more accurate than the ones from the MM calculations, and give markedly better agreement with experiment for six of the eight ligands. Furthermore, in contrast to MM-PBSA, QM-PBSA is able to correctly predict a nonbinder
Cytowania
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Autorzy (5)
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Stephen Fox
- University of Southampton School of Chemistry
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Thomas Fox
- Boehringer Ingelheim Pharma GmbH Brak - autor pracuje w przemyśle
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Christofer Tautermann
- Boehringer Ingelheim Pharma GmbH Brak - autor pracuje w przemyśle
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Chris-Kriton Skylaris
- University of Southampton School of Chemistry
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Pełna treść
- Wersja publikacji
- Accepted albo Published Version
- DOI:
- Cyfrowy identyfikator dokumentu elektronicznego (otwiera się w nowej karcie) 10.1002/prot.24686
- Licencja
- Copyright (2014 Wiley Periodicals, Inc.)
Słowa kluczowe
Informacje szczegółowe
- Kategoria:
- Publikacja w czasopiśmie
- Typ:
- artykuł w czasopiśmie wyróżnionym w JCR
- Opublikowano w:
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PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS
nr 82,
wydanie 12,
strony 3335 - 3346,
ISSN: 0887-3585 - Język:
- angielski
- Rok wydania:
- 2014
- Opis bibliograficzny:
- Fox S., Dziedzic J., Fox T., Tautermann C., Skylaris C.: Density functional theory calculations on entire proteins for free energies of binding: Application to a model polar binding site// PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS. -Vol. 82, iss. 12 (2014), s.3335-3346
- DOI:
- Cyfrowy identyfikator dokumentu elektronicznego (otwiera się w nowej karcie) 10.1002/prot.24686
- Weryfikacja:
- Politechnika Gdańska
wyświetlono 243 razy
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