Publication | Open Access
Avoiding accuracy-limiting pitfalls in the study of protein-ligand interactions with isothermal titration calorimetry
25
Citations
9
References
2015
Year
Unknown Venue
EngineeringDifferential Scanning CalorimetryComputational ChemistryMolecular ThermodynamicsProtein FoldingCalibrationBioanalysisAccuracy-limiting PitfallsTrack PrecisionProtocol DesignMolecular SimulationThermodynamicsComputational BiochemistryBiophysicsThermoanalytical MethodProtein ChemistryMolecular SciencesBiochemistryChemometricsChemometric MethodBiomedical AnalysisBiomolecular InteractionCalorimetric MethodComputational ModelingMolecular ModelingProtein-ligand InteractionsBiomolecular ScienceMedicineDrug DiscoveryIsothermal Titration Calorimetry
Abstract Isothermal titration calorimetry (ITC) can yield precise (3%) estimates of the thermodynamic parameters describing biomolecular association (affinity, enthalpy, and entropy), making it an indispensable tool for biochemistry and drug discovery. Surprisingly, interlaboratory comparisons suggest that errors of ∽ 20% are common and widely underreported. Here, we show how to reduce precision- and accuracy-limiting errors while obtaining good estimates and minimizing material and time consumed by an experiment. We provide a simple spreadsheet that allows practitioners to identify precision-limiting operations during protocol design, track precision during the experiment, and propagate error to yield realistic final uncertainties.
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