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Yorodumi- PDB-8ss7: Structure of AMPA receptor GluA2 complex with auxiliary subunits ... -
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Basic information
| Entry | Database: PDB / ID: 8ss7 | |||||||||||||||
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| Title | Structure of AMPA receptor GluA2 complex with auxiliary subunits TARP gamma-5 and cornichon-2 bound to competitive antagonist ZK, channel blocker spermidine and antiepileptic drug perampanel (closed state) | |||||||||||||||
|  Components | 
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|  Keywords | SIGNALING PROTEIN / AMPA receptor / spermidine / perampanel / cornichon-2 | |||||||||||||||
| Function / homology |  Function and homology information postsynaptic neurotransmitter receptor diffusion trapping / regulation of AMPA receptor activity / channel regulator activity / Cargo concentration in the ER / COPII-mediated vesicle transport / spine synapse / dendritic spine neck / dendritic spine head / cellular response to amine stimulus / perisynaptic space ...postsynaptic neurotransmitter receptor diffusion trapping / regulation of AMPA receptor activity / channel regulator activity / Cargo concentration in the ER / COPII-mediated vesicle transport / spine synapse / dendritic spine neck / dendritic spine head / cellular response to amine stimulus / perisynaptic space / Activation of AMPA receptors / ligand-gated monoatomic cation channel activity / AMPA glutamate receptor activity / transmission of nerve impulse / response to lithium ion / Trafficking of GluR2-containing AMPA receptors / kainate selective glutamate receptor activity / AMPA glutamate receptor complex / cellular response to glycine / extracellularly glutamate-gated ion channel activity / immunoglobulin binding / asymmetric synapse / ionotropic glutamate receptor complex / conditioned place preference / regulation of receptor recycling / glutamate receptor binding / Unblocking of NMDA receptors, glutamate binding and activation / positive regulation of synaptic transmission / positive regulation of synaptic transmission, glutamatergic / regulation of synaptic transmission, glutamatergic / voltage-gated calcium channel activity / response to fungicide / cytoskeletal protein binding / glutamate-gated receptor activity / vesicle-mediated transport / regulation of long-term synaptic depression / extracellular ligand-gated monoatomic ion channel activity / cellular response to brain-derived neurotrophic factor stimulus / presynaptic active zone membrane / glutamate-gated calcium ion channel activity / somatodendritic compartment / dendrite membrane / ionotropic glutamate receptor binding / endoplasmic reticulum-Golgi intermediate compartment membrane / ligand-gated monoatomic ion channel activity involved in regulation of presynaptic membrane potential / ionotropic glutamate receptor signaling pathway / dendrite cytoplasm / synaptic membrane / dendritic shaft / SNARE binding / transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic membrane potential / synaptic transmission, glutamatergic / PDZ domain binding / protein tetramerization / establishment of protein localization / ER to Golgi transport vesicle membrane / postsynaptic density membrane / cerebral cortex development / modulation of chemical synaptic transmission / receptor internalization / Schaffer collateral - CA1 synapse / terminal bouton / synaptic vesicle / synaptic vesicle membrane / presynapse / signaling receptor activity / amyloid-beta binding / presynaptic membrane / growth cone / scaffold protein binding / perikaryon / chemical synaptic transmission / dendritic spine / postsynaptic membrane / neuron projection / postsynaptic density / signaling receptor binding / axon / external side of plasma membrane / neuronal cell body / dendrite / synapse / endoplasmic reticulum membrane / protein kinase binding / protein-containing complex binding / glutamatergic synapse / cell surface / endoplasmic reticulum / protein-containing complex / identical protein binding / membrane / plasma membrane Similarity search - Function | |||||||||||||||
| Biological species |   Rattus norvegicus (Norway rat)  Homo sapiens (human) | |||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 2.76 Å | |||||||||||||||
|  Authors | Gangwar, S.P. / Yen, L.Y. / Yelshanskaya, M.V. / Sobolevsky, A.I. | |||||||||||||||
| Funding support |  United States, 4items 
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|  Citation |  Journal: Nat Struct Mol Biol / Year: 2023 Title: Modulation of GluA2-γ5 synaptic complex desensitization, polyamine block and antiepileptic perampanel inhibition by auxiliary subunit cornichon-2. Authors: Shanti Pal Gangwar / Laura Y Yen / Maria V Yelshanskaya / Aryeh Korman / Drew R Jones / Alexander I Sobolevsky /  Abstract: Synaptic complexes of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors (AMPARs) with auxiliary subunits mediate most excitatory neurotransmission and can be targeted to treat ...Synaptic complexes of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors (AMPARs) with auxiliary subunits mediate most excitatory neurotransmission and can be targeted to treat neuropsychiatric and neurological disorders, including epilepsy. Here we present cryogenic-electron microscopy structures of rat GluA2 AMPAR complexes with inhibitory mouse γ5 and potentiating human cornichon-2 (CNIH2) auxiliary subunits. CNIH2 appears to destabilize the desensitized state of the complex by reducing the separation of the upper lobes in ligand-binding domain dimers. At the same time, CNIH2 stabilizes binding of polyamine spermidine to the selectivity filter of the closed ion channel. Nevertheless, CNIH2, and to a lesser extent γ5, attenuate polyamine block of the open channel and reduce the potency of the antiepileptic drug perampanel that inhibits the synaptic complex allosterically by binding to sites in the ion channel extracellular collar. These findings illustrate the fine-tuning of synaptic complex structure and function in an auxiliary subunit-dependent manner, which is critical for the study of brain region-specific neurotransmission and design of therapeutics for disease treatment. | |||||||||||||||
| History | 
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- Structure visualization
Structure visualization
| Structure viewer | Molecule:  Molmil  Jmol/JSmol | 
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| PDBx/mmCIF format |  8ss7.cif.gz | 478 KB | Display |  PDBx/mmCIF format | 
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| PDB format |  pdb8ss7.ent.gz | 368.6 KB | Display |  PDB format | 
| PDBx/mmJSON format |  8ss7.json.gz | Tree view |  PDBx/mmJSON format | |
| Others |  Other downloads | 
-Validation report
| Summary document |  8ss7_validation.pdf.gz | 3 MB | Display |  wwPDB validaton report | 
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| Full document |  8ss7_full_validation.pdf.gz | 3.1 MB | Display | |
| Data in XML |  8ss7_validation.xml.gz | 105.5 KB | Display | |
| Data in CIF |  8ss7_validation.cif.gz | 138.9 KB | Display | |
| Arichive directory |  https://data.pdbj.org/pub/pdb/validation_reports/ss/8ss7  ftp://data.pdbj.org/pub/pdb/validation_reports/ss/8ss7 | HTTPS FTP | 
-Related structure data
| Related structure data |  40746MC  8ss2C  8ss3C  8ss4C  8ss5C  8ss6C  8ss8C  8ss9C  8ssaC  8ssbC M: map data used to model this data C: citing same article ( | 
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| Similar structure data | Similarity search - Function & homology  F&H Search | 
- Links
Links
- Assembly
Assembly
| Deposited unit |  
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| 1 | 
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- Components
Components
-Protein , 2 types, 6 molecules ABCDEF     
| #1: Protein | Mass: 114978.859 Da / Num. of mol.: 4 Source method: isolated from a genetically manipulated source Source: (gene. exp.)   Rattus norvegicus (Norway rat) / Gene: Gria2, Glur2, Cacng5 / Plasmid: pEG BacMam / Cell line (production host): HEK293S-GnTi / Production host:  Homo sapiens (human) / References: UniProt: P19491, UniProt: Q8VHW8 #2: Protein | Mass: 18948.420 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.)  Homo sapiens (human) / Cell line: HEK293S-GnTi / Gene: CNIH2, CNIL / Cell line (production host): HEK293S-GnTi / Production host:  Homo sapiens (human) / References: UniProt: Q6PI25 | 
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-Non-polymers , 6 types, 46 molecules 










| #3: Chemical | ChemComp-6ZP / #4: Chemical | ChemComp-ZK1 / {[ #5: Chemical | ChemComp-PCW / #6: Chemical | ChemComp-CLR / #7: Chemical | ChemComp-NA / | #8: Chemical | ChemComp-SPD / |  | 
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-Details
| Has ligand of interest | Y | 
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| Has protein modification | Y | 
-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY | 
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| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction | 
- Sample preparation
Sample preparation
| Component | Name: GluA2-TARP gamma5-cornichon-2 / Type: COMPLEX Details: Structure of LBD-TMD of AMPA receptor GluA2 in complex with auxiliary subunits TARP gamma-5 and cornichon-2 bound to competitive antagonist ZK, channel blocker spermidine and antiepileptic ...Details: Structure of LBD-TMD of AMPA receptor GluA2 in complex with auxiliary subunits TARP gamma-5 and cornichon-2 bound to competitive antagonist ZK, channel blocker spermidine and antiepileptic drug perampanel (closed state) Entity ID: #1-#2 / Source: MULTIPLE SOURCES | |||||||||||||||||||||||||
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| Source (natural) | 
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| Source (recombinant) | 
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| Buffer solution | pH: 8 | |||||||||||||||||||||||||
| Buffer component | 
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| Specimen | Conc.: 4.5 mg/ml / Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES Details: Protein extracted and purified in detergent micelle | |||||||||||||||||||||||||
| Specimen support | Grid material: GOLD / Grid mesh size: 300 divisions/in. / Grid type: UltrAuFoil | |||||||||||||||||||||||||
| Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE / Humidity: 100 % / Chamber temperature: 277 K / Details: vitrification carried out in nitrogen atmosphere | 
- Electron microscopy imaging
Electron microscopy imaging
| Experimental equipment |  Model: Titan Krios / Image courtesy: FEI Company | 
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| Microscopy | Model: FEI TITAN KRIOS | 
| Electron gun | Electron source:  FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM | 
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 2000 nm / Nominal defocus min: 1000 nm / Cs: 2.7 mm / C2 aperture diameter: 100 µm | 
| Specimen holder | Cryogen: NITROGEN / Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER | 
| Image recording | Electron dose: 50 e/Å2 / Film or detector model: FEI FALCON IV (4k x 4k) | 
- Processing
Processing
| EM software | 
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||
| Symmetry | Point symmetry: C2 (2 fold cyclic) | ||||||||||||||||||||||||
| 3D reconstruction | Resolution: 2.76 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 126263 / Symmetry type: POINT | ||||||||||||||||||||||||
| Refine LS restraints | 
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