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PMID: 16888141 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

N- to C-terminal SNARE complex assembly promotes rapid membrane fusion.

Science (New York, N.Y.) ·Vol. 313 ·No. 5787 ·2006-08-04 ·Pages 673-6

Pobbati AV, Stein A, Fasshauer D

Abstract

Assembly of the soluble N-ethylmaleimide-sensitive factor attachment protein receptors (SNAREs) syntaxin 1, SNAP-25, and synaptobrevin 2 is thought to be the driving force for the exocytosis of synaptic vesicles. However, whereas exocytosis is triggered at a millisecond time scale, the SNARE-mediated fusion of liposomes requires hours for completion, which challenges the idea of a key role for SNAREs in the final steps of exocytosis. We found that liposome fusion was dramatically accelerated when a stabilized syntaxin/SNAP-25 acceptor complex was used. Thus, SNAREs do have the capacity to execute fusion at a speed required for neuronal secretion, demonstrating that the maintenance of acceptor complexes is a critical step in biological fusion reactions.

MeSH Terms
Amino Acid Sequence Animals Binding Sites Circular Dichroism Dimerization Exocytosis Liposomes/chemistry Membrane Fusion Molecular Sequence Data Peptide Fragments/chemistry,metabolism Protein Binding Protein Folding Protein Structure, Secondary Qa-SNARE Proteins/chemistry,metabolism R-SNARE Proteins/chemistry,metabolism Rats Synaptosomal-Associated Protein 25/chemistry,metabolism
Chemicals
Liposomes Peptide Fragments Qa-SNARE Proteins R-SNARE Proteins Synaptosomal-Associated Protein 25
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Pobbati Ajaybabu V
Department of Neurobiology, Max-Planck-Institute for Biophysical Chemistry, Am Fassberg 11, 37077 Göttingen, Germany.
Stein Alexander
Fasshauer Dirk
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
1095-9203
Published
2006-08-04
Pages
673-6
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIGMS NIH HHS · P01 GM072694 · United States
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