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康伊可托毒素对单 AMPA 型谷氨酸受体的作用。

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

机构信息

Leibniz Forschungsinstitut für Molekulare Pharmakologie, Berlin, Germany.

NeuroCure, Charité Universitätsmedizin, Berlin, Germany.

出版信息

J Gen Physiol. 2022 May 2;154(5). doi: 10.1085/jgp.202112912. Epub 2022 Apr 4.

Abstract

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.

摘要

短尾蚴毒素是一类由捕食性海蜗牛属 Conus 产生的天然存在的毒性肽,它们中的许多毒素针对离子通道,通常具有高度特异性和亲和力。因此,它们已被证明对基础研究非常有价值,并可作为治疗策略的先导。到目前为止,Con-ikot-ikot 是唯一一种被鉴定为针对 AMPA 型谷氨酸受体的短尾蚴毒素,AMPA 型谷氨酸受体是脊椎动物大脑中兴奋性神经递质的主要介质。在这里,我们描述了毒素如何在单通道水平上改变 AMPA 受体的活性。毒素与 AMPA 受体的结合 EC50 为 5 nM,一旦结合,需要数分钟才能洗出。如前所述,它能有效地阻断 AMPA 受体的脱敏;然而,与其他脱敏阻断剂相比,它不是开放通道的良好稳定剂,因为毒素结合的 AMPA 受体经常发生短暂的关闭。我们提出,这是毒素与配体结合域(LBD)独特结合模式的直接结果。与其他脱敏阻断剂不同,后者稳定 AMPA 受体四聚体中的单个二聚体,毒素固定四聚体的所有四个 LBD。这一结果进一步强调了独立 LBD 二聚体的四级重组对于 AMPA 受体的完全活性是必不可少的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c20/9195068/84cf307a5166/JGP_202112912_Fig1.jpg

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