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Munc-18
Munc-18 (an acronym for mammalian uncoordinated-18) proteins are the mammalian homologue of unc-18 proteins (which can be found in organisms such as the C. elegans) and are a member of the Sec1/Munc18-like (SM) protein family. Munc-18 proteins have been identified as essential components of the synaptic vesicle fusion protein complex and are crucial for the regulated exocytosis of neurons and neuroendocrine cells.
==Function==
Munc-18 binds syntaxin and forms a syntaxin/munc-18 complex which is thought to precede and/or regulate the formation of vesicle priming, a process mediated by VAMP, SNAP-25 and syntaxin. Munc18-1, a member of the SM family, has multiple roles in exocytosis. It directly promotes syntaxin stability and either controls the spatially correct assembly of core complexes for SNARE-dependent fusion, or acts as a direct component of the fusion machinery through the interaction with SNARE core. Munc18a, which binds specifically to the N-terminal of syntaxin, causes a conformation change, activating syntaxin, which in turn connects to the ternary-SNARE complex. Deletion of munc18-1 leads to a defect in secretory vesicle docking. Furthermore, the munc18-1 deficient mouse is the first mouse model wherein neurotransmitter secretion is completely absent. This mouse model is appropriately titled the "silent mouse."〔http://www.eni-net.org/organization/members/prof-matthijs-verhage/〕
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