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    Structure, gating, and pharmacology of human CaV3.3 channel, Nat Commun, 19 Apr 2022

    發布時間:2022年04月19日

    Nature Communications, 19 April, 2022, DOI:https://doi.org/10.1038/s41467-022-29728-0

    Structure, gating, and pharmacology of human CaV3.3 channel

    Lingli He, Zhuoya Yu, Ze Geng, Zhuo Huang, Changjiang Zhang, Yanli Dong, Yiwei Gao, Yuhang Wang, Qihao Chen, Le Sun, Xinyue Ma, Bo Huang, Xiaoqun Wang & Yan Zhao

    Abstract

    The low-voltage activated T-type calcium channels regulate cellular excitability and oscillatory behavior of resting membrane potential which trigger many physiological events and have been implicated with many diseases. Here, we determine structures of the human T-type CaV3.3 channel, in the absence and presence of antihypertensive drug mibefradil, antispasmodic drug otilonium bromide and antipsychotic drug pimozide. CaV3.3 contains a long bended S6 helix from domain III, with a positive charged region protruding into the cytosol, which is critical for T-type CaV channel activation at low voltage. The drug-bound structures clearly illustrate how these structurally different compounds bind to the same central cavity inside the CaV3.3 channel, but are mediated by significantly distinct interactions between drugs and their surrounding residues. Phospholipid molecules penetrate into the central cavity in various extent to shape the binding pocket and play important roles in stabilizing the inhibitor. These structures elucidate mechanisms of channel gating, drug recognition, and actions, thus pointing the way to developing potent and subtype-specific drug for therapeutic treatments of related disorders.

    文章鏈接:https://www.nature.com/articles/s41467-022-29728-0

    相關報道:http://www.taobao183.com/kyjz/zxdt/202204/t20220422_6435791.html

     

     

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