Transition from hemifusion to pore opening is rate limiting for vacuole membrane fusion
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The V-ATPase proteolipid cylinder promotes the lipid-mixing stage of SNARE-dependent fusion of yeast vacuoles.Phosphatidic Acid Sequesters Sec18p from cis-SNARE Complexes to Inhibit PrimingThe Central Polybasic Region of the Soluble SNARE (Soluble N-Ethylmaleimide-sensitive Factor Attachment Protein Receptor) Vam7 Affects Binding to Phosphatidylinositol 3-Phosphate by the PX (Phox Homology) Domain.Yeast lipin 1 orthologue pah1p regulates vacuole homeostasis and membrane fusion.Reovirus FAST Proteins Drive Pore Formation and Syncytiogenesis Using a Novel Helix-Loop-Helix Fusion-Inducing Lipid Packing SensorDocking and fast fusion of synaptobrevin vesicles depends on the lipid compositions of the vesicle and the acceptor SNARE complex-containing target membrane.Multiple intermediates in SNARE-induced membrane fusion.How and why intralumenal membrane fragments form during vacuolar lysosome fusion.Atomic force microscope spectroscopy reveals a hemifusion intermediate during soluble N-ethylmaleimide-sensitive factor-attachment protein receptors-mediated membrane fusionInvestigation of SNARE-Mediated Membrane Fusion Mechanism Using Atomic Force Microscopy.The fusion pores of Ca2+ -triggered exocytosisMitofusins and the mitochondrial permeability transition: the potential downside of mitochondrial fusionAre there too many or too few SNAREs in proteoliposomes?Cell-free reconstitution of vacuole membrane fragmentation reveals regulation of vacuole size and number by TORC1.Trans-SNARE complex assembly and yeast vacuole membrane fusion.Assays of vacuole fusion resolve the stages of docking, lipid mixing, and content mixingMembranes of the world unite!Synaptic proteins promote calcium-triggered fast transition from point contact to full fusion.The conserved plant sterility gene HAP2 functions after attachment of fusogenic membranes in Chlamydomonas and Plasmodium gametesThe yeast vacuolar ABC transporter Ybt1p regulates membrane fusion through Ca2+ transport modulationThe lipid composition and physical properties of the yeast vacuole affect the hemifusion-fusion transition.Capture and release of partially zipped trans-SNARE complexes on intact organelles.The membrane domain of vacuolar H(+)ATPase: a crucial player in neurotransmitter exocytotic release.Deleting the DAG kinase Dgk1 augments yeast vacuole fusion through increased Ypt7 activity and altered membrane fluidity.Class C ABC transporters and Saccharomyces cerevisiae vacuole fusionSteric hindrance of SNARE transmembrane domain organization impairs the hemifusion-to-fusion transition.The vacuolar V1/V0-ATPase is involved in the release of the HOPS subunit Vps41 from vacuoles, vacuole fragmentation and fusion.The hallmarks of cell-cell fusion.Sequential actions of phosphatidylinositol phosphates regulate phagosome-lysosome fusion.Phospholipase D1 Production of Phosphatidic Acid at the Plasma Membrane Promotes Exocytosis of Large Dense-core Granules at a Late Stage
P2860
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P2860
Transition from hemifusion to pore opening is rate limiting for vacuole membrane fusion
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
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2005年學術文章
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2005年學術文章
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name
Transition from hemifusion to pore opening is rate limiting for vacuole membrane fusion
@ast
Transition from hemifusion to pore opening is rate limiting for vacuole membrane fusion
@en
type
label
Transition from hemifusion to pore opening is rate limiting for vacuole membrane fusion
@ast
Transition from hemifusion to pore opening is rate limiting for vacuole membrane fusion
@en
prefLabel
Transition from hemifusion to pore opening is rate limiting for vacuole membrane fusion
@ast
Transition from hemifusion to pore opening is rate limiting for vacuole membrane fusion
@en
P2860
P356
P1476
Transition from hemifusion to pore opening is rate limiting for vacuole membrane fusion
@en
P2093
Christoph Reese
P2860
P304
P356
10.1083/JCB.200510018
P407
P577
2005-12-01T00:00:00Z