IUBMB Life · 1996 · 17 citations · 0 references
EngineeringBiochemistryLentil LectinDifferential Scanning CalorimetryBioanalysisIntrinsic FluorescenceBiochemical EngineeringPh 7.4Thermal ProcessingThermodynamicsCalorimetric MethodChromatographyMedicineChemical KineticsBiophysicsBiomolecular EngineeringKinetic StudyThermoanalytical Method
The irreversible thermal denaturation of lentil lectin was investigated at pH 7.4 using different techniques including high-sensitivity differential scanning calorimetry, differential detergent solubility thermal gel analysis, intrinsic fluorescence and hemagglutinating activity assays. The shape of the transition, as well as its scan-rate dependence, can be explained by assuming that thermal denaturation takes place according to the kinetic scheme N k-->D, where k is a first-order kinetic constant that changes with temperature, as given by the Arrhenius equation, N the native state, and D the denatured one. On the basis of this model, the value of the rate constant as a function of temperature and the activation energy were calculated. The analytical data obtained with the other methods used in this work support the proposed two-state kinetic model.