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8UG5

Caenorhabditis elegans Otopetrin 8 (CeOtop8) in pH 5.0

8UG5 の概要
エントリーDOI10.2210/pdb8ug5/pdb
EMDBエントリー42214
分子名称Otopetrin-2 (1 entity in total)
機能のキーワードproton channel, otop, c.elegans, otopetrin, membrane protein
由来する生物種Caenorhabditis elegans
タンパク質・核酸の鎖数2
化学式量合計139583.02
構造登録者
Gan, N.,Jiang, Y. (登録日: 2023-10-05, 公開日: 2024-08-21, 最終更新日: 2024-10-16)
主引用文献Gan, N.,Zeng, W.,Han, Y.,Chen, Q.,Jiang, Y.
Structural mechanism of proton conduction in otopetrin proton channel.
Nat Commun, 15:7250-7250, 2024
Cited by
PubMed Abstract: The otopetrin (OTOP) proteins were recently characterized as extracellular proton-activated proton channels. Several recent OTOP channel structures demonstrated that the channels form a dimer with each subunit adopting a double-barrel architecture. However, the structural mechanisms underlying some basic functional properties of the OTOP channels remain unresolved, including extracellular pH activation, proton conducting pathway, and rapid desensitization. In this study, we performed structural and functional characterization of the Caenorhabditis elegans OTOP8 (CeOTOP8) and mouse OTOP2 (mOTOP2) and illuminated a set of conformational changes related to the proton-conducting process in OTOP. The structures of CeOTOP8 reveal the conformational change at the N-terminal part of TM12 that renders the channel in a transiently proton-transferring state, elucidating an inter-barrel, Glu/His-bridged proton passage within each subunit. The structures of mOTOP2 reveal the conformational change at the N-terminal part of TM6 that exposes the central glutamate to the extracellular solution for protonation. In addition, the structural comparison between CeOTOP8 and mOTOP2, along with the structure-based mutagenesis, demonstrates that an inter-subunit movement at the OTOP channel dimer interface plays a central role in regulating channel activity. Combining the structural information from both channels, we propose a working model describing the multi-step conformational changes during the proton conducting process.
PubMed: 39179582
DOI: 10.1038/s41467-024-51803-x
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (2.91 Å)
構造検証レポート
Validation report summary of 8ug5
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-05-28に公開中

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