scholarly article | Q13442814 |
P50 | author | Vladimir Parpura | Q48808732 |
Edwin Chapman | Q59541853 | ||
P2093 | author name string | W Liu | |
Vladimir Parpura | |||
Jihong Bai | |||
Vedrana Montana | |||
U Mohideen | |||
P2860 | cites work | Binding of the synaptic vesicle v-SNARE, synaptotagmin, to the plasma membrane t-SNARE, SNAP-25, can explain docked vesicles at neurotoxin-treated synapses | Q24671842 |
Synaptic vesicle membrane fusion complex: action of clostridial neurotoxins on assembly | Q26269962 | ||
Interactions within the yeast t-SNARE Sso1p that control SNARE complex assembly | Q27627311 | ||
Crystal structure of a SNARE complex involved in synaptic exocytosis at 2.4 A resolution | Q27765619 | ||
Homologs of the synaptobrevin/VAMP family of synaptic vesicle proteins function on the late secretory pathway in S. cerevisiae. | Q27936151 | ||
SNAP receptors implicated in vesicle targeting and fusion | Q28131653 | ||
A stable interaction between syntaxin 1a and synaptobrevin 2 mediated by their transmembrane domains | Q28140142 | ||
Mixed and non-cognate SNARE complexes. Characterization of assembly and biophysical properties | Q28144385 | ||
SNARE function analyzed in synaptobrevin/VAMP knockout mice | Q28203549 | ||
A post-docking role for synaptobrevin in synaptic vesicle fusion | Q28243803 | ||
Entropic elasticity of lambda-phage DNA | Q28247727 | ||
Protein-protein interactions contributing to the specificity of intracellular vesicular trafficking | Q28249692 | ||
Structure and conformational changes in NSF and its membrane receptor complexes visualized by quick-freeze/deep-etch electron microscopy | Q28581498 | ||
Structural organization of the synaptic exocytosis core complex | Q46275944 | ||
Synaptic transmission deficits in Caenorhabditis elegans synaptobrevin mutants. | Q47069532 | ||
Fusion pore dynamics are regulated by synaptotagmin*t-SNARE interactions. | Q47874870 | ||
Tetanus and botulinum neurotoxins are zinc proteases specific for components of the neuroexocytosis apparatus | Q48157782 | ||
Botulinum neurotoxin serotype F is a zinc endopeptidase specific for VAMP/synaptobrevin | Q48268335 | ||
A marker of early amacrine cell development in rat retina | Q48483977 | ||
Capacitance steps and fusion pores of small and large-dense-core vesicles in nerve terminals | Q48560522 | ||
Targeted expression of tetanus toxin light chain in Drosophila specifically eliminates synaptic transmission and causes behavioral defects. | Q52210225 | ||
Expression of synaptobrevin II, cellubrevin and syntaxin but not SNAP-25 in cultured astrocytes | Q57979052 | ||
Real-time measurement of transmitter release from single synaptic vesicles | Q57979058 | ||
Vesicular restriction of synaptobrevin suggests a role for calcium in membrane fusion | Q58979943 | ||
SNAP-25 and Synaptotagmin 1 Function in Ca2+-Dependent Reversible Docking of Granules to the Plasma Membrane | Q60183607 | ||
Stable SNARE complex prior to evoked synaptic vesicle fusion revealed by fluorescence resonance energy transfer | Q64380360 | ||
Insulin-induced rapid decrease of a major protein in fat cell plasma membranes | Q70498235 | ||
Kinetics of synaptotagmin responses to Ca2+ and assembly with the core SNARE complex onto membranes | Q73203897 | ||
Transport, capture and exocytosis of single synaptic vesicles at active zones | Q74265534 | ||
Genetic ablation of the t-SNARE SNAP-25 distinguishes mechanisms of neuroexocytosis | Q28591459 | ||
Tetanus toxin is a zinc protein and its inhibition of neurotransmitter release and protease activity depend on zinc | Q28609178 | ||
Membrane fusion machinery: insights from synaptic proteins | Q28609209 | ||
Tetanus and botulinum-B neurotoxins block neurotransmitter release by proteolytic cleavage of synaptobrevin | Q29619130 | ||
Single molecule observation of liposome-bilayer fusion thermally induced by soluble N-ethyl maleimide sensitive-factor attachment protein receptors (SNAREs) | Q30476464 | ||
SNARE-driven, 25-millisecond vesicle fusion in vitro | Q30476779 | ||
Botulinum toxin type B micromechanosensor | Q30501213 | ||
Stepwise unfolding of titin under force-clamp atomic force microscopy. | Q30658423 | ||
How Strong Is the Coordination Bond between a Histidine Tag and Ni - Nitrilotriacetate? An Experiment of Mechanochemistry on Single Molecules | Q30834927 | ||
Interactions between synaptic vesicle fusion proteins explored by atomic force microscopy | Q30960921 | ||
Single-molecule studies of SNARE complex assembly reveal parallel and antiparallel configurations | Q31031114 | ||
Dynamic strength of molecular adhesion bonds | Q33915225 | ||
The t-SNARE syntaxin is sufficient for spontaneous fusion of synaptic vesicles to planar membranes | Q33924441 | ||
How does calcium trigger neurotransmitter release? | Q33950706 | ||
Members of the synaptobrevin/vesicle-associated membrane protein (VAMP) family in Drosophila are functionally interchangeable in vivo for neurotransmitter release and cell viability | Q34161948 | ||
Strength of a weak bond connecting flexible polymer chains | Q34170403 | ||
Electrostatic interactions between the syntaxin membrane anchor and neurotransmitter passing through the fusion pore | Q34189535 | ||
Evidence for recycling of synaptic vesicle membrane during transmitter release at the frog neuromuscular junction | Q34207383 | ||
Probing the relation between force--lifetime--and chemistry in single molecular bonds | Q34243206 | ||
Botulinum neurotoxins are zinc proteins | Q34260095 | ||
Measurements of vesicle recycling in central neurons | Q34272558 | ||
Transmembrane segments of syntaxin line the fusion pore of Ca2+-triggered exocytosis. | Q34305380 | ||
Identifying kinetic barriers to mechanical unfolding of the T. thermophila ribozyme | Q34775534 | ||
Mechanisms of glutamate release from astrocytes: gap junction "hemichannels", purinergic receptors and exocytotic release. | Q35774444 | ||
Disruption of syntaxin-mediated protein interactions blocks neurotransmitter secretion | Q36641718 | ||
Direct measurement of the forces between complementary strands of DNA. | Q36728149 | ||
Adhesion forces between individual ligand-receptor pairs | Q36746851 | ||
Determinants of liposome fusion mediated by synaptic SNARE proteins | Q36852539 | ||
Unbinding forces of single antibody-antigen complexes correlate with their thermal dissociation rates | Q37392835 | ||
Molecular mechanisms of clostridial neurotoxins | Q40642444 | ||
Synaptobrevin binding to synaptophysin: a potential mechanism for controlling the exocytotic fusion machine. | Q40805470 | ||
Syntaxin and synaptobrevin function downstream of vesicle docking in Drosophila | Q41666993 | ||
Distinct requirements for evoked and spontaneous release of neurotransmitter are revealed by mutations in the Drosophila gene neuronal-synaptobrevin. | Q41712786 | ||
Vesicular glutamate transporter-dependent glutamate release from astrocytes. | Q44804042 | ||
Subunit interface residues of glutathione S-transferase A1-1 that are important in the monomer-dimer equilibrium | Q44808493 | ||
Reconstitution of Ca2+-regulated membrane fusion by synaptotagmin and SNAREs. | Q44814891 | ||
Syntaxin 1A drives fusion of large dense-core neurosecretory granules into a planar lipid bilayer | Q45061933 | ||
A functional role for GTP-binding proteins in synaptic vesicle cycling. | Q45988564 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P1104 | number of pages | 15 | |
P304 | page(s) | 744-758 | |
P577 | publication date | 2006-04-28 | |
P1433 | published in | Biophysical Journal | Q2032955 |
P1476 | title | Single molecule mechanical probing of the SNARE protein interactions | |
P478 | volume | 91 |