8JIZ
Cryo-EM structure of GluN1-2A NMDAR in complex with human Fab5F6 in two fab bind conformation
8JIZ の概要
エントリーDOI | 10.2210/pdb8jiz/pdb |
EMDBエントリー | 36335 |
分子名称 | Glutamate receptor ionotropic, NMDA 2A, Glutamate receptor ionotropic, NMDA 1, Fab5F6 Heavy Chain, ... (6 entities in total) |
機能のキーワード | nmdar, autoimmune encephalitis, membrane protein |
由来する生物種 | Homo sapiens (human) 詳細 |
タンパク質・核酸の鎖数 | 8 |
化学式量合計 | 489768.21 |
構造登録者 | |
主引用文献 | Wang, H.,Xie, C.,Deng, B.,Ding, J.,Li, N.,Kou, Z.,Jin, M.,He, J.,Wang, Q.,Wen, H.,Zhang, J.,Zhou, Q.,Chen, S.,Chen, X.,Yuan, T.F.,Zhu, S. Structural basis for antibody-mediated NMDA receptor clustering and endocytosis in autoimmune encephalitis. Nat.Struct.Mol.Biol., 2024 Cited by PubMed Abstract: Antibodies against N-methyl-D-aspartate receptors (NMDARs) are most frequently detected in persons with autoimmune encephalitis (AE) and used as diagnostic biomarkers. Elucidating the structural basis of monoclonal antibody (mAb) binding to NMDARs would facilitate the development of targeted therapy for AE. Here, we reconstructed nanodiscs containing green fluorescent protein-fused NMDARs to label and sort individual immune B cells from persons with AE and further cloned and identified mAbs against NMDARs. This allowed cryo-electron microscopy analysis of NMDAR-Fab complexes, revealing that autoantibodies bind to the R1 lobe of the N-terminal domain of the GluN1 subunit. Small-angle X-ray scattering studies demonstrated NMDAR-mAb stoichiometry of 2:1 or 1:2, structurally suitable for mAb-induced clustering and endocytosis of NMDARs. Importantly, these mAbs reduced the surface NMDARs and NMDAR-mediated currents, without tonically affecting NMDAR channel gating. These structural and functional findings imply that the design of neutralizing antibody binding to the R1 lobe of NMDARs represents a potential therapy for AE treatment. PubMed: 39227720DOI: 10.1038/s41594-024-01387-3 主引用文献が同じPDBエントリー |
実験手法 | ELECTRON MICROSCOPY (3.8 Å) |
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