Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.628657
Title: Development and application of free energy methods
Author: Schopf, Patrick
Awarding Body: University of Southampton
Current Institution: University of Southampton
Date of Award: 2013
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Abstract:
The development of free energy simulation protocols for calculating relative binding free energies of ligands is presented in this thesis. To this end, the protein Dihydroorotate Dehydrogenase (DHODH), complexed to a highly congeneric series of compounds that show ambiguities in their binding modes, was studied in detail. To estimate the systematic error in force fields, relative free energies of hydration have been calculated using Replica-exchange Thermodynamic Integration (RETI) for sets of force field parameters and atomic partial charges in a classical molecular mechanics environment as well as a novel hybrid molecular mechanics/quantum mechanics model. The results demonstrated that all force fields and methods employed yield similar estimates of the relative free energies, while GAFF and OPLS-AA in conjunction with AM1BCC and AM1CM1A charges, respectively, performed best. To balance accuracy and ease of generating parameters, GAFF in conjunction with AM1BCC charges was selected to be the most valuable for describing the inhibitors in DHODH. To rigorously assess the thermodynamic end states for the ligands, crystal hydrates present in the binding site of DHODH have been investigated using the Just-Add-Water-molecules (JAWS) algorithm, Grand-canonical Monte Carlo (GCMC) simulations and the double-decoupling approach (DDM). These findings clearly suggested a change in hydration networks for both the inhibitors and their different binding modes, while all three approaches essentially yield identical results. This allowed us to construct free energy cycles using the single and dual topology approach in order to calculate the free energies of binding of the ligands as well as the stability of their binding modes. The results obtained were precise within the error of the methods, but not accurate, and allowed to complement the crystallographic findings.
Supervisor: Essex, Jonathan Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.628657  DOI: Not available
Keywords: QD Chemistry
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