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-Structure paper
タイトル | Structures of TASK-1 and TASK-3 K2P channels provide insight into their gating and dysfunction in disease. |
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ジャーナル・号・ページ | Structure, Vol. 33, Issue 1, Page 115-122.e4, Year 2025 |
掲載日 | 2025年1月2日 |
![]() | Peter Rory Hall / Thibault Jouen-Tachoire / Marcus Schewe / Peter Proks / Thomas Baukrowitz / Elisabeth P Carpenter / Simon Newstead / Karin E J Rödström / Stephen J Tucker / ![]() ![]() |
PubMed 要旨 | TASK-1 and TASK-3 are pH-sensitive two-pore domain (K2P/KCNK) K channels. Their functional roles make them promising targets for treatment of multiple disorders including sleep apnea, pain, and ...TASK-1 and TASK-3 are pH-sensitive two-pore domain (K2P/KCNK) K channels. Their functional roles make them promising targets for treatment of multiple disorders including sleep apnea, pain, and atrial fibrillation. Mutations in these channels are also associated with neurodevelopmental and hypertensive disorders. A previous crystal structure of TASK-1 revealed a lower "X-gate" as a hotspot for missense gain-of-function (GoF) mutations associated with DDSA (developmental delay with sleep apnea). However, the mechanisms of gating in TASK channels are still not fully understood. Here, we resolve structures for both human TASK-1 and TASK-3 by cryoelectron microscopy (cryo-EM), as well as a recurrent TASK-3 variant (G236R) associated with KCNK9 imprinting syndrome (KIS) (formerly known as Birk-Barel syndrome). Combined with functional studies of the X-gating mechanism, we provide evidence for how a highly conserved gating mechanism becomes defective in disease, and also provide further insight into the pathway of conformational changes that underlie the pH-dependent inhibition of TASK channel activity. |
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手法 | EM (単粒子) |
解像度 | 2.48 - 3.32 Å |
構造データ | EMDB-51158, PDB-9g9v: EMDB-51159, PDB-9g9w: EMDB-51160, PDB-9g9x: |
化合物 | ![]() ChemComp-Y01: ![]() ChemComp-K: |
由来 |
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![]() | MEMBRANE PROTEIN / K2P / potassium channel / ion channel |