Isolindleyin exerts anti-melanogenic effects in human epidermal melanocytes via direct binding to tyrosinase

被引:4
作者
Lee, Ji Young [1 ,2 ]
Kim, Juewon [1 ]
Nam, Yeon Joo [3 ]
Kim, Hyoung-june [1 ]
No, Kyoung Tai [2 ,4 ]
机构
[1] Amorepacific Corp R&D Ctr, Yongin 17074, Gyeonggi Do, South Korea
[2] Yonsei Univ, Biomat Sci & Engn, Seoul 03722, South Korea
[3] Gyeonggido Business & Sci Acceleator, Bioctr, Suwon 16229, South Korea
[4] Yonsei Univ, Bioinformat & Mol Design Res Ctr BMDRC, Incheon 21983, South Korea
关键词
Isolindleyin; Anti-melanogenic effects; Human epidermal melanocytes; Tyrosinase; SKIN;
D O I
10.1016/j.bbrc.2020.10.105
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To overcome dermatological concerns causing abnormally excessive melanin synthesis, highly effective and safe skin depigmentation compounds have been identified in the cosmetic and pharmaceutical industries. Among several methods used to achieve skin depigmentation, inhibition of tyrosinase is one of the most effective, since tyrosinase is a crucial enzyme in melanogenesis. Herein, isolindleyin, a novel inhibitor of human tyrosinase, was introduced and evaluated for its anti-melanogenic effects in human epidermal melanocytes. The results revealed that isolindleyin was directly bound to tyrosinase and it suppressed melanin synthesis. The binding mode between isolindleyin and the active sites of human tyrosinase was investigated using computational molecular docking at the atomic level. Isolindleyin binding was found to be stabilized by hydrophobic interactions between His 367 and Val 377 and by hydrogen bonds between Ser 380 and Asn 364. The results of this study revealed the anti-melanogenic effects of isolindleyin that could contribute toward overcoming dermatological concerns that cause abnormally excessive melanin synthesis. (C) 2020 Published by Elsevier Inc.
引用
收藏
页码:802 / 807
页数:6
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