The Last Seconds in the Life of a Secretory Vesicle

  1. T.D. Parsons1,
  2. J.R. Coorssen1,
  3. H. Hortmann1,
  4. A.K. Lee2,
  5. F.W. Tse2, and
  6. W. Almers1
  1. 1Abteilung Molekulare Zellforschung, Max Planck Institut fur Medizinische Forschung, 69120 Heidelberg, Germany; 2Department of Pharmacology, University of Alberta, Edmonton, Alberta T6G 2H7, Canada

This extract was created in the absence of an abstract.

Excerpt

Regulated exocytosis may be divided into four steps: the docking of the secretory vesicle to the plasmalemma, the “priming” of the exocytotic machinery, the triggering of exocytosis by cytosolic Ca++, and, ultimately, the fusion of the vesicle membrane to the plasmalemma. As reviewed elsewhere (Ferro-Novick and Jahn 1994; Rothmann 1994; Scheller 1995; Südhof 1995), biochemical and molecular genetic studies have made significant progress in establishing the molecular basis for some of these steps. Docking has been proposed to include the binding of a “v-SNARE” (a membrane protein in the secretory vesicle, VAMP/synaptobrevin in synaptic vesicles) to two t-SNAREs in the plasmalemma (syntaxin and SNAP-25 in presynaptic terminals; Sollner et al. 1993). v- and t-SNAREs form a stable trimeric complex with a characteristic sedimentation coefficient of 7S. Priming refers to the last Mg-ATP-dependent reaction (or reactions) in the exocytotic pathway. Exocytosis universally requires Mg-ATP, but in neuroendocrine cells, ATP hydrolysis does...

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