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Investigation of the Linear Response Approximation for Predicting Hydration Free Energies
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Teknisk-naturvetenskapliga fakulteten, Biologiska sektionen, Institutionen för cell- och molekylärbiologi.
Manuskript (Annet vitenskapelig)
Identifikatorer
URN: urn:nbn:se:uu:diva-95288OAI: oai:DiVA.org:uu-95288DiVA, id: diva2:169448
Tilgjengelig fra: 2006-12-22 Laget: 2006-12-22 Sist oppdatert: 2010-01-13bibliografisk kontrollert
Inngår i avhandling
1. Computational Methods for Calculation of Ligand-Receptor Binding Affinities Involving Protein and Nucleic Acid Complexes
Åpne denne publikasjonen i ny fane eller vindu >>Computational Methods for Calculation of Ligand-Receptor Binding Affinities Involving Protein and Nucleic Acid Complexes
2007 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

The ability to accurately predict binding free energies from computer simulations is an invaluable resource in understanding biochemical processes and drug action. Several methods based on microscopic molecular dynamics simulations exist, and in this thesis the validation, application, and development of the linear interaction energy (LIE) method is presented.

For a test case of several hydrophobic ligands binding to P450cam it is found that the LIE parameters do not change when simulations are performed with three different force fields. The nonpolar contribution to binding of these ligands is best reproduced with a constant offset and a previously determined scaling of the van der Waals interactions.

A new methodology for prediction of binding free energies of protein-protein complexes is investigated and found to give excellent agreement with experimental results. In order to reproduce the nonpolar contribution to binding, a different scaling of the van der Waals interactions is neccesary (compared to small ligand binding) and found to be, in part, due to an electrostatic preorganization effect not present when binding small ligands.

A new treatment of the electrostatic contribution to binding is also proposed. In this new scheme, the chemical makeup of the ligand determines the scaling of the electrostatic ligand interaction energies. These scaling factors are calibrated using the electrostatic contribution to hydration free energies and proposed to be applicable to ligand binding.

The issue of codon-anticodon recognition on the ribosome is adressed using LIE. The calculated binding free energies are in excellent agreement with experimental results, and further predict that the Leu2 anticodon stem loop is about 10 times more stable than the Ser stem loop in complex with a ribosome loaded with the Phe UUU codon. The simulations also support the previously suggested roles of A1492, A1493, and G530 in the codon-anticodon recognition process.

sted, utgiver, år, opplag, sider
Uppsala: Acta Universitatis Upsaliensis, 2007. s. 53
Serie
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1651-6214 ; 255
Emneord
Theoretical chemistry, computer simulations, molecular dynamics, linear interaction energy, binding free energy, linear response, protein-protein interactions, structure-based design, point mutations, hot spots, solvation free energy, Teoretisk kemi
Identifikatorer
urn:nbn:se:uu:diva-7421 (URN)91-554-6761-X (ISBN)
Disputas
2007-01-19, B7:101, BMC, Husargatan 3, Uppsala, 13:15
Opponent
Veileder
Tilgjengelig fra: 2006-12-22 Laget: 2006-12-22bibliografisk kontrollert

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