4.8 Article

Tracking SNARE complex formation in live endocrine cells

Journal

SCIENCE
Volume 306, Issue 5698, Pages 1042-1046

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1102559

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Funding

  1. NIMH NIH HHS [MH60600] Funding Source: Medline

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Syntaxin, synaptosome-associated protein of 25 kD (SNAP25), and vesicle-associated membrane protein/synaptobrevin are collectively called SNAP receptor (SNARE) proteins, and they catalyze neuronal exocytosis by forming a core complex. The steps in core complex formation are unknown. Here, we monitored SNARE complex formation in vivo with the use of a fluorescent version of SNAP25. In PC12 cells, we found evidence for a syntaxin-SNAP25 complex that formed with high affinity, required only the amino-terminal SNARE motif of SNAP25, tolerated a mutation that blocks formation of other syntaxin-SNAP25 complexes, and assembled reversibly when Ca2+ entered cells during depolarization. The complex may represent a precursor to the core complex formed during a Ca2+-dependent priming step of exocytosis.

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