دورية أكاديمية
Polynuclear Ruthenium Amines Inhibit K2P Channels via a 'Finger in the Dam' Mechanism
| العنوان: | Polynuclear Ruthenium Amines Inhibit K2P Channels via a 'Finger in the Dam' Mechanism |
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| المؤلفون: | Pope, Lianne, Lolicato, Marco, Minor, Daniel L |
| المساهمون: | Pope, Lianne, Lolicato, Marco, Minor, Daniel L |
| سنة النشر: | 2020 |
| المجموعة: | IRIS UNIPV (Università degli studi di Pavia) |
| مصطلحات موضوعية: | CAP domain, K2P channel, Keystone inhibitor site, Ru360, X-ray crystallography, electrophysiology, ruthenium red |
| الوصف: | The trinuclear ruthenium amine ruthenium red (RuR) inhibits diverse ion channels, including K2P potassium channels, TRPs, the calcium uniporter, CALHMs, ryanodine receptors, and Piezos. Despite this extraordinary array, there is limited information for how RuR engages targets. Here, using X-ray crystallographic and electrophysiological studies of an RuR-sensitive K2P, K2P2.1 (TREK-1) I110D, we show that RuR acts by binding an acidic residue pair comprising the "Keystone inhibitor site" under the K2P CAP domain archway above the channel pore. We further establish that Ru360, a dinuclear ruthenium amine not known to affect K2Ps, inhibits RuR-sensitive K2Ps using the same mechanism. Structural knowledge enabled a generalizable design strategy for creating K2P RuR "super-responders" having nanomolar sensitivity. Together, the data define a "finger in the dam" inhibition mechanism acting at a novel K2P inhibitor binding site. These findings highlight the polysite nature of K2P pharmacology and provide a new framework for K2P inhibitor development. |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| العلاقة: | info:eu-repo/semantics/altIdentifier/pmid/32059793; journal:CELL CHEMICAL BIOLOGY; http://hdl.handle.net/11571/1318906Test |
| DOI: | 10.1016/j.chembiol.2020.01.011 |
| الإتاحة: | https://doi.org/10.1016/j.chembiol.2020.01.011Test http://hdl.handle.net/11571/1318906Test |
| رقم الانضمام: | edsbas.2121A762 |
| قاعدة البيانات: | BASE |
| DOI: | 10.1016/j.chembiol.2020.01.011 |
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