Literature DB >> 26891027

The dynamic AMPA receptor extracellular region: a platform for synaptic protein interactions.

J García-Nafría1, B Herguedas1, J F Watson1, I H Greger2.   

Abstract

AMPA receptors (AMPARs) are glutamate-gated cation channels that mediate fast excitatory neurotransmission and synaptic plasticity. Structures of GluA2 homotetramers in distinct functional states, together with simulations, emphasise the loose architecture of the AMPAR extracellular region (ECR). The ECR encompasses ∼80% of the receptor, and consists of the membrane-distal N-terminal domain (NTD) and ligand-binding domain (LBD), which is fused to the ion channel domain. Minimal contacts within and between layers, together with flexible peptide linkers connecting these three domains give rise to an organisation capable of dynamic rearrangements. This building plan is uniquely suited to engage interaction partners in the crowded environment of synapses, permitting the formation of new binding sites and the loss of existing ones. ECR motions are thereby expected to impact signalling as well as synaptic anchorage and may thereby influence AMPAR clustering during synaptic plasticity.
© 2016 MRC Laboratory of Molecular Biology. The Journal of Physiology © 2016 The Physiological Society.

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Year:  2016        PMID: 26891027      PMCID: PMC5043031          DOI: 10.1113/JP271844

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  81 in total

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Review 3.  Glutamate receptor dynamics in dendritic microdomains.

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4.  Submillisecond AMPA receptor-mediated signaling at a principal neuron-interneuron synapse.

Authors:  J R Geiger; J Lübke; A Roth; M Frotscher; P Jonas
Journal:  Neuron       Date:  1997-06       Impact factor: 17.173

5.  GRIP1 interlinks N-cadherin and AMPA receptors at vesicles to promote combined cargo transport into dendrites.

Authors:  Frank F Heisler; Han Kyu Lee; Kira V Gromova; Yvonne Pechmann; Beate Schurek; Laura Ruschkies; Markus Schroeder; Michaela Schweizer; Matthias Kneussel
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8.  Crystal structure of a heterotetrameric NMDA receptor ion channel.

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Journal:  Science       Date:  2014-05-30       Impact factor: 47.728

9.  Molecular dissection of the interaction between the AMPA receptor and cornichon homolog-3.

Authors:  Natalie F Shanks; Ondrej Cais; Tomohiko Maruo; Jeffrey N Savas; Elena I Zaika; Caleigh M Azumaya; John R Yates; Ingo Greger; Terunaga Nakagawa
Journal:  J Neurosci       Date:  2014-09-03       Impact factor: 6.167

10.  NMDA receptor structures reveal subunit arrangement and pore architecture.

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Review 2.  The Challenge of Interpreting Glutamate-Receptor Ion-Channel Structures.

Authors:  Mark L Mayer
Journal:  Biophys J       Date:  2017-08-24       Impact factor: 4.033

Review 3.  Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels.

Authors:  Kasper B Hansen; Lonnie P Wollmuth; Derek Bowie; Hiro Furukawa; Frank S Menniti; Alexander I Sobolevsky; Geoffrey T Swanson; Sharon A Swanger; Ingo H Greger; Terunaga Nakagawa; Chris J McBain; Vasanthi Jayaraman; Chian-Ming Low; Mark L Dell'Acqua; Jeffrey S Diamond; Chad R Camp; Riley E Perszyk; Hongjie Yuan; Stephen F Traynelis
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Journal:  J Biol Chem       Date:  2018-10-17       Impact factor: 5.157

6.  Structure and organization of heteromeric AMPA-type glutamate receptors.

Authors:  Beatriz Herguedas; Javier García-Nafría; Ondrej Cais; Rafael Fernández-Leiro; James Krieger; Hinze Ho; Ingo H Greger
Journal:  Science       Date:  2016-03-10       Impact factor: 47.728

7.  Structural Mechanisms of Gating in Ionotropic Glutamate Receptors.

Authors:  Edward C Twomey; Alexander I Sobolevsky
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Review 8.  AMPA receptor structure and auxiliary subunits.

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Journal:  J Physiol       Date:  2020-02-18       Impact factor: 5.182

9.  Unitary Properties of AMPA Receptors with Reduced Desensitization.

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Review 10.  Positive AMPA receptor modulation in the treatment of neuropsychiatric disorders: A long and winding road.

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