| Autor: |
Hering A; Department of Biology and Pharmaceutical Botany, Medical University of Gdansk, 80-210 Gdansk, Poland., Stefanowicz-Hajduk J; Department of Biology and Pharmaceutical Botany, Medical University of Gdansk, 80-210 Gdansk, Poland., Dziomba S; Department of Toxicology, Medical University of Gdansk, 80-210 Gdansk, Poland., Halasa R; Department of Pharmaceutical Microbiology, Medical University of Gdansk, 80-210 Gdansk, Poland., Krzemieniecki R; Department of Pharmaceutical Technology and Biochemistry, Faculty of Chemistry, Gdansk University of Technology, 80-233 Gdansk, Poland., Sappati S; Department of Pharmaceutical Technology and Biochemistry, Faculty of Chemistry, Gdansk University of Technology, 80-233 Gdansk, Poland., Baginski M; Department of Pharmaceutical Technology and Biochemistry, Faculty of Chemistry, Gdansk University of Technology, 80-233 Gdansk, Poland., Ochocka JR; Department of Biology and Pharmaceutical Botany, Medical University of Gdansk, 80-210 Gdansk, Poland. |
| Abstrakt: |
Mangiferin is a strong antioxidant that presents a wide range of biological activities. The aim of this study was to evaluate, for the first time, the influence of mangiferin on tyrosinase, an enzyme responsible for melanin synthesis and the unwanted browning process of food. The research included both the kinetics and molecular interactions between tyrosinase and mangiferin. The research proved that mangiferin inhibits tyrosinase activity in a dose-dependent manner with IC 50 290 +/- 6.04 µM, which was found comparable with the standard kojic acid (IC 50 217.45 +/- 2.54 µM). The mechanism of inhibition was described as mixed inhibition. The interaction between tyrosinase enzyme and mangiferin was confirmed with capillary electrophoresis (CE). The analysis indicated the formation of two main, and four less significant complexes. These results have also been supported by the molecular docking studies. It was indicated that mangiferin binds to tyrosinase, similarly to L-DOPA molecule, both in the active center and peripheral site. As it was presented in molecular docking studies, mangiferin and L-DOPA molecules can interact in a similar way with surrounding amino acid residues of tyrosinase. Additionally, hydroxyl groups of mangiferin may interact with amino acids on the tyrosinase external surface causing non-specific interaction. |
