Phosphatidylinositol 4,5-bisphosphate clusters act as molecular beacons for vesicle recruitment.

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2013

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info:eu-repo/semantics/altIdentifier/doi/10.1038/nsmb.2570

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info:eu-repo/semantics/altIdentifier/pmid/23665582

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info:eu-repo/semantics/altIdentifier/eissn/1545-9985

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info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_2132D45084C02

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Fusion, Membrane

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A. Honigmann et al., « Phosphatidylinositol 4,5-bisphosphate clusters act as molecular beacons for vesicle recruitment. », Serveur académique Lausannois, ID : 10.1038/nsmb.2570


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Synaptic-vesicle exocytosis is mediated by the vesicular Ca(2+) sensor synaptotagmin-1. Synaptotagmin-1 interacts with the SNARE protein syntaxin-1A and acidic phospholipids such as phosphatidylinositol 4,5-bisphosphate (PIP2). However, it is unclear how these interactions contribute to triggering membrane fusion. Using PC12 cells from Rattus norvegicus and artificial supported bilayers, we show that synaptotagmin-1 interacts with the polybasic linker region of syntaxin-1A independent of Ca(2+) through PIP2. This interaction allows both Ca(2+)-binding sites of synaptotagmin-1 to bind to phosphatidylserine in the vesicle membrane upon Ca(2+) triggering. We determined the crystal structure of the C2B domain of synaptotagmin-1 bound to phosphoserine, allowing development of a high-resolution model of synaptotagmin bridging two different membranes. Our results suggest that PIP2 clusters organized by syntaxin-1 act as molecular beacons for vesicle docking, with the subsequent Ca(2+) influx bringing the vesicle membrane close enough for membrane fusion.

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