Activation of TMEM16A by natural product canthaxanthin promotes gastrointestinal contraction

被引:12
|
作者
Ji, Qiushuang [1 ,2 ]
Shi, Sai [1 ,3 ]
Guo, Shuai [1 ,3 ]
Zhan, Yong [1 ,3 ]
Zhang, Hailin [4 ]
Chen, Yafei [1 ]
An, Hailong [1 ,3 ]
机构
[1] Hebei Univ Technol, Sch Sci, Inst Biophys, Key Lab Mol Biophys, Tianjin, Hebei, Peoples R China
[2] Tianjin Univ, Sch Pharmaceut Sci & Technol, Tianjin, Peoples R China
[3] Hebei Univ Technol, Sch Elect Engn, Tianjin, Peoples R China
[4] Hebei Med Univ, Dept Pharmacol, Key Lab Neural & Vasc Biol, Key Lab Pharmacol & Toxicol New Drug,Minist Educ, Shijiazhuang, Hebei, Peoples R China
来源
FASEB JOURNAL | 2020年 / 34卷 / 10期
基金
中国国家自然科学基金;
关键词
activator; binding site; canthaxanthin; ileal contraction; TMEM16A; CHLORIDE CHANNEL; INTERSTITIAL-CELLS; TRANSMEMBRANE PROTEIN; SWISS-MODEL; CL-CHANNEL; CAJAL; CONTRIBUTES; INHIBITION; EXPRESSION; CFTR;
D O I
10.1096/fj.202000443RR
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
Transmembrane 16A (TMEM16A), also known as anoctamin 1, is the molecular basis of the calcium-activated chloride channels. TMEM16A is present in interstitial cells of Cajal, which are the pacemaker cells that control smooth muscle contraction. TMEM16A is implicated in gastrointestinal disorders. Activation of TMEM16A is believed to promote the gastrointestinal muscle contraction. Here, we report a highly efficient, nontoxic, and selective activator of TMEM16A, canthaxanthin (CX). The study using molecular docking and site-directed mutation revealed that CX-specific binging site in TMEM16A is K769. CX was also found to promote the contraction of smooth muscle cells in gastrointestinal tract through activation of TMEM16A channels, which provides an excellent basis for development of CX as a chemical tool and potential therapeutic for gastrointestinal dysfunction.
引用
收藏
页码:13430 / 13444
页数:15
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