Structural and Functional Analysis of the CAPS SNARE-Binding Domain Required for SNARE Complex Formation and Exocytosis.

Summary Exocytosis of synaptic vesicles and dense-core vesicles requires both the Munc13 and CAPS (Ca²⁺-dependent activator proteins for secretion) proteins. CAPS contains a soluble N -ethylmaleimide-sensitive factor attachment protein receptor (SNARE)-binding region (called the DAMH domain), which has been found to be essential for SNARE-mediated exocytosis. Here we report a crystal structure of the CAPS-1 DAMH domain at 2.9-Å resolution and reveal a dual role of CAPS-1 in SNARE complex formation. CAPS-1 plays an inhibitory role dependent on binding of the DAMH domain to the MUN domain of Munc13-1, which hinders the ability of Munc13 to catalyze opening of syntaxin-1, inhibiting SNARE complex formation, and a chaperone role dependent on interaction of the DAMH domain with the syntaxin-1/SNAP-25 complex, which stabilizes the open conformation of Syx1, facilitating SNARE complex formation. Our results suggest that CAPS-1 facilitates SNARE complex formation via the DAMH domain in a manner dependent on sequential and cooperative interaction with Munc13-1 and SNARE proteins. Graphical Abstract Highlights • A structure of the DAMH domain of CAPS is presented • CAPS hinders the ability of Munc13to catalyze opening of syntaxin-1 • CAPS stabilizes the open state of syntaxin-1 to facilitate SNARE complex formation CAPS and Munc13, as major priming factors for exocytosis, play an important role in SNARE-mediated membrane fusion. Zhou et al. present the crystal structure of the DAMH domain of CAPS and reveal a molecular link between the roles of CAPS and Munc13 in SNARE complex formation. [ABSTRACT FROM AUTHOR]