The action of Con-ikot-ikot toxin on single AMPA-type glutamate receptors

被引:3
|
作者
Baranovic, Jelena [1 ,2 ,3 ,4 ]
Braunbeck, Sebastian [1 ,2 ,3 ]
Zaki, Nikolai [1 ,2 ,3 ]
Minniberger, Sonja [1 ,2 ,3 ]
Chebli, Miriam [1 ,2 ]
Plested, Andrew J. R. [1 ,2 ,3 ]
机构
[1] Leibniz Forschungsinst Mol Pharmakol, Berlin, Germany
[2] Charite Univ Med Berlin, NeuroCure, Berlin, Germany
[3] Humboldt Univ, Inst Biol Cellular Biophys, Berlin, Germany
[4] Univ Edinburgh, Sch Biol Sci, Edinburgh, Midlothian, Scotland
来源
JOURNAL OF GENERAL PHYSIOLOGY | 2022年 / 154卷 / 05期
基金
欧洲研究理事会; 英国惠康基金;
关键词
LIGAND-BINDING DOMAIN; CROSS-LINKING; DESENSITIZATION; CYCLOTHIAZIDE; MODULATION; ACTIVATION; MECHANISM; PROTEINS; DYNAMICS; MUTATION;
D O I
10.1085/jgp.202112912
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Conotoxins are a large group of naturally occurring toxic peptides produced by the predatory sea snails of the genus Conus. Many of these toxins target ion channels, often with high specificity and affinity. As such, they have proven to be invaluable for basic research, as well as acting as leads for therapeutic strategies. Con-ikot-ikot is the only conotoxin so far identified that targets AMPA-type glutamate receptors, the main mediators of excitatory neurotransmission in the vertebrate brain. Here, we describe how the toxin modifies the activity of AMPA receptors at the single-channel level. The toxin binds to the AMPA receptor with EC50 of 5 nM, and once bound takes minutes to wash out. As shown previously, it effectively blocks desensitization of AMPA receptors; however, compared to other desensitization blockers, it is a poor stabilizer of the open channel because toxin-bound AMPA receptors undergo frequent brief closures. We propose that this is a direct consequence of the toxin's unique binding mode to the ligand-binding domains (LBDs). Unlike other blockers of desensitization, which stabilize individual dimers within an AMPA receptor tetramer, the toxin immobilizes all four LBDs of the tetramer. This result further emphasizes that quaternary reorganization of independent LBD dimers is essential for the full activity of AMPA receptors.
引用
收藏
页数:17
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