The Discovery of Tyrosinase Enzyme Inhibitors Activity from Polyphenolic Compounds in Red Grape Seeds through In Silico Study

Mentari Luthfika Dewi, T. M. Fakih, Resty Imfyani Sofyan
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引用次数: 3

Abstract

Tyrosinases are essential metal-containing enzymes in the biosynthesis of melanin, therefore responsible for pigmentation of the skin. The upregulation of tyrosinase enzyme activities leads to hyperpigmentation that will become a health problems and interfere psychosocially. Inhibition of tyrosinase enzyme activity, both competitive and non-competitive become widely developed for most anti hyperpigmentation agent. Natural antioxidants are one of the potential compounds for this purpose. Red grape seeds contain high levels of antioxidant compounds, such as procyanidin, prodelphinidin, and propelargonidin. In this research in silico studies, including molecular docking, molecular dynamics simulations, and toxicity predictions, were used to assess the activity of the three molecules of polyphenolic compounds on macromolecules of the tyrosinase enzyme. Molecular docking studies show that the compound propelargonidin has the highest affinity against the macromolecule of the tyrosinase enzyme, with a binding free energy value of −32.87 kJ/mol. These results were confirmed in molecular dynamics simulations that show strong interactions at the macromolecular active site of the tyrosinase enzyme. Toxicity prediction results show that the three polyphenolic compound molecules were classified in the High-Class Category, which shows that safety is not guaranteed, but is likely, not carcinogenic and nongenotoxic. Therefore, the compound propelargonidin is predicted to be able to interact strongly with the tyrosinase enzyme. The results in this research are useful for further study in the development of tyrosinase enzyme inhibitors.
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红葡萄种子多酚类化合物酪氨酸酶抑制剂活性的硅晶研究
酪氨酸酶是黑色素生物合成中必需的含金属酶,因此负责皮肤的色素沉着。酪氨酸酶活性的上调导致色素沉着,这将成为一个健康问题,并干扰心理社会。抑制酪氨酸酶活性的竞争性和非竞争性已成为大多数抗色素沉着剂广泛发展的方向。天然抗氧化剂是实现这一目的的潜在化合物之一。红葡萄籽含有高水平的抗氧化化合物,如原花青素、原鸽苷和原花青素。在本研究中,采用分子对接、分子动力学模拟和毒性预测等方法,评估了三种多酚类化合物对酪氨酸酶大分子的活性。分子对接研究表明,化合物propelargonidin对酪氨酸酶的大分子具有最高的亲和力,结合自由能值为−32.87 kJ/mol。这些结果在分子动力学模拟中得到证实,表明酪氨酸酶的大分子活性位点有很强的相互作用。毒性预测结果表明,3种多酚类化合物分子属于高等级,安全性不保证,但有可能,不致癌,无遗传毒性。因此,化合物propelargonidin被预测能够与酪氨酸酶强烈相互作用。本研究结果对酪氨酸酶抑制剂的进一步开发具有一定的指导意义。
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