Surfaceome dynamics reveal proteostasis-independent reorganization of neuronal surface proteins during development and synaptic plasticity
Cell surface proteins contribute to neuronal development and activity-dependent synaptic plasticity. Here, the authors perform a time-resolved surfaceome analysis of developing primary neurons and in response to homeostatic synaptic scaling and chemical long-term potentiation (cLTP), revealing surfa...
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Nature Portfolio
2020
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oai:doaj.org-article:798a0222f1cc45678a4c20efbeb73d272021-12-02T18:37:17ZSurfaceome dynamics reveal proteostasis-independent reorganization of neuronal surface proteins during development and synaptic plasticity10.1038/s41467-020-18494-62041-1723https://doaj.org/article/798a0222f1cc45678a4c20efbeb73d272020-10-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-18494-6https://doaj.org/toc/2041-1723Cell surface proteins contribute to neuronal development and activity-dependent synaptic plasticity. Here, the authors perform a time-resolved surfaceome analysis of developing primary neurons and in response to homeostatic synaptic scaling and chemical long-term potentiation (cLTP), revealing surface proteome remodeling largely independent of global proteostasis.Marc van OostrumBenjamin CampbellCharlotte SengMaik MüllerSusanne tom DieckJacqueline HammerPatrick G. A. PedrioliCsaba FöldyShiva K. TyagarajanBernd WollscheidNature PortfolioarticleScienceQENNature Communications, Vol 11, Iss 1, Pp 1-16 (2020) |
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Science Q Marc van Oostrum Benjamin Campbell Charlotte Seng Maik Müller Susanne tom Dieck Jacqueline Hammer Patrick G. A. Pedrioli Csaba Földy Shiva K. Tyagarajan Bernd Wollscheid Surfaceome dynamics reveal proteostasis-independent reorganization of neuronal surface proteins during development and synaptic plasticity |
description |
Cell surface proteins contribute to neuronal development and activity-dependent synaptic plasticity. Here, the authors perform a time-resolved surfaceome analysis of developing primary neurons and in response to homeostatic synaptic scaling and chemical long-term potentiation (cLTP), revealing surface proteome remodeling largely independent of global proteostasis. |
format |
article |
author |
Marc van Oostrum Benjamin Campbell Charlotte Seng Maik Müller Susanne tom Dieck Jacqueline Hammer Patrick G. A. Pedrioli Csaba Földy Shiva K. Tyagarajan Bernd Wollscheid |
author_facet |
Marc van Oostrum Benjamin Campbell Charlotte Seng Maik Müller Susanne tom Dieck Jacqueline Hammer Patrick G. A. Pedrioli Csaba Földy Shiva K. Tyagarajan Bernd Wollscheid |
author_sort |
Marc van Oostrum |
title |
Surfaceome dynamics reveal proteostasis-independent reorganization of neuronal surface proteins during development and synaptic plasticity |
title_short |
Surfaceome dynamics reveal proteostasis-independent reorganization of neuronal surface proteins during development and synaptic plasticity |
title_full |
Surfaceome dynamics reveal proteostasis-independent reorganization of neuronal surface proteins during development and synaptic plasticity |
title_fullStr |
Surfaceome dynamics reveal proteostasis-independent reorganization of neuronal surface proteins during development and synaptic plasticity |
title_full_unstemmed |
Surfaceome dynamics reveal proteostasis-independent reorganization of neuronal surface proteins during development and synaptic plasticity |
title_sort |
surfaceome dynamics reveal proteostasis-independent reorganization of neuronal surface proteins during development and synaptic plasticity |
publisher |
Nature Portfolio |
publishDate |
2020 |
url |
https://doaj.org/article/798a0222f1cc45678a4c20efbeb73d27 |
work_keys_str_mv |
AT marcvanoostrum surfaceomedynamicsrevealproteostasisindependentreorganizationofneuronalsurfaceproteinsduringdevelopmentandsynapticplasticity AT benjamincampbell surfaceomedynamicsrevealproteostasisindependentreorganizationofneuronalsurfaceproteinsduringdevelopmentandsynapticplasticity AT charlotteseng surfaceomedynamicsrevealproteostasisindependentreorganizationofneuronalsurfaceproteinsduringdevelopmentandsynapticplasticity AT maikmuller surfaceomedynamicsrevealproteostasisindependentreorganizationofneuronalsurfaceproteinsduringdevelopmentandsynapticplasticity AT susannetomdieck surfaceomedynamicsrevealproteostasisindependentreorganizationofneuronalsurfaceproteinsduringdevelopmentandsynapticplasticity AT jacquelinehammer surfaceomedynamicsrevealproteostasisindependentreorganizationofneuronalsurfaceproteinsduringdevelopmentandsynapticplasticity AT patrickgapedrioli surfaceomedynamicsrevealproteostasisindependentreorganizationofneuronalsurfaceproteinsduringdevelopmentandsynapticplasticity AT csabafoldy surfaceomedynamicsrevealproteostasisindependentreorganizationofneuronalsurfaceproteinsduringdevelopmentandsynapticplasticity AT shivaktyagarajan surfaceomedynamicsrevealproteostasisindependentreorganizationofneuronalsurfaceproteinsduringdevelopmentandsynapticplasticity AT berndwollscheid surfaceomedynamicsrevealproteostasisindependentreorganizationofneuronalsurfaceproteinsduringdevelopmentandsynapticplasticity |
_version_ |
1718377805922697216 |