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PRRT2 Regulates Synaptic Fusion by Directly Modulating SNARE Complex Assembly

Title: PRRT2 Regulates Synaptic Fusion by Directly Modulating SNARE Complex Assembly
Authors: Coleman, J; Jouannot, O; Ramakrishnan, SK; Zanetti, MN; Wang, J; Salpietro, V; Houlden, H; Rothman, JE; Krishnakumar, SS
Source: Cell Reports , 22 (3) pp. 820-831. (2018)
Publisher Information: CELL PRESS
Publication Year: 2018
Collection: University College London: UCL Discovery
Subject Terms: Science & Technology; Life Sciences & Biomedicine; Cell Biology; PAROXYSMAL KINESIGENIC DYSKINESIA; MEMBRANE-FUSION; NEUROTRANSMITTER RELEASE; SYNAPTOTAGMIN-I; VESICLE FUSION; PROTEINS; EXOCYTOSIS; MUTATIONS; DYNAMICS; PROLINE
Description: Mutations in proline-rich transmembrane protein 2 (PRRT2) are associated with a range of paroxysmal neurological disorders. PRRT2 predominantly localizes to the pre-synaptic terminals and is believed to regulate neurotransmitter release. However, the mechanism of action is unclear. Here, we use reconstituted single vesicle and bulk fusion assays, combined with live cell imaging of single exocytotic events in PC12 cells and biophysical analysis, to delineate the physiological role of PRRT2. We report that PRRT2 selectively blocks the trans SNARE complex assembly and thus negatively regulates synaptic vesicle priming. This inhibition is actualized via weak interactions of the N-terminal proline-rich domain with the synaptic SNARE proteins. Furthermore, we demonstrate that paroxysmal dyskinesia-associated mutations in PRRT2 disrupt this SNARE-modulatory function and with efficiencies corresponding to the severity of the disease phenotype. Our findings provide insights into the molecular mechanisms through which loss-of-function mutations in PRRT2 result in paroxysmal neurological disorders.
Document Type: article in journal/newspaper
File Description: text
Language: English
Relation: https://discovery.ucl.ac.uk/id/eprint/10043570/
Availability: https://discovery.ucl.ac.uk/id/eprint/10043570/1/1-s2.0-S2211124717318806-main.pdf; https://discovery.ucl.ac.uk/id/eprint/10043570/
Rights: open
Accession Number: edsbas.F062EAA9
Database: BASE