Journal
DEVELOPMENTAL CELL
Volume 12, Issue 4, Pages 653-659Publisher
CELL PRESS
DOI: 10.1016/j.devcel.2007.02.007
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Funding
- NICHD NIH HHS [R01 HD028152] Funding Source: Medline
- NIGMS NIH HHS [T32 GM007601] Funding Source: Medline
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Membrane fusion during exocytosis requires that two initially distinct bilayers; pass through a hemifused intermediate in which the proximal monolayers are shared. Passage through this intermediate is an essential step in the process of secretion, but is difficult to observe directly in vivo. Here we study membrane fusion in the sea urchin egg, in which thousands of homogeneous cortical granules are associated with the plasma membrane prior to fertilization. Using fluorescence redistribution after photo-bleaching, we find that these granules are stably hemifused to the plasma membrane, sharing a cytoplasmic-facing monolayer. Furthermore, we find that the proteins implicated in the fusion process-the vesicle-associated proteins VAMP/synaptobrevin, synaptotagmin, and Rab3-are each immobile within the granule membrane. Thus, these secretory granules are tethered to their target plasma membrane by a static, catalytic fusion complex that maintains a hemifused membrane intermediate.
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