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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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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. |
format | Online Article Text |
id | pubmed-10603098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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