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基于动物毒素研究预测钠通道孔的结构细节

Predicting Structural Details of the Sodium Channel Pore Basing on Animal Toxin Studies.

作者信息

Tikhonov Denis B, Zhorov Boris S

机构信息

Sechenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, Saint Petersburg, Russia.

Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON, Canada.

出版信息

Front Pharmacol. 2018 Aug 7;9:880. doi: 10.3389/fphar.2018.00880. eCollection 2018.

Abstract

Eukaryotic voltage-gated sodium channels play key roles in physiology and are targets for many toxins and medically important drugs. Physiology, pharmacology, and general architecture of the channels has long been the subject of intensive research in academia and industry. In particular, animal toxins such as tetrodotoxin, saxitoxin, and conotoxins have been used as molecular probes of the channel structure. More recently, X-ray structures of potassium and prokaryotic sodium channels allowed elaborating models of the toxin-channel complexes that integrated data from biophysical, electrophysiological, and mutational studies. Atomic level cryo-EM structures of eukaryotic sodium channels, which became available in 2017, show that the selectivity filter structure and other important features of the pore domain have been correctly predicted. This validates further employments of toxins and other small molecules as sensitive probes of fine structural details of ion channels.

摘要

真核生物电压门控钠通道在生理学中发挥着关键作用,并且是许多毒素和具有重要医学意义的药物的作用靶点。通道的生理学、药理学及总体结构长期以来一直是学术界和工业界深入研究的主题。特别是,河豚毒素、石房蛤毒素和芋螺毒素等动物毒素已被用作通道结构的分子探针。最近,钾通道和原核生物钠通道的X射线结构使得构建毒素-通道复合物模型成为可能,该模型整合了来自生物物理、电生理和突变研究的数据。2017年获得的真核生物钠通道的原子水平冷冻电镜结构表明,孔道结构域的选择性过滤器结构和其他重要特征已被正确预测。这进一步验证了将毒素和其他小分子用作离子通道精细结构细节的灵敏探针的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dee/6090064/982a52ad2c39/fphar-09-00880-g001.jpg

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