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The pre-synaptic fusion machinery

Here, we review recent insights into the neuronal presynaptic fusion machinery that releases neurotransmitter molecules into the synaptic cleft upon stimulation. The structure of the pre-fusion state of the SNARE/complexin-1/synaptotagmin-1 synaptic protein complex suggests a new model for the initi...

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Detalles Bibliográficos
Autores principales: Brunger, Axel T, Choi, Ucheor B, Lai, Ying, Leitz, Jeremy, White, Kristopher Ian, Zhou, Qiangjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6939388/
https://www.ncbi.nlm.nih.gov/pubmed/30986753
http://dx.doi.org/10.1016/j.sbi.2019.03.007
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author Brunger, Axel T
Choi, Ucheor B
Lai, Ying
Leitz, Jeremy
White, Kristopher Ian
Zhou, Qiangjun
author_facet Brunger, Axel T
Choi, Ucheor B
Lai, Ying
Leitz, Jeremy
White, Kristopher Ian
Zhou, Qiangjun
author_sort Brunger, Axel T
collection PubMed
description Here, we review recent insights into the neuronal presynaptic fusion machinery that releases neurotransmitter molecules into the synaptic cleft upon stimulation. The structure of the pre-fusion state of the SNARE/complexin-1/synaptotagmin-1 synaptic protein complex suggests a new model for the initiation of fast Ca(2+)-triggered membrane fusion. Functional studies have revealed roles of the essential factors Munc18 and Munc13, demonstrating that a part of their function involves the proper assembly of synaptic protein complexes. Near-atomic resolution structures of the NSF/αSNAP/SNARE complex provide first glimpses of the molecular machinery that disassembles the SNARE complex during the synaptic vesicle cycle. These structures show how this machinery captures the SNARE substrate and provide clues as to a possible processing mechanism.
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spelling pubmed-69393882020-01-02 The pre-synaptic fusion machinery Brunger, Axel T Choi, Ucheor B Lai, Ying Leitz, Jeremy White, Kristopher Ian Zhou, Qiangjun Curr Opin Struct Biol Article Here, we review recent insights into the neuronal presynaptic fusion machinery that releases neurotransmitter molecules into the synaptic cleft upon stimulation. The structure of the pre-fusion state of the SNARE/complexin-1/synaptotagmin-1 synaptic protein complex suggests a new model for the initiation of fast Ca(2+)-triggered membrane fusion. Functional studies have revealed roles of the essential factors Munc18 and Munc13, demonstrating that a part of their function involves the proper assembly of synaptic protein complexes. Near-atomic resolution structures of the NSF/αSNAP/SNARE complex provide first glimpses of the molecular machinery that disassembles the SNARE complex during the synaptic vesicle cycle. These structures show how this machinery captures the SNARE substrate and provide clues as to a possible processing mechanism. 2019-04-12 2019-02 /pmc/articles/PMC6939388/ /pubmed/30986753 http://dx.doi.org/10.1016/j.sbi.2019.03.007 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Brunger, Axel T
Choi, Ucheor B
Lai, Ying
Leitz, Jeremy
White, Kristopher Ian
Zhou, Qiangjun
The pre-synaptic fusion machinery
title The pre-synaptic fusion machinery
title_full The pre-synaptic fusion machinery
title_fullStr The pre-synaptic fusion machinery
title_full_unstemmed The pre-synaptic fusion machinery
title_short The pre-synaptic fusion machinery
title_sort pre-synaptic fusion machinery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6939388/
https://www.ncbi.nlm.nih.gov/pubmed/30986753
http://dx.doi.org/10.1016/j.sbi.2019.03.007
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