Dynamic nanoscale architecture of synaptic vesicle fusion in mouse hippocampal neurons

Synaptic vesicle (SV) fusion is not only tightly coordinated but also happens at a millisecond timescale. Competing models for fusion initiation and propagation suggest tight docking and hemifusion of SVs or localized lipid rearrangements leading to tip-like membrane contacts. Yet, a direct nanoscale examination of the full SV fusion sequence has been lacking. Here, we establish a workflow for timed in situ cryo-electron tomography of optogenetically stimulated mouse neurons to capture the complete SV fusion sequence - from SV recruitment to fusion pore formation, opening and collapse - with near-native structural preservation. Notably, tethered SVs directly undergo fusion initiation via stalk formation, without preceding tight docking or SV flattening. The plasma membrane forms a minimal dimple during fusion initiation, contradicting preceding models that invoke strong membrane bending prior to fusion. In addition, we observe filaments linking fusing SVs to adjacent SVs, indicating a physical link between fusion and SV resupply.

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Publication Details

Journal
Nature Communications
Published
2025-12-13
DOI
https://doi.org/10.1038/s41467-025-67291-6
Primary Topic
Cellular transport and secretion
Type
article
Field-Weighted Citation Impact
0.00

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article

Dynamic nanoscale architecture of synaptic vesicle fusion in mouse hippocampal neurons

Małgorzata Lubas, Christoph A. Diebolder, Mohsen Sadeghi, Mikhail Kudryashev et al.
Nature Communications
Cellular transport and secretion
article

Dynamic nanoscale architecture of synaptic vesicle fusion in mouse hippocampal neurons

Małgorzata Lubas, Christoph A. Diebolder, Mohsen Sadeghi, Mikhail Kudryashev, Magdalena Schacherl, Thiemo Sprink, Christian Rosenmund, Uljana Kravčenko, Lia Ivanov, Jana Kroll
article en

Abstract

Synaptic vesicle (SV) fusion is not only tightly coordinated but also happens at a millisecond timescale. Competing models for fusion initiation and propagation suggest tight docking and hemifusion of SVs or localized lipid rearrangements leading to tip-like membrane contacts. Yet, a direct nanoscale examination of the full SV fusion sequence has been lacking. Here, we establish a workflow for timed in situ cryo-electron tomography of optogenetically stimulated mouse neurons to capture the complete SV fusion sequence - from SV recruitment to fusion pore formation, opening and collapse - with near-native structural preservation. Notably, tethered SVs directly undergo fusion initiation via stalk formation, without preceding tight docking or SV flattening. The plasma membrane forms a minimal dimple during fusion initiation, contradicting preceding models that invoke strong membrane bending prior to fusion. In addition, we observe filaments linking fusing SVs to adjacent SVs, indicating a physical link between fusion and SV resupply.

Nature CommunicationsVol. 16(1)
Max Delbrück Center (DE), Humboldt-Universität zu Berlin (DE), Leibniz-Forschungsinstitut für Molekulare Pharmakologie (DE), Freie Universität Berlin (DE), Charité - Universitätsmedizin Berlin (DE)
Verband der Chemischen Industrie, Australasian College for Emergency Medicine, Fonds der Chemischen Industrie, Deutsche Forschungsgemeinschaft, Berlin University Alliance
Openalex Percentile: Top 58%
Cellular transport and secretion
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