t-SNARE Transmembrane Domain Clustering Modulates Lipid Organization and Membrane Curvature
Author(s) -
Satyan Sharma,
Manfred Lindau
Publication year - 2017
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.7b10677
Subject(s) - chemistry , membrane curvature , snap25 , lipid bilayer fusion , snare complex , transmembrane domain , vesicle , syntaxin , transmembrane protein , biophysics , membrane , microbiology and biotechnology , synaptic vesicle , biochemistry , receptor , biology
The t-SNARE complex plays a central role in neuronal fusion. Its components, syntaxin-1 and SNAP25, are largely present in individual clusters and partially colocalize at the presumptive fusion site. How these protein clusters modify local lipid composition and membrane morphology is largely unknown. In this work, using coarse-grained molecular dynamics, the transmembrane domains (TMDs) of t-SNARE complexes are shown to form aggregates leading to formation of lipid nanodomains, which are enriched in cholesterol, phosphatidylinositol 4,5-bisphosphate, and gangliosidic lipids. These nano-domains induce membrane curvature that would promote a closer contact between vesicle and plasma membrane.
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