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GSG1L-containing AMPA receptor complexes are defined by their spatiotemporal expression, native interactome and allosteric sites

Transmembrane AMPA receptor regulatory proteins (TARPs) and germ cell-specific gene 1-like protein (GSG1L) are claudin-type AMPA receptor (AMPAR) auxiliary subunits that profoundly regulate glutamatergic synapse strength and plasticity. While AMPAR-TARP complexes have been extensively studied, less...

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Autores principales: Perozzo, Amanda M., Schwenk, Jochen, Kamalova, Aichurok, Nakagawa, Terunaga, Fakler, Bernd, Bowie, Derek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603098/
https://www.ncbi.nlm.nih.gov/pubmed/37884493
http://dx.doi.org/10.1038/s41467-023-42517-7
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author Perozzo, Amanda M.
Schwenk, Jochen
Kamalova, Aichurok
Nakagawa, Terunaga
Fakler, Bernd
Bowie, Derek
author_facet Perozzo, Amanda M.
Schwenk, Jochen
Kamalova, Aichurok
Nakagawa, Terunaga
Fakler, Bernd
Bowie, Derek
author_sort Perozzo, Amanda M.
collection PubMed
description Transmembrane AMPA receptor regulatory proteins (TARPs) and germ cell-specific gene 1-like protein (GSG1L) are claudin-type AMPA receptor (AMPAR) auxiliary subunits that profoundly regulate glutamatergic synapse strength and plasticity. While AMPAR-TARP complexes have been extensively studied, less is known about GSG1L-containing AMPARs. Here, we show that GSG1L’s spatiotemporal expression, native interactome and allosteric sites are distinct. GSG1L generally expresses late during brain development in a region-specific manner, constituting about 5% of all AMPAR complexes in adulthood. While GSG1L can co-assemble with TARPs or cornichons (CNIHs), it also assembles as the sole auxiliary subunit. Unexpectedly, GSG1L acts through two discrete evolutionarily-conserved sites on the agonist-binding domain with a weak allosteric interaction at the TARP/KGK site to slow desensitization, and a stronger interaction at a different site that slows recovery from desensitization. Together, these distinctions help explain GSG1L’s evolutionary past and how it fulfills a unique signaling role within glutamatergic synapses.
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spelling pubmed-106030982023-10-28 GSG1L-containing AMPA receptor complexes are defined by their spatiotemporal expression, native interactome and allosteric sites Perozzo, Amanda M. Schwenk, Jochen Kamalova, Aichurok Nakagawa, Terunaga Fakler, Bernd Bowie, Derek Nat Commun Article Transmembrane AMPA receptor regulatory proteins (TARPs) and germ cell-specific gene 1-like protein (GSG1L) are claudin-type AMPA receptor (AMPAR) auxiliary subunits that profoundly regulate glutamatergic synapse strength and plasticity. While AMPAR-TARP complexes have been extensively studied, less is known about GSG1L-containing AMPARs. Here, we show that GSG1L’s spatiotemporal expression, native interactome and allosteric sites are distinct. GSG1L generally expresses late during brain development in a region-specific manner, constituting about 5% of all AMPAR complexes in adulthood. While GSG1L can co-assemble with TARPs or cornichons (CNIHs), it also assembles as the sole auxiliary subunit. Unexpectedly, GSG1L acts through two discrete evolutionarily-conserved sites on the agonist-binding domain with a weak allosteric interaction at the TARP/KGK site to slow desensitization, and a stronger interaction at a different site that slows recovery from desensitization. Together, these distinctions help explain GSG1L’s evolutionary past and how it fulfills a unique signaling role within glutamatergic synapses. Nature Publishing Group UK 2023-10-26 /pmc/articles/PMC10603098/ /pubmed/37884493 http://dx.doi.org/10.1038/s41467-023-42517-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Perozzo, Amanda M.
Schwenk, Jochen
Kamalova, Aichurok
Nakagawa, Terunaga
Fakler, Bernd
Bowie, Derek
GSG1L-containing AMPA receptor complexes are defined by their spatiotemporal expression, native interactome and allosteric sites
title GSG1L-containing AMPA receptor complexes are defined by their spatiotemporal expression, native interactome and allosteric sites
title_full GSG1L-containing AMPA receptor complexes are defined by their spatiotemporal expression, native interactome and allosteric sites
title_fullStr GSG1L-containing AMPA receptor complexes are defined by their spatiotemporal expression, native interactome and allosteric sites
title_full_unstemmed GSG1L-containing AMPA receptor complexes are defined by their spatiotemporal expression, native interactome and allosteric sites
title_short GSG1L-containing AMPA receptor complexes are defined by their spatiotemporal expression, native interactome and allosteric sites
title_sort gsg1l-containing ampa receptor complexes are defined by their spatiotemporal expression, native interactome and allosteric sites
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603098/
https://www.ncbi.nlm.nih.gov/pubmed/37884493
http://dx.doi.org/10.1038/s41467-023-42517-7
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