Munc-18 (an acronym for mammalian uncoordinated-18) proteins are the mammalian homologue of UNC-18 (which was first discovered in the nematode worm C. elegans[1][2]) 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.[3]
Function[edit]
Munc-18 binds syntaxin and forms a syntaxin/munc-18 complex which is thought to precede and/or regulate vesicle priming, a process mediated by VAMP, SNAP-25 and syntaxin.[4] Munc18-1, a member of the SM family, has multiple roles in exocytosis.[5] 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.[6] 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.[7] Deletion of munc18-1 leads to a defect in secretory vesicle docking.[8] 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."[9]
Mechanism[edit]
This outline below presents a broad modeling of how Munc-18 is thought to play a role in vesicle docking and fusion, allowing for intentional exocytosis.[10] As it is a combined preliminary modeling, more research is necessary to fully understand the role of Munc-18 in this process.
- Munc18-1 binds to a closed form of syntaxin-1, blocking SNARE complex formation. This is thought to affect vesicle docking
- Munc13 opens syntaxin-1, Munc18-1 is translocated to the SNARE complex, which releases the inhibitory effect, allowing assembly (specifically of the alpha helix 4 part bundle)
- It is thought that Munc18-1 stabilizes the formed trans-SNARE complex, preventing its dissociation
- The SNARE complex, potentially with the assistance of Munc-18 brings the membranes together and causes fusion
It has also been shown in one study that Munc-18 binds to the C-terminus of synaptobrevin, suggesting that this protein plays an important role in membrane fusion.[11]
Family members[edit]
The following is a list of human munc-18 proteins:
| protein | gene | |
|---|---|---|
| symbol | name | |
| MUNC18-1 | STXBP1 | syntaxin binding protein 1 |
| MUNC18-2 | STXBP2 | syntaxin binding protein 2 |
| MUNC18-3 | STXBP3 | syntaxin binding protein 3 |
| MUNC18-4 | STXBP4 | syntaxin binding protein 4 |
| MUNC18-5 | STXBP5 | syntaxin binding protein 5 |
| MUNC18-6 | STXBP6 | syntaxin binding protein 6 |
See also[edit]
References[edit]
- ^ Hosono R (1992). "The unc-18 Gene Encodes a Novel Protein Affecting the Kinetics of Acetylcholine Metabolism in the Nematode Caenorhabditis elegans". Journal of Neurochemistry. 58 (4): 1517–1525. doi:10.1111/j.1471-4159.1992.tb11373.x. PMID 1347782. S2CID 30965606.
- ^ Brenner, S. (May 1974). "The Genetics of Caenorhabditis Elegans". Genetics. 77 (1): 71–94. doi:10.1093/genetics/77.1.71. PMC 1213120. PMID 4366476.
- ^ Zilly FE, Sørensen JB, Jahn R, Lang T (October 2006). "Munc18-bound syntaxin readily forms SNARE complexes with synaptobrevin in native plasma membranes". PLOS Biol. 4 (10): e330. doi:10.1371/journal.pbio.0040330. PMC 1570500. PMID 17002520.
- ^ Pevsner J, Hsu SC, Braun JE, Calakos N, Ting AE, Bennett MK, Scheller RH (August 1994). "Specificity and regulation of a synaptic vesicle docking complex". Neuron. 13 (2): 353–61. doi:10.1016/0896-6273(94)90352-2. PMID 8060616. S2CID 46713725.
- ^ Burgoyne RD, Barclay JW, Ciufo LF, Graham ME, Handley MT, Morgan A (2009). "The functions of Munc18-1 in regulated exocytosis". Ann N Y Acad Sci. 1152 (1): 76–86. Bibcode:2009NYASA1152...76B. doi:10.1111/j.1749-6632.2008.03987.x. PMID 19161378. S2CID 30026611.
- ^ Diao J, Su Z, Lu X, Yoon TY, Shin YK, Ha T (March 2010). "Single-Vesicle Fusion Assay Reveals Munc18-1 Binding to the SNARE Core Is Sufficient for Stimulating Membrane Fusion". ACS Chem Neurosci. 1 (3): 168–174. doi:10.1021/cn900034p. PMC 2841011. PMID 20300453.
- ^ Kasai, H.; Takahashi, N.; Tokumaru, H. (2012). "Distinct Initial SNARE Configurations Underlying the Diversity of Exocytosis". Physiological Reviews. 92 (4): 1915–1964. doi:10.1152/physrev.00007.2012. PMID 23073634.
- ^ Toonen RF, de Vries KJ, Zalm R, Südhof TC, Verhage M (June 2005). "Munc18-1 stabilizes syntaxin 1, but is not essential for syntaxin 1 targeting and SNARE complex formation". J. Neurochem. 93 (6): 1393–400. doi:10.1111/j.1471-4159.2005.03128.x. PMID 15935055. S2CID 24920185.
- ^ "Members :: Network of European Neuroscience Institutes". Archived from the original on 2009-08-18. Retrieved 2010-02-05.
- ^ Rizo, J.; Südhof, T. C. (2012). "The Membrane Fusion Enigma: SNAREs, Sec1/Munc18 Proteins, and Their Accomplices—Guilty as Charged?". Annual Review of Cell and Developmental Biology. 28: 279–308. doi:10.1146/annurev-cellbio-101011-155818. PMID 23057743.
- ^ Xu, Y; Su, L; Rizo, J (2 March 2010). "Binding of Munc18-1 to synaptobrevin and to the SNARE four-helix bundle". Biochemistry. 49 (8): 1568–76. doi:10.1021/bi9021878. PMC 2834481. PMID 20102228.
External links[edit]
- Munc18+Proteins at the U.S. National Library of Medicine Medical Subject Headings (MeSH)