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Scaffold remodeling in space and time controls synaptic transmission

Scaffolding proteins that are associated with glutamate receptors in dendritic spines govern the location and function of receptors to control synaptic transmission. Unraveling the spatio-temporal dynamics of protein-protein interactions within components of the scaffolding complex will bring to lig...

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Detalles Bibliográficos
Autores principales: Perroy, Julie, Moutin, Enora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3383718/
https://www.ncbi.nlm.nih.gov/pubmed/22754626
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author Perroy, Julie
Moutin, Enora
author_facet Perroy, Julie
Moutin, Enora
author_sort Perroy, Julie
collection PubMed
description Scaffolding proteins that are associated with glutamate receptors in dendritic spines govern the location and function of receptors to control synaptic transmission. Unraveling the spatio-temporal dynamics of protein-protein interactions within components of the scaffolding complex will bring to light the function of these interactions. Combining bioluminescence resonance energy transfer (BRET) imaging to electrophysiological recordings, we have recently shown that GKAP, a core protein of the scaffolding complex, interacts with DLC2, a protein associated with molecular motors. Synaptic activity-induced GKAP-DLC2 interaction in spines stabilizes the scaffolding complex and enhances the NMDA currents. Interestingly, this work placed emphasis on the bioarchitectural dependence of protein-protein interaction dynamics. Depending on physiological conditions, the modulation in space and time of protein-protein interaction is acutely regulated, engendering a subtle control of synaptic transmission in the state of the individual synapse.
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spelling pubmed-33837182012-06-29 Scaffold remodeling in space and time controls synaptic transmission Perroy, Julie Moutin, Enora Bioarchitecture Commentary Scaffolding proteins that are associated with glutamate receptors in dendritic spines govern the location and function of receptors to control synaptic transmission. Unraveling the spatio-temporal dynamics of protein-protein interactions within components of the scaffolding complex will bring to light the function of these interactions. Combining bioluminescence resonance energy transfer (BRET) imaging to electrophysiological recordings, we have recently shown that GKAP, a core protein of the scaffolding complex, interacts with DLC2, a protein associated with molecular motors. Synaptic activity-induced GKAP-DLC2 interaction in spines stabilizes the scaffolding complex and enhances the NMDA currents. Interestingly, this work placed emphasis on the bioarchitectural dependence of protein-protein interaction dynamics. Depending on physiological conditions, the modulation in space and time of protein-protein interaction is acutely regulated, engendering a subtle control of synaptic transmission in the state of the individual synapse. Landes Bioscience 2012-02-01 /pmc/articles/PMC3383718/ /pubmed/22754626 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Commentary
Perroy, Julie
Moutin, Enora
Scaffold remodeling in space and time controls synaptic transmission
title Scaffold remodeling in space and time controls synaptic transmission
title_full Scaffold remodeling in space and time controls synaptic transmission
title_fullStr Scaffold remodeling in space and time controls synaptic transmission
title_full_unstemmed Scaffold remodeling in space and time controls synaptic transmission
title_short Scaffold remodeling in space and time controls synaptic transmission
title_sort scaffold remodeling in space and time controls synaptic transmission
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3383718/
https://www.ncbi.nlm.nih.gov/pubmed/22754626
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