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Large α-synuclein oligomers inhibit neuronal SNARE-mediated vesicle docking
Author(s) -
BongKyu Choi,
MalGi Choi,
Jae Yeol Kim,
Yoosoo Yang,
Ying Lai,
DaeHyuk Kweon,
Nam Ki Lee,
YeonKyun Shin
Publication year - 2013
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1218424110
Subject(s) - synaptic vesicle , chemistry , alpha synuclein , biophysics , microbiology and biotechnology , vesicle , fibril , lewy body , snare complex , snap25 , synaptobrevin , neurotoxin , neurotoxicity , biochemistry , biology , parkinson's disease , membrane , toxicity , medicine , disease , pathology , organic chemistry
Parkinson disease and dementia with Lewy bodies are featured with the formation of Lewy bodies composed mostly of α-synuclein (α-Syn) in the brain. Although evidence indicates that the large oligomeric or protofibril forms of α-Syn are neurotoxic agents, the detailed mechanisms of the toxic functions of the oligomers remain unclear. Here, we show that large α-Syn oligomers efficiently inhibit neuronal SNARE-mediated vesicle lipid mixing. Large α-Syn oligomers preferentially bind to the N-terminal domain of a vesicular SNARE protein, synaptobrevin-2, which blocks SNARE-mediated lipid mixing by preventing SNARE complex formation. In sharp contrast, the α-Syn monomer has a negligible effect on lipid mixing even with a 30-fold excess compared with the case of large α-Syn oligomers. Thus, the results suggest that large α-Syn oligomers function as inhibitors of dopamine release, which thus provides a clue, at the molecular level, to their neurotoxicity.

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