<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Park Y</submitter><funding>NIGMS NIH HHS</funding><pagination>991-7</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3465474</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(10)</volume><pubmed_abstract>Exocytosis of neurosecretory vesicles is mediated by the SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein receptor) proteins syntaxin-1, synaptobrevin and SNAP-25, with synaptotagmin functioning as the major Ca(2+) sensor for triggering membrane fusion. Here we show that bovine chromaffin granules readily fuse with large unilamellar liposomes in a SNARE-dependent manner. Fusion is enhanced by Ca(2+), but only when the target liposomes contain phosphatidylinositol-4,5-bisphosphate and when polyphosphate anions, such as nucleotides or pyrophosphate, are present. Ca(2+)-dependent enhancement is mediated by endogenous synaptotagmin-1. Polyphosphates operate by an electrostatic mechanism that reverses an inactivating cis association of synaptotagmin-1 with its own membrane without affecting trans binding. Hence, the balancing of trans- and cis-membrane interactions of synaptotagmin-1 could be a crucial element in the pathway of Ca(2+)-dependent exocytosis.</pubmed_abstract><journal>Nature structural &amp; molecular biology</journal><pubmed_title>Controlling synaptotagmin activity by electrostatic screening.</pubmed_title><pmcid>PMC3465474</pmcid><funding_grant_id>P01 GM072694</funding_grant_id><funding_grant_id>2 P01 GM072694-06A1</funding_grant_id><pubmed_authors>Jahn R</pubmed_authors><pubmed_authors>Park Y</pubmed_authors><pubmed_authors>Ahmed S</pubmed_authors><pubmed_authors>van den Bogaart G</pubmed_authors><pubmed_authors>Holt M</pubmed_authors><pubmed_authors>Hernandez JM</pubmed_authors><pubmed_authors>Riedel D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Controlling synaptotagmin activity by electrostatic screening.</name><description>Exocytosis of neurosecretory vesicles is mediated by the SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein receptor) proteins syntaxin-1, synaptobrevin and SNAP-25, with synaptotagmin functioning as the major Ca(2+) sensor for triggering membrane fusion. Here we show that bovine chromaffin granules readily fuse with large unilamellar liposomes in a SNARE-dependent manner. Fusion is enhanced by Ca(2+), but only when the target liposomes contain phosphatidylinositol-4,5-bisphosphate and when polyphosphate anions, such as nucleotides or pyrophosphate, are present. Ca(2+)-dependent enhancement is mediated by endogenous synaptotagmin-1. Polyphosphates operate by an electrostatic mechanism that reverses an inactivating cis association of synaptotagmin-1 with its own membrane without affecting trans binding. Hence, the balancing of trans- and cis-membrane interactions of synaptotagmin-1 could be a crucial element in the pathway of Ca(2+)-dependent exocytosis.</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Oct</publication><modification>2025-04-05T12:55:05.427Z</modification><creation>2019-03-27T00:58:49Z</creation></dates><accession>S-EPMC3465474</accession><cross_references><pubmed>22940675</pubmed><doi>10.1038/nsmb.2375</doi></cross_references></HashMap>