Characterization of the interaction between tartrazine and β-lactoglobulin under different pH conditions: multispectral analysis and computer simulation
Abstract
Unraveling the interaction mechanism between the food azo dye tartrazine (Tz) and β-lactoglobulin (β-LG) under varying pH conditions is crucial for understanding their safe application in food systems. Molecular docking indicated that Tz primarily bound to the β-hydrophobic barrel of β-LG. The protonation of lysine residues diminished with increasing pH, which reduced hydrogen bond formation. The binding energy decreased from 8.77 kcal/mol (pH 2.0) to 8.43 kcal/mol (pH 7.4). Molecular dynamics simulations indicated that Tz bound exerts the greatest structural influence on β-LG at pH 2.0. Fluorescence and thermodynamic analyses confirmed that Tz quenched β-LG fluorescence through a static mechanism, through their interaction was a spontaneous process driven mainly by hydrophobic forces. The protonation level of β-LG gradually decreased with increasing pH, and electrostatic repulsion between β-LG and Tz was observed at pH 7.4. As a result, the binding constant between Tz and β-LG decreased from 6.669 × 105 L/mol (pH 2.0) to 3.596 × 105 L/mol (pH 5.2) and 0.956 × 105 L/mol (pH 7.4), respectively. Furthermore, Tz induced changes in the secondary structure content of β-LG and reduced its surface hydrophobicity under all pH conditions.
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