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Free energy calculations for the relative binding affinity between DNA and lambda-repressor.

Minoru Saito·Akinori Sarai
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Abstract

The change in the binding free energy between DNA and lambda-repressor resulting from a base substitution, thymine (T)-->deoxyuracil (abbreviated as U), was evaluated by the free energy perturbation method on the basis of molecular dynamics simulations for the DNA-lambda-repressor complex in water with all degrees of freedom and including long-range Coulomb interactions. The binding free energy change that we calculated (1.47 +/- 0.40 kcal/mol) was in good agreement with an experimental value (1.8 kcal/mol). We clarified why the small difference between T and U (CH(3) in T is replaced with H in U) caused such a significant change in the binding free energy: The substitution of CH(3) in T with H in U lowered the dissociated-state free energy level due to the gain of the hydration free energy. Furthermore, the T-->U substitution raised the free energy level in the associated state due to the loss of the favored van der Waals (vdW) interactions with the lambda-repressor amino acid residues. In other words, the amino acid residues of lambda-repressor can recognize the CH(3) in T through the vdW interactions with the CH(3). This recognition is enhanced in a water environment, because the hydrophobic CH(3) prefers the amino acid residues of lambda-repressor to water molecules.

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Binding SitesComputer SimulationDNADNA-Binding ProteinsMathematical ComputingProtein BindingRepressor ProteinsThymineUracilViral ProteinsViral Regulatory and Accessory ProteinsWaterJournal Article

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Minoru Saito, Akinori Sarai. 2003-08-01. Free energy calculations for the relative binding affinity between DNA and lambda-repressor.. https://doi.org/10.1002/prot.10333

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