Publication | Closed Access
First principles calculations of thermodynamics and kinetic parameters and molecular dynamics simulations of acetylcholinesterase reactivators: can mouse data provide new insights into humans?
19
Citations
72
References
2012
Year
Bioorganic ChemistryKinetic Reactivation ConstantsFirst Principles CalculationsEnzymatic ModificationRedox BiologyOxidative StressTheoretical MethodologyBioanalysisStructure-function Enzyme KineticsAcetylcholinesterase ReactivatorsBiophysicsAldehyde DehydrogenaseBiochemistryKinetic ParametersBiochemical InteractionBiomolecular InteractionPharmacologyCellular EnzymologyNatural SciencesEnzyme CatalysisMedicineComputational Biophysics
We have applied a theoretical methodology, previously developed to evaluate the association and kinetic reactivation constants of oximes, comparing theoretical data obtained for human acetylcholinesterase (HsAChE) with in vitro results from Mus musculus AChE (MmAChE) previously reported in the literature. Our results, further checked by additional molecular dynamics simulations steps, showed a good correlation between the theoretical and experimental data, supporting the methodology as appropriate for prediction of thermodynamic and kinetic parameters and corroborated MmAChE as a suitable model for studies with HsAChE.
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