v-SNARE Actions during Ca2+-Triggered Exocytosis

Cell

Volumn 131, Issue 2, 2007, Pages 351-363

  Kesavan, Jaideep ^a   Borisovska, Maria ^a   Bruns, Dieter ^a  

^a SAARLAND UNIVERSITY   (Germany)

Author keywords

CELLBIO; MOLNEURO

Indexed keywords

CALCIUM; LIPOSOME; SNARE PROTEIN; SYNAPTOBREVIN 2;

ANIMAL CELL; ARTICLE; CALCIUM CELL LEVEL; CELL GRANULE; CHANNEL GATING; CHROMAFFIN GRANULE; EXOCYTOSIS; MEMBRANE FUSION; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN BINDING; PROTEIN DOMAIN; PROTEIN FUNCTION; SECRETORY VESICLE;

EID: 35348925451     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cell.2007.09.025     Document Type: Article

References (53)

1. Albillos A., Dernick G., Horstmann H., Almers W., Alvarez de Toledo G., and Lindau M. The exocytotic event in chromaffin cells revealed by patch amperometry. Nature 389 (1997) 509-512
2. 2+-dependent multivalent binding of synaptotagmin-1 to phospholipids. Nat. Struct. Mol. Biol. 13 (2006) 209-217
3. Ashery U., Betz A., Xu T., Brose N., and Rettig J. An efficient method for infection of adrenal chromaffin cells using the Semliki Forest virus gene expression system. Eur. J. Cell Biol. 78 (1999) 525-532
4. * t-SNARE interactions. Neuron 41 (2004) 929-942
5. 2+-synaptotagmin directly regulates t-SNARE function during reconstituted membrane fusion. Nat. Struct. Mol. Biol. 13 (2006) 323-330
6. Borisovska M., Zhao Y., Tsytsyura Y., Glyvuk N., Takamori S., Matti U., Rettig J., Sudhof T., and Bruns D. v-SNAREs control exocytosis of vesicles from priming to fusion. EMBO J. 24 (2005) 2114-2126
7. Bowen M.E., Weninger K., Brunger A.T., and Chu S. Single molecule observation of liposome-bilayer fusion thermally induced by soluble N-ethyl maleimide sensitive-factor attachment protein receptors (SNAREs). Biophys. J. 87 (2004) 3569-3584
8. Bruns D. Detection of transmitter release with carbon fiber electrodes. Methods 33 (2004) 312-321
9. Bruns D., and Jahn R. Real-time measurement of transmitter release from single synaptic vesicles. Nature 377 (1995) 62-65
10. 2+ sensor that triggers exocytosis?. Nat. Rev. Mol. Cell Biol. 3 (2002) 498-508
11. Chernomordik L.V., and Kozlov M.M. Membrane hemifusion: crossing a chasm in two leaps. Cell 123 (2005) 375-382
12. Chow R.H., von Ruden L., and Neher E. Delay in vesicle fusion revealed by electrochemical monitoring of single secretory events in adrenal chromaffin cells. Nature 356 (1992) 60-63
13. Colquhoun D., and Sigworth F.J. Fitting and Statistical analysis of Single-Channel Records. In: Sakmann B., and Neher E. (Eds). Single-Channel Recording (1995), Plenum Press, New York 483-585
14. 2+-phospholipid complex in neurotransmitter release. J. Mol. Biol. 367 (2007) 848-863
15. Deak F., Shin O.H., Kavalali E.T., and Sudhof T.C. Structural determinants of synaptobrevin 2 function in synaptic vesicle fusion. J. Neurosci. 26 (2006) 6668-6676
16. Dennison S.M., Bowen M.E., Brunger A.T., and Lentz B.R. Neuronal SNAREs do not trigger fusion between synthetic membranes but do promote PEG-mediated membrane fusion. Biophys. J. 90 (2006) 1661-1675
17. Fernandez-Chacon R., Konigstorfer A., Gerber S.H., Garcia J., Matos M.F., Stevens C.F., Brose N., Rizo J., Rosenmund C., and Sudhof T.C. Synaptotagmin I functions as a calcium regulator of release probability. Nature 410 (2001) 41-49
18. 2+ sensor for transmitter release at a central synapse. Cell 79 (1994) 717-727
19. Giraudo C.G., Eng W.S., Melia T.J., and Rothman J.E. A clamping mechanism involved in SNARE-dependent exocytosis. Science 313 (2006) 676-680
20. Giraudo C.G., Hu C., You D., Slovic A.M., Mosharov E.V., Sulzer D., Melia T.J., and Rothman J.E. SNAREs can promote complete fusion and hemifusion as alternative outcomes. J. Cell Biol. 170 (2005) 249-260
21. 2+-triggered exocytosis. J. Cell Biol. 172 (2006) 281-293
22. Hannah M.J., Weiss U., and Huttner W.B. Differential extraction of proteins from paraformaldehyde-fixed cells: lessons from synaptophysin and other membrane proteins. Methods 16 (1998) 170-181
23. Hanson P.I., Roth R., Morisaki H., Jahn R., and Heuser J.E. Structure and conformational changes in NSF and its membrane receptor complexes visualized by quick-freeze/deep-etch electron microscopy. Cell 90 (1997) 523-535
24. Higuchi R. Using PCR to Engenieer DNA (1989), Stockton Press, New York, NY
25. Hua S.Y., and Charlton M.P. Activity-dependent changes in partial VAMP complexes during neurotransmitter release. Nat. Neurosci. 2 (1999) 1078-1083
26. Jackson M.B., and Chapman E.R. Fusion pores and fusion machines in Ca2+-triggered exocytosis. Annu. Rev. Biophys. Biomol. Struct. 35 (2006) 135-160
27. Jahn R., and Scheller R.H. SNAREs-engines for membrane fusion. Nat. Rev. Mol. Cell Biol. 7 (2006) 631-643
28. Lin R.C., and Scheller R.H. Structural organization of the synaptic exocytosis core complex. Neuron 19 (1997) 1087-1094
29. Martens S., Kozlov M.M., and McMahon H.T. How synaptotagmin promotes membrane fusion. Science 316 (2007) 1205-1208
30. McNew J.A., Weber T., Engelman D.M., Sollner T.H., and Rothman J.E. The length of the flexible SNAREpin juxtamembrane region is a critical determinant of SNARE-dependent fusion. Mol. Cell 4 (1999) 415-421
31. Nagy G., Kim J.H., Pang Z.P., Matti U., Rettig J., Sudhof T.C., and Sorensen J.B. Different effects on fast exocytosis induced by synaptotagmin 1 and 2 isoforms and abundance but not by phosphorylation. J. Neurosci. 26 (2006) 632-643
32. Nickel W., Weber T., McNew J.A., Parlati F., Sollner T.H., and Rothman J.E. Content mixing and membrane integrity during membrane fusion driven by pairing of isolated v-SNAREs and t-SNAREs. Proc. Natl. Acad. Sci. USA 96 (1999) 12571-12576
33. Pobbati A.V., Stein A., and Fasshauer D. N- to C-terminal SNARE complex assembly promotes rapid membrane fusion. Science 313 (2006) 673-676
34. Reese C., Heise F., and Mayer A. Trans-SNARE pairing can precede a hemifusion intermediate in intracellular membrane fusion. Nature 436 (2005) 410-414
35. Reim K., Mansour M., Varoqueaux F., McMahon H.T., Sudhof T.C., Brose N., and Rosenmund C. Complexins regulate a late step in Ca2+-dependent neurotransmitter release. Cell 104 (2001) 71-81
36. ++-triggered exocytosis. Science 298 (2002) 781-785
37. Sakaba T., Stein A., Jahn R., and Neher E. Distinct kinetic changes in neurotransmitter release after SNARE protein cleavage. Science 309 (2005) 491-494
38. 2+-synaptotagmin I. Nat. Struct. Mol. Biol. 13 (2006) 748-750
39. 2+. J. Gen. Physiol. 122 (2003) 265-276
40. Sorensen J.B., Matti U., Wei S.H., Nehring R.B., Voets T., Ashery U., Binz T., Neher E., and Rettig J. The SNARE protein SNAP-25 is linked to fast calcium triggering of exocytosis. Proc. Natl. Acad. Sci. USA 99 (2002) 1627-1632
41. Sorensen J.B., Wiederhold K., Muller E.M., Milosevic I., Nagy G., de Groot B.L., Grubmuller H., and Fasshauer D. Sequential N- to C-terminal SNARE complex assembly drives priming and fusion of secretory vesicles. EMBO J. 25 (2006) 955-966
42. Sutton R.B., Fasshauer D., Jahn R., and Brunger A.T. Crystal structure of a SNARE complex involved in synaptic exocytosis at 2.4 A resolution. Nature 395 (1998) 347-353
43. Tang J., Maximov A., Shin O.H., Dai H., Rizo J., and Sudhof T.C. A complexin/synaptotagmin 1 switch controls fast synaptic vesicle exocytosis. Cell 126 (2006) 1175-1187
44. Voets T., Moser T., Lund P.E., Chow R.H., Geppert M., Sudhof T.C., and Neher E. Intracellular calcium dependence of large dense-core vesicle exocytosis in the absence of synaptotagmin I. Proc. Natl. Acad. Sci. USA 98 (2001) 11680-11685
45. Voets T., Neher E., and Moser T. Mechanisms underlying phasic and sustained secretion in chromaffin cells from mouse adrenal slices. Neuron 23 (1999) 607-615
46. Wang C.T., Grishanin R., Earles C.A., Chang P.Y., Martin T.F., Chapman E.R., and Jackson M.B. Synaptotagmin modulation of fusion pore kinetics in regulated exocytosis of dense-core vesicles. Science 294 (2001) 1111-1115
47. Weber T., Zemelman B.V., McNew J.A., Westermann B., Gmachl M., Parlati F., Sollner T.H., and Rothman J.E. SNAREpins: minimal machinery for membrane fusion. Cell 92 (1998) 759-772
48. Wong J.L., Koppel D.E., Cowan A.E., and Wessel G.M. Membrane hemifusion is a stable intermediate of exocytosis. Dev. Cell 12 (2007) 653-659
49. Xu Y., Zhang F., Su Z., McNew J.A., and Shin Y.K. Hemifusion in SNARE-mediated membrane fusion. Nat. Struct. Mol. Biol. 12 (2005) 417-422
50. Yang L., and Huang H.W. Observation of a membrane fusion intermediate structure. Science 297 (2002) 1877-1879
51. 2+-triggered exocytosis. Neuron 34 (2002) 599-611
52. Zhou Z., Misler S., and Chow R.H. Rapid fluctuations in transmitter release from single vesicles in bovine adrenal chromaffin cells. Biophys. J. 70 (1996) 1543-1552
53. Zimmerberg J., Akimov S.A., and Frolov V. Synaptotagmin: fusogenic role for calcium sensor?. Nat. Struct. Mol. Biol. 13 (2006) 301-303