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The Sybtraps: Control of Synaptobrevin Traffic by Synaptophysin, α-Synuclein and AP-180

Synaptobrevin II (sybII) is a key fusogenic molecule on synaptic vesicles (SVs) therefore the active maintenance of both its conformation and location in sufficient numbers on this organelle is critical in both mediating and sustaining neurotransmitter release. Recently three proteins have been iden...

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Autores principales: Gordon, Sarah L, Cousin, Michael A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons A/S 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992847/
https://www.ncbi.nlm.nih.gov/pubmed/24279465
http://dx.doi.org/10.1111/tra.12140
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author Gordon, Sarah L
Cousin, Michael A
author_facet Gordon, Sarah L
Cousin, Michael A
author_sort Gordon, Sarah L
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description Synaptobrevin II (sybII) is a key fusogenic molecule on synaptic vesicles (SVs) therefore the active maintenance of both its conformation and location in sufficient numbers on this organelle is critical in both mediating and sustaining neurotransmitter release. Recently three proteins have been identified having key roles in the presentation, trafficking and retrieval of sybII during the fusion and endocytosis of SVs. The nerve terminal protein α-synuclein catalyses sybII entry into SNARE complexes, whereas the monomeric adaptor protein AP-180 is required for sybII retrieval during SV endocytosis. Overarching these events is the tetraspan SV protein synaptophysin, which is a major sybII interaction partner on the SV. This review will evaluate recent studies to propose working models for the control of sybII traffic by synaptophysin and other Sybtraps (sybII trafficking partners) and suggest how dysfunction in sybII traffic may contribute to human disease.
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spelling pubmed-39928472014-04-22 The Sybtraps: Control of Synaptobrevin Traffic by Synaptophysin, α-Synuclein and AP-180 Gordon, Sarah L Cousin, Michael A Traffic Review Synaptobrevin II (sybII) is a key fusogenic molecule on synaptic vesicles (SVs) therefore the active maintenance of both its conformation and location in sufficient numbers on this organelle is critical in both mediating and sustaining neurotransmitter release. Recently three proteins have been identified having key roles in the presentation, trafficking and retrieval of sybII during the fusion and endocytosis of SVs. The nerve terminal protein α-synuclein catalyses sybII entry into SNARE complexes, whereas the monomeric adaptor protein AP-180 is required for sybII retrieval during SV endocytosis. Overarching these events is the tetraspan SV protein synaptophysin, which is a major sybII interaction partner on the SV. This review will evaluate recent studies to propose working models for the control of sybII traffic by synaptophysin and other Sybtraps (sybII trafficking partners) and suggest how dysfunction in sybII traffic may contribute to human disease. John Wiley & Sons A/S 2014-03 2013-12-16 /pmc/articles/PMC3992847/ /pubmed/24279465 http://dx.doi.org/10.1111/tra.12140 Text en © 2013 The Authors. Traffic published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Gordon, Sarah L
Cousin, Michael A
The Sybtraps: Control of Synaptobrevin Traffic by Synaptophysin, α-Synuclein and AP-180
title The Sybtraps: Control of Synaptobrevin Traffic by Synaptophysin, α-Synuclein and AP-180
title_full The Sybtraps: Control of Synaptobrevin Traffic by Synaptophysin, α-Synuclein and AP-180
title_fullStr The Sybtraps: Control of Synaptobrevin Traffic by Synaptophysin, α-Synuclein and AP-180
title_full_unstemmed The Sybtraps: Control of Synaptobrevin Traffic by Synaptophysin, α-Synuclein and AP-180
title_short The Sybtraps: Control of Synaptobrevin Traffic by Synaptophysin, α-Synuclein and AP-180
title_sort sybtraps: control of synaptobrevin traffic by synaptophysin, α-synuclein and ap-180
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992847/
https://www.ncbi.nlm.nih.gov/pubmed/24279465
http://dx.doi.org/10.1111/tra.12140
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