A lipid-anchored SNARE supports membrane fusion

scientific article

A lipid-anchored SNARE supports membrane fusion is …
instance of (P31):
scholarly articleQ13442814

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P819ADS bibcode2011PNAS..10817325X
P356DOI10.1073/PNAS.1113888108
P932PMC publication ID3198343
P698PubMed publication ID21987819
P5875ResearchGate publication ID51708200

P50authorYoungsoo JunQ56989085
Hao XuQ56989070
P2093author name stringWilliam T Wickner
Michael Zick
P2860cites workYkt6p, a Prenylated SNARE Essential for Endoplasmic Reticulum-Golgi TransportQ24315775
Distinct SNARE complexes mediating membrane fusion in Golgi transport based on combinatorial specificityQ24534126
Membrane fusion: grappling with SNARE and SM proteinsQ24633113
The length of the flexible SNAREpin juxtamembrane region is a critical determinant of SNARE-dependent fusionQ73075597
The transmembrane domain of Vam3 affects the composition of cis- and trans-SNARE complexes to promote homotypic vacuole fusionQ78504151
Conserved structural features of the synaptic fusion complex: SNARE proteins reclassified as Q- and R-SNAREsQ24656954
Vam3p structure reveals conserved and divergent properties of syntaxinsQ27630141
Helical extension of the neuronal SNARE complex into the membraneQ27646399
Reconstituted membrane fusion requires regulatory lipids, SNAREs and synergistic SNARE chaperonesQ27931637
HOPS prevents the disassembly of trans-SNARE complexes by Sec17p/Sec18p during membrane fusionQ27932357
HOPS proofreads the trans-SNARE complex for yeast vacuole fusionQ27934773
The SNARE Ykt6 is released from yeast vacuoles during an early stage of fusionQ27934973
Purification of active HOPS complex reveals its affinities for phosphoinositides and the SNARE Vam7pQ27935373
Compartmental specificity of cellular membrane fusion encoded in SNARE proteinsQ27935841
Self-interaction of a SNARE transmembrane domain promotes the hemifusion-to-fusion transitionQ27936090
A Ypt/Rab effector complex containing the Sec1 homolog Vps33p is required for homotypic vacuole fusionQ27939110
Hemifusion in SNARE-mediated membrane fusionQ27939669
SNAREpins: minimal machinery for membrane fusionQ28131697
Structure and conformational changes in NSF and its membrane receptor complexes visualized by quick-freeze/deep-etch electron microscopyQ28581498
SNAREs--engines for membrane fusionQ29547230
Overcoming expression and purification problems of RhoGDI using a family of "parallel" expression vectorsQ29617999
Geranylgeranylated SNAREs are dominant inhibitors of membrane fusionQ30442013
HOPS initiates vacuole docking by tethering membranes before trans-SNARE complex assemblyQ33948566
Yeast vacuoles and membrane fusion pathwaysQ34086175
Use of resonance energy transfer to monitor membrane fusionQ34283693
Phosphoinositides Function Asymmetrically for Membrane Fusion, Promoting Tethering and 3Q-SNARE Subcomplex AssemblyQ34386086
Membrane fusion catalyzed by a Rab, SNAREs, and SNARE chaperones is accompanied by enhanced permeability to small molecules and by lysisQ35579819
Excess vacuolar SNAREs drive lysis and Rab bypass fusionQ35962879
Sec18p and Vam7p remodel trans-SNARE complexes to permit a lipid-anchored R-SNARE to support yeast vacuole fusionQ36274711
Interdependent assembly of specific regulatory lipids and membrane fusion proteins into the vertex ring domain of docked vacuolesQ36322803
Close is not enough: SNARE-dependent membrane fusion requires an active mechanism that transduces force to membrane anchorsQ36342484
Unraveling the mechanisms of synaptotagmin and SNARE function in neurotransmitter releaseQ36477678
Regulation of SNARE-mediated membrane fusion during exocytosisQ37140912
Capture and release of partially zipped trans-SNARE complexes on intact organellesQ37237653
Membrane fusion: SNAREs and regulationQ37251858
A soluble SNARE drives rapid docking, bypassing ATP and Sec17/18p for vacuole fusion.Q37491866
Membrane fusion: five lipids, four SNAREs, three chaperones, two nucleotides, and a Rab, all dancing in a ring on yeast vacuolesQ37762546
Neuronal SNAREs do not trigger fusion between synthetic membranes but do promote PEG-mediated membrane fusionQ42077784
HOPS drives vacuole fusion by binding the vacuolar SNARE complex and the Vam7 PX domain via two distinct sitesQ42801354
P433issue42
P407language of work or nameEnglishQ1860
P304page(s)17325-17330
P577publication date2011-10-10
P1433published inProceedings of the National Academy of Sciences of the United States of AmericaQ1146531
P1476titleA lipid-anchored SNARE supports membrane fusion
P478volume108

Reverse relations

cites work (P2860)
Q41808432A Central Small Amino Acid in the VAMP2 Transmembrane Domain Regulates the Fusion Pore in Exocytosis.
Q57973663A novel in vitro assay reveals SNARE topology and the role of Ykt6 in autophagosome fusion with vacuoles
Q49911437Dynamic Cycling of t-SNARE Acylation Regulates Platelet Exocytosis
Q37719014Familial hemophagocytic lymphohistiocytosis: when rare diseases shed light on immune system functioning
Q57454590Functional Reconstitution of Intracellular Vesicle Fusion Using Purified SNAREs and Sec1/Munc18 (SM) Proteins
Q39123295Fusion pores and their control of neurotransmitter and hormone release.
Q37703099Hemifusion in Synaptic Vesicle Cycle.
Q37023429Individual vesicle fusion events mediated by lipid-anchored DNA.
Q28079024Invited review: Mechanisms of GTP hydrolysis and conformational transitions in the dynamin superfamily
Q28384856Lipid Geometry and Bilayer Curvature Modulate LC3/GABARAP-Mediated Model Autophagosomal Elongation
Q26269847Lipid-anchored SNAREs lacking transmembrane regions fully support membrane fusion during neurotransmitter release
Q36548383Lipid-anchored Synaptobrevin Provides Little or No Support for Exocytosis or Liposome Fusion.
Q57173506Mechanism of neurotransmitter release coming into focus
Q30414376Membranes linked by trans-SNARE complexes require lipids prone to non-bilayer structure for progression to fusion
Q34277591Mitofusins and the mitochondrial permeability transition: the potential downside of mitochondrial fusion
Q35451364Munc18a does not alter fusion rates mediated by neuronal SNAREs, synaptotagmin, and complexin
Q42142889Phosphatidylserine-Dependent Catalysis of Stalk and Pore Formation by Synaptobrevin JMR-TMD Peptide.
Q35055470Rho GTPases and the downstream effectors actin-related protein 2/3 (Arp2/3) complex and myosin II induce membrane fusion at self-contacts.
Q38926137SM protein Munc18-2 facilitates transition of Syntaxin 11-mediated lipid mixing to complete fusion for T-lymphocyte cytotoxicity
Q41215060Sec17/Sec18 act twice, enhancing membrane fusion and then disassembling cis-SNARE complexes.
Q40627999Synaptobrevin Transmembrane Domain Dimerization Studied by Multiscale Molecular Dynamics Simulations
Q39121037The Multifaceted Role of SNARE Proteins in Membrane Fusion.
Q57056881The N-peptide binding mode is critical to Munc18-1 function in synaptic exocytosis
Q90253180The Transmembrane Domain of Synaptobrevin Influences Neurotransmitter Flux through Synaptic Fusion Pores
Q36344941The trans-SNARE-regulating function of Munc18-1 is essential to synaptic exocytosis
Q35608147Vacuolar SNARE protein transmembrane domains serve as nonspecific membrane anchors with unequal roles in lipid mixing