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Real-Time Visualization of Complexin During Single Exocytic Events

Understanding the fundamental role of SNARE complexes in membrane fusion requires knowledge of the spatiotemporal dynamics of their assembly. To this end, we visualized complexin (cplx), a cytosolic protein that binds assembled SNARE complexes, during single exocytic events in live cells. We show th...

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Detalles Bibliográficos
Autores principales: An, Seong J., Grabner, Chad P., Zenisek, David
Formato: Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2860691/
https://www.ncbi.nlm.nih.gov/pubmed/20383135
http://dx.doi.org/10.1038/nn.2532
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author An, Seong J.
Grabner, Chad P.
Zenisek, David
author_facet An, Seong J.
Grabner, Chad P.
Zenisek, David
author_sort An, Seong J.
collection PubMed
description Understanding the fundamental role of SNARE complexes in membrane fusion requires knowledge of the spatiotemporal dynamics of their assembly. To this end, we visualized complexin (cplx), a cytosolic protein that binds assembled SNARE complexes, during single exocytic events in live cells. We show that cplx appears briefly during full fusion. However, a truncated version of cplx containing only the SNARE-complex binding region persists at fusion sites for seconds and causes fusion to be transient. Resealing pores with the mutant cplx only partially release transmitter and lipid probes, indicating they are narrow and not purely lipidic in structure. Depletion of cplx similarly causes secretory cargo to be retained. Thus, complexin is recruited at a late step in exocytosis and modulates fusion pores composed of SNARE complexes.
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spelling pubmed-28606912010-11-01 Real-Time Visualization of Complexin During Single Exocytic Events An, Seong J. Grabner, Chad P. Zenisek, David Nat Neurosci Article Understanding the fundamental role of SNARE complexes in membrane fusion requires knowledge of the spatiotemporal dynamics of their assembly. To this end, we visualized complexin (cplx), a cytosolic protein that binds assembled SNARE complexes, during single exocytic events in live cells. We show that cplx appears briefly during full fusion. However, a truncated version of cplx containing only the SNARE-complex binding region persists at fusion sites for seconds and causes fusion to be transient. Resealing pores with the mutant cplx only partially release transmitter and lipid probes, indicating they are narrow and not purely lipidic in structure. Depletion of cplx similarly causes secretory cargo to be retained. Thus, complexin is recruited at a late step in exocytosis and modulates fusion pores composed of SNARE complexes. 2010-04-11 2010-05 /pmc/articles/PMC2860691/ /pubmed/20383135 http://dx.doi.org/10.1038/nn.2532 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
An, Seong J.
Grabner, Chad P.
Zenisek, David
Real-Time Visualization of Complexin During Single Exocytic Events
title Real-Time Visualization of Complexin During Single Exocytic Events
title_full Real-Time Visualization of Complexin During Single Exocytic Events
title_fullStr Real-Time Visualization of Complexin During Single Exocytic Events
title_full_unstemmed Real-Time Visualization of Complexin During Single Exocytic Events
title_short Real-Time Visualization of Complexin During Single Exocytic Events
title_sort real-time visualization of complexin during single exocytic events
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2860691/
https://www.ncbi.nlm.nih.gov/pubmed/20383135
http://dx.doi.org/10.1038/nn.2532
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