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• W2998960137 abstract "<span style=color: #1f497d;>Introduction: Beta-Boswellic acid (BBA) is a pentacyclic terpene which has been obtained from frankincense and its beneficial effects on neurodegenerative disorders such as Alzheimer’s disease (AD) have been addressed.<br /> <span style=color: #1f497d;>Methods: In the present study, thermodynamic and kinetic aspects of BBA interaction with Tau protein as one of the important proteins involved in AD in the absence and presence of glucose has been investigated using surface plasmon resonance (SPR) method. Tau protein was immobilized onto the carboxy methyl dextran chip and its binding interactions with BBA were studied at physiological pH at various temperatures. Glucose interference with these interactions was also investigated.<br /> <span style=color: #1f497d;>Results: Results showed that BBA forms a stable complex with Tau (KD=8.45×10-7 M) at 298 K. Molecular modeling analysis showed a hydrophobic interaction between BBA and HVPGGG segment of R2 and R4 repeated domains of Tau.<br /> <span style=color: #1f497d;>Conclusion: The binding affinity increased by temperature enhancement, while it decreased significantly in the presence of glucose. Both association and dissociation of the BBA-Tau complex were accompanied with an entropic activation barrier; however, positive enthalpy and entropy changes revealed that hydrophobic bonding is the main force involved in the interaction." @default.
• W2998960137 created "2020-01-23" @default.
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• W2998960137 date "2019-05-22" @default.
• W2998960137 modified "2023-10-17" @default.
• W2998960137 title "Kinetic and thermodynamic study of beta-Boswellic acid interaction with Tau protein investigated by surface plasmon resonance and molecular modeling methods" @default.
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• W2998960137 doi "https://doi.org/10.15171/bi.2020.03" @default.
• W2998960137 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6977593" @default.
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