Munc18-1 is crucial to overcome the inhibition of synaptic vesicle fusion by αSNAP

• Published in: Nature communications Vol. 10; no. 1; pp. 4326 - 18
• Main Authors: Stepien, Karolina P., Prinslow, Eric A., Rizo, Josep
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 23-09-2019; Nature Publishing Group; Nature Portfolio
• Subjects: 101/6; 631/378/548; 631/57/1481; Animals; Binding; Cattle; Complex formation; Cricetulus; Escherichia coli - genetics; Exocytosis; Fluorescence resonance energy transfer; Humanities and Social Sciences; Magnetic resonance spectroscopy; Membrane Fusion; Membranes; multidisciplinary; Munc18 Proteins - chemistry; Munc18 Proteins - metabolism; Munc18 Proteins - physiology; Neurotransmitter release; Neurotransmitters; NMR; NMR spectroscopy; Nuclear magnetic resonance; Plasma; Protein Conformation; Rats; Science; Science (multidisciplinary); SNAP receptors; SNAP-25 protein; SNARE Proteins - metabolism; SNARE Proteins - physiology; Soluble N-Ethylmaleimide-Sensitive Factor Attachment Proteins - genetics; Soluble N-Ethylmaleimide-Sensitive Factor Attachment Proteins - metabolism; Soluble N-Ethylmaleimide-Sensitive Factor Attachment Proteins - physiology; Synaptic Vesicles - metabolism; Synaptobrevin; Syntaxin; Syntaxin 1; Syntaxin 1 - chemistry; Syntaxin 1 - metabolism; Vesicle fusion; Yeast
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-019-12188-4

Munc18-1 and Munc13-1 orchestrate assembly of the SNARE complex formed by syntaxin-1, SNAP-25 and synaptobrevin, allowing exquisite regulation of neurotransmitter release. Non-regulated neurotransmitter release might be prevented by αSNAP, which inhibits exocytosis and SNARE-dependent liposome fusion. However, distinct mechanisms of inhibition by αSNAP were suggested, and it is unknown how such inhibition is overcome. Using liposome fusion assays, FRET and NMR spectroscopy, here we provide a comprehensive view of the mechanisms underlying the inhibitory functions of αSNAP, showing that αSNAP potently inhibits liposome fusion by: binding to syntaxin-1, hindering Munc18-1 binding; binding to syntaxin-1-SNAP-25 heterodimers, precluding SNARE complex formation; and binding to trans-SNARE complexes, preventing fusion. Importantly, inhibition by αSNAP is avoided only when Munc18-1 binds first to syntaxin-1, leading to Munc18-1-Munc13-1-dependent liposome fusion. We propose that at least some of the inhibitory activities of αSNAP ensure that neurotransmitter release occurs through the highly-regulated Munc18-1-Munc13-1 pathway at the active zone.
Munc18-1 and Munc13-1 are key for the exquisite regulation of neurotransmitter release. Here biophysical experiments show how αSNAP inhibits liposome fusion mediated by the neuronal SNAREs and how Munc18-1 overcomes this inhibition, ensuring that release depends on Munc18-1 and Munc13-1.