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Drunken lipid membranes, not drunken SNARE proteins, promote fusion in a model of neurotransmitter release.


ABSTRACT: Alcohol affects many neuronal proteins that are upstream or down-stream of synaptic vesicle fusion and neurotransmitter release. Less well studied is alcohol's effect on the fusion machinery including SNARE proteins and lipid membranes. Using a SNARE-driven fusion assay we show that fusion probability is significantly increased at 0.4% v/v (68 mM) ethanol; but not with methanol up to 10%. Ethanol appears to act directly on membrane lipids since experiments focused on protein properties [circular dichroism spectrometry, site-directed fluorescence interference contrast (sdFLIC) microscopy, and vesicle docking results] showed no significant changes up to 5% ethanol, but a protein-free fusion assay also showed increased lipid membrane fusion rates with 0.4% ethanol. These data show that the effects of high physiological doses of ethanol on SNARE-driven fusion are mediated through ethanol's interaction with the lipid bilayer of membranes and not SNARE proteins, and that methanol affects lipid membranes and SNARE proteins only at high doses.

SUBMITTER: Coffman RE 

PROVIDER: S-EPMC9614348 | biostudies-literature | 2022

REPOSITORIES: biostudies-literature

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Drunken lipid membranes, not drunken SNARE proteins, promote fusion in a model of neurotransmitter release.

Coffman Robert E RE   Kraichely Katelyn N KN   Kreutzberger Alex J B AJB   Kiessling Volker V   Tamm Lukas K LK   Woodbury Dixon J DJ  

Frontiers in molecular neuroscience 20221014


Alcohol affects many neuronal proteins that are upstream or down-stream of synaptic vesicle fusion and neurotransmitter release. Less well studied is alcohol's effect on the fusion machinery including SNARE proteins and lipid membranes. Using a SNARE-driven fusion assay we show that fusion probability is significantly increased at 0.4% v/v (68 mM) ethanol; but not with methanol up to 10%. Ethanol appears to act directly on membrane lipids since experiments focused on protein properties [circular  ...[more]

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