The inhibitory effects of toothpaste and mouthwash ingredients on the interaction between the SARS-CoV-2 spike protein and ACE2, and the protease activity of TMPRSS2 in vitro

被引:16
作者
Tateyama-Makino, Riho [1 ]
Abe-Yutori, Mari [1 ]
Iwamoto, Taku [1 ]
Tsutsumi, Kota [1 ]
Tsuji, Motonori [2 ]
Morishita, Satoru [1 ]
Kurita, Kei [1 ]
Yamamoto, Yukio [1 ]
Nishinaga, Eiji [1 ]
Tsukinoki, Keiichi [3 ]
机构
[1] Lion Corp, Res & Dev Headquarters, Edogawa Ku, Tokyo, Japan
[2] Inst Mol Funct, Misato, Saitama, Japan
[3] Kanagawa Dent Univ, Dept Oral Sci, Div Environm Pathol, Yokosuka, Kanagawa, Japan
来源
PLOS ONE | 2021年 / 16卷 / 09期
关键词
DOCKING; ACID;
D O I
10.1371/journal.pone.0257705
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
SARS-CoV-2 enters host cells when the viral spike protein is cleaved by transmembrane protease serine 2 (TMPRSS2) after binding to the host angiotensin-converting enzyme 2 (ACE2). Since ACE2 and TMPRSS2 are expressed in the tongue and gingival mucosa, the oral cavity is a potential entry point for SARS-CoV-2. This study evaluated the inhibitory effects of general ingredients of toothpastes and mouthwashes on the spike protein-ACE2 interaction and the TMPRSS2 protease activity using an in vitro assay. Both assays detected inhibitory effects of sodium tetradecene sulfonate, sodium N-lauroyl-N-methyltaurate, sodium N-lauroylsarcosinate, sodium dodecyl sulfate, and copper gluconate. Molecular docking simulations suggested that these ingredients could bind to inhibitor-binding site of ACE2. Furthermore, tranexamic acid exerted inhibitory effects on TMPRSS2 protease activity. Our findings suggest that these toothpaste and mouthwash ingredients could help prevent SARS-CoV-2 infection.
引用
收藏
页数:17
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