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PMID: 16845390 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Hemifusion arrest by complexin is relieved by Ca2+-synaptotagmin I.

Nature structural & molecular biology ·Vol. 13 ·No. 8 ·2006-08-00 ·Pages 748-50

Schaub JR, Lu X, Doneske B, Shin YK, McNew JA

Abstract

Synaptic transmission relies on an exquisitely orchestrated series of protein-protein interactions. Here we show that fusion driven by neuronal SNAREs is inhibited by the regulatory protein complexin. Furthermore, inner-leaflet mixing is strongly impaired relative to total lipid mixing, indicating that inhibition by complexin arrests fusion at hemifusion. When the calcium sensor synaptotagmin is added in the presence of calcium, inhibition by complexin is relieved and full fusion rapidly proceeds.

MeSH Terms
Adaptor Proteins, Vesicular Transport Animals Calcium/metabolism Drosophila Proteins/genetics,metabolism Escherichia coli/genetics Immunoprecipitation Liposomes/metabolism Membrane Fusion/physiology Mice Nerve Tissue Proteins/genetics,metabolism SNARE Proteins/genetics,metabolism Synaptic Transmission Synaptotagmin I/genetics,metabolism
Chemicals
Adaptor Proteins, Vesicular Transport Drosophila Proteins Liposomes Nerve Tissue Proteins SNARE Proteins Synaptotagmin I complexin I Calcium
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Schaub Johanna R
Department of Biochemistry and Cell Biology, Rice University, 6100 Main Street MS-140, Houston, Texas 77005, USA.
Lu Xiaobing
Doneske Blair
Shin Yeon-Kyun
McNew James A
Article Info
Journal
Nature structural & molecular biology
Abbr.
Nat Struct Mol Biol
ISSN
1545-9993
Published
2006-08-00
Epub
2006-00-16
Pages
748-50
Language
English
Region
United States
NLM ID
101186374
Subset
IM
Grants
NIGMS NIH HHS · GM051290 · United States
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