Molecular Biology of the Cell · 2000 · 163 citations · 50 references
Life SciencesBiochemistryCell BiologyCell SignalingEndocytosisMembrane TraffickingEndomembrane SystemEndosomal TraffickingLate EndosomesSnare-mediated FusionVesicle FusionVesicle TraffickingAntibodiesEndosome FusionFractionationFusion ReactionsMembrane Snare ComplexesSnare ProteinsSubcellular FractionationVamp8 Function
Endobrevin/VAMP-8 is an R-SNARE localized to endosomes, but it is unknown in which intracellular fusion step it operates. Using subcellular fractionation and quantitative immunogold electron microscopy, we found that endobrevin/VAMP-8 is present on all membranes known to communicate with early endosomes, including the plasma membrane, clathrin-coated pits, late endosomes, and membranes of the trans-Golgi network. Affinity-purified antibodies that block the ability of endobrevin/VAMP-8 to form SNARE core complexes potently inhibit homotypic fusion of both early and late endosomes in vitro. Fab fragments were as active as intact immunoglobulin Gs. Recombinant endobrevin/VAMP-8 inhibited both fusion reactions with similar potency. We conclude that endobrevin/VAMP-8 operates as an R-SNARE in the homotypic fusion of early and late endosomes.
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SNAP receptors implicated in vesicle targeting and fusion
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Crystal structure of a SNARE complex involved in synaptic exocytosis at 2.4 Å resolution
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