Research on the Interaction Mechanism and Structural Changes in Human Serum Albumin with Hispidin Using Spectroscopy and Molecular Docking
Open Access
Abstract
The interaction between human serum albumin (HSA) and hispidin, a polyketide abundantly present in both edible and therapeutic mushrooms, was explored through multispectral methods, hydrophobic probe assays, location competition trials, and molecular docking simulations. The results of fluorescence quenching analysis showed that hispidin quenched the fluorescence of HSA by binding to it via a static mechanism. The binding of hispidin and HSA was validated further by synchronous fluorescence, three-dimensional fluorescence, and UV/vis spectroscopy analysis. The apparent binding constant (Ka) at different temperatures, the binding site number (n), the quenching constants (Ksv), the dimolecular quenching rate constants (Kq), and the thermodynamic parameters (∆G, ∆H, and ∆S) were calculated. Among these parameters, ∆H and ∆S were determined to be 98.75 kJ/mol and 426.29 J/(mol·K), respectively, both exhibiting positive values. This observation suggested a predominant contribution of hydrophobic forces in the interaction between hispidin and HSA. By employing detergents (SDS and urea) and hydrophobic probes (ANS), it became feasible to quantify alterations in Ka and surface hydrophobicity, respectively. These measurements confirmed the pivotal role of hydrophobic forces in steering the interaction between hispidin and HSA. Site competition experiments showed that there was an interaction between hispidin and HSA molecules at site I, which situates the IIA domains of HSA, which was further confirmed by the molecular docking simulation.Keywords
Funding Information
- Natural Science Foundation of Guangdong Province (2021A1515010615, 2022A1515012520, 2021S0052, 2023S003040, 2023S002024, 2022DZXHT015, 2022S035, 2022S036)
- Special Fund for Science and Technology Innovation Strategy of Guangdong Province (2021A1515010615, 2022A1515012520, 2021S0052, 2023S003040, 2023S002024, 2022DZXHT015, 2022S035, 2022S036)
- Special Fund for Science and Technology of Maoming City (2021A1515010615, 2022A1515012520, 2021S0052, 2023S003040, 2023S002024, 2022DZXHT015, 2022S035, 2022S036)
This publication has 62 references indexed in Scilit:
- Studies on the interaction of gallic acid with human serum albumin in membrane mimetic environmentsTalanta, 2008
- Flavonoid–serum albumin complexation: determination of binding constants and binding sites by fluorescence spectroscopyBiochimica et Biophysica Acta (BBA) - General Subjects, 2005
- Binding of genistein to human serum albumin demonstrated using tryptophan fluorescence quenchingInternational Journal of Biological Macromolecules, 2004
- Thermal stability of β-lactoglobulins A and B: effect of SDS, urea, cysteine and N-ethylmaleimideJournal of Dairy Research, 2004
- Probing the binding of the flavonoid, quercetin to human serum albumin by circular dichroism, electronic absorption spectroscopy and molecular modelling methodsBiochemical Pharmacology, 2003
- Crystal Structure Analysis of Warfarin Binding to Human Serum AlbuminJournal of Biological Chemistry, 2001
- Ligand-Binding Proteins: Their Potential for Application in Systems for Controlled Delivery and Uptake of LigandsPharmacological Reviews, 2000
- Synthetic hispidin, a PKC inhibitor, is more cytotoxic toward cancer cells than normal cells in vitroCell Biology and Toxicology, 1997
- The Characterization of Two Specific Drug Binding Sites on Human Serum AlbuminMolecular Pharmacology, 1975
- Cooperative Effects in Binding by Bovine Serum Albumin. II. The Binding of 1-Anilino-8-naphthalenesulfonate. Polarization of the Ligand Fluorescence and Quenching of the Protein Fluorescence*Biochemistry, 1966