8AYM
Resting state GluA1/A2 AMPA receptor in complex with TARP gamma 8 and ligand JNJ-55511118
8AYM の概要
| エントリーDOI | 10.2210/pdb8aym/pdb |
| EMDBエントリー | 15716 |
| 分子名称 | Voltage-dependent calcium channel gamma-8 subunit, Isoform Flip of Glutamate receptor 1, Isoform Flip of Glutamate receptor 2, ... (8 entities in total) |
| 機能のキーワード | ampar, ion channels, neurotransmission, membrane protein |
| 由来する生物種 | Rattus norvegicus (Norway rat) 詳細 |
| タンパク質・核酸の鎖数 | 6 |
| 化学式量合計 | 496127.81 |
| 構造登録者 | Zhang, D.,Lape, R.,Shaikh, S.,Kohegyi, B.,Watson, J.F.,Cais, O.,Nakagawa, T.,Greger, I.H. (登録日: 2022-09-02, 公開日: 2023-04-19, 最終更新日: 2024-11-06) |
| 主引用文献 | Zhang, D.,Lape, R.,Shaikh, S.A.,Kohegyi, B.K.,Watson, J.F.,Cais, O.,Nakagawa, T.,Greger, I.H. Modulatory mechanisms of TARP gamma 8-selective AMPA receptor therapeutics. Nat Commun, 14:1659-1659, 2023 Cited by PubMed Abstract: AMPA glutamate receptors (AMPARs) mediate excitatory neurotransmission throughout the brain. Their signalling is uniquely diversified by brain region-specific auxiliary subunits, providing an opportunity for the development of selective therapeutics. AMPARs associated with TARP γ8 are enriched in the hippocampus, and are targets of emerging anti-epileptic drugs. To understand their therapeutic activity, we determined cryo-EM structures of the GluA1/2-γ8 receptor associated with three potent, chemically diverse ligands. We find that despite sharing a lipid-exposed and water-accessible binding pocket, drug action is differentially affected by binding-site mutants. Together with patch-clamp recordings and MD simulations we also demonstrate that ligand-triggered reorganisation of the AMPAR-TARP interface contributes to modulation. Unexpectedly, one ligand (JNJ-61432059) acts bifunctionally, negatively affecting GluA1 but exerting positive modulatory action on GluA2-containing AMPARs, in a TARP stoichiometry-dependent manner. These results further illuminate the action of TARPs, demonstrate the sensitive balance between positive and negative modulatory action, and provide a mechanistic platform for development of both positive and negative selective AMPAR modulators. PubMed: 36966141DOI: 10.1038/s41467-023-37259-5 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (3.3 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード






