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2QS3

Crystal structure of the GluR5 ligand binding core dimer in complex with UBP316 at 1.76 Angstroms resolution

2QS3 の概要
エントリーDOI10.2210/pdb2qs3/pdb
関連するPDBエントリー1TXF 2F34 2F35 2F36 2QS1 2QS2 2QS4
分子名称Glutamate receptor, ionotropic kainate 1, CHLORIDE ION, PENTAETHYLENE GLYCOL, ... (5 entities in total)
機能のキーワードmembrane protein, cell junction, glycoprotein, ion transport, ionic channel, phosphorylation, postsynaptic cell membrane, receptor, rna editing, synapse, transmembrane, transport
由来する生物種Rattus norvegicus (rat)
詳細
細胞内の位置Cell membrane; Multi-pass membrane protein: P22756
タンパク質・核酸の鎖数2
化学式量合計59829.42
構造登録者
Alushin, G.M.,Jane, D.E.,Mayer, M.L. (登録日: 2007-07-30, 公開日: 2008-08-05, 最終更新日: 2023-08-30)
主引用文献Dargan, S.L.,Clarke, V.R.,Alushin, G.M.,Sherwood, J.L.,Nistico, R.,Bortolotto, Z.A.,Ogden, A.M.,Bleakman, D.,Doherty, A.J.,Lodge, D.,Mayer, M.L.,Fitzjohn, S.M.,Jane, D.E.,Collingridge, G.L.
ACET is a highly potent and specific kainate receptor antagonist: characterisation and effects on hippocampal mossy fibre function.
Neuropharmacology, 56:121-130, 2009
Cited by
PubMed Abstract: Kainate receptors (KARs) are involved in both NMDA receptor-independent long-term potentiation (LTP) and synaptic facilitation at mossy fibre synapses in the CA3 region of the hippocampus. However, the identity of the KAR subtypes involved remains controversial. Here we used a highly potent and selective GluK1 (formerly GluR5) antagonist (ACET) to elucidate roles of GluK1-containing KARs in these synaptic processes. We confirmed that ACET is an extremely potent GluK1 antagonist, with a Kb value of 1.4+/-0.2 nM. In contrast, ACET was ineffective at GluK2 (formerly GluR6) receptors at all concentrations tested (up to 100 microM) and had no effect at GluK3 (formerly GluR7) when tested at 1 microM. The X-ray crystal structure of ACET bound to the ligand binding core of GluK1 was similar to the UBP310-GluK1 complex. In the CA1 region of hippocampal slices, ACET was effective at blocking the depression of both fEPSPs and monosynaptically evoked GABAergic transmission induced by ATPA, a GluK1 selective agonist. In the CA3 region of the hippocampus, ACET blocked the induction of NMDA receptor-independent mossy fibre LTP. To directly investigate the role of pre-synaptic GluK1-containing KARs we combined patch-clamp electrophysiology and 2-photon microscopy to image Ca2+ dynamics in individual giant mossy fibre boutons. ACET consistently reduced short-term facilitation of pre-synaptic calcium transients induced by 5 action potentials evoked at 20-25Hz. Taken together our data provide further evidence for a physiological role of GluK1-containing KARs in synaptic facilitation and LTP induction at mossy fibre-CA3 synapses.
PubMed: 18789344
DOI: 10.1016/j.neuropharm.2008.08.016
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.76 Å)
構造検証レポート
Validation report summary of 2qs3
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2026-03-04に公開中

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