Surface plasmon resonance, molecular docking, and molecular dynamics simulation studies of lysozyme interaction with tannic acid

Lysozyme (LZM) is an important enzyme in medicine and industry. Tannic acid (TA) is used in brewing, wine industry, and as a food flavor enhancer. In nutritional and food science, LZM interacts with TA, notably in wine and saliva. This study aimed to investigate the binding interaction between LZM and TA using surface plasmon resonance, molecular docking, and molecular dynamics simulation. Chicken egg white lysozyme (CEWLZM) was applied as a model protein. Tri-N-acetylchitotriose (NAG3), the known inhibitor of CEWLZM, was used in the redocking experiments to determine the precise binding location within the complex. The average binding energies obtained from docking NAG3 and tannic acid to the target structure of CEWLZM were found to be -6.46 +/- 0.05 kcal/mol and -7.52 +/- 0.39 kcal/mol, respectively. The binding free energy of the CEWLZM-TA complex was then calculated as -27.61 kcal/mol by MMPBSA based on MD simulation trajectories. The observed interactions between the ligands and the lysozyme structure were mainly driven by hydrophobic, van der Waals, and H-bond interactions formed by the active site residues. MD simulations showed consistent and satisfactory binding distances between CEWLZM and TA throughout the analysis. SPR analysis was performed using 1X PBS buffer (pH 7.4) as coupling and running buffers, 30 mu L/min as flow rate, and 2.5 mg/mL CEWLZM. Serial concentrations of TA (20-150 mu M) were injected through immobilized CEWLZM, and the KD value of CEWLZM-TA binding was obtained as 4.17 x 10-5 M. This study could enhance existing literature and pave the way for future research in food science and oral biology.

The interaction between chicken egg white lysozyme (CEWLZM) and tannic acid (TA) was investigated using computational techniques and SPR binding analysis. The computational results showed average binding energies and minimum distance values for the CEWLZM-TA interaction and the number of H-bond formations in this complex. For the experimental study, SPR analysis was used to determine the KD value of CEWLZM-TA binding. This study could enhance existing literature and pave the way for future research in food science and oral biology.image