S. R. Pfeffer, Unsolved mysteries in membrane traffic, Annu Rev Biochem, vol.76, pp.629-645, 2007.

M. G. Waters and F. M. Hughson, Membrane tethering and fusion in the secretory and endocytic pathways, Traffic, vol.1, pp.588-597, 2000.

P. I. Hanson, R. Roth, H. Morisaki, R. Jahn, and J. E. Heuser, Structure and conformational changes in NSF, its membrane receptor complexes visualized by quick-freeze/deepetch electron microscopy, Cell, vol.90, pp.523-535, 1997.

C. Hu, Fusion of cells by flipped SNAREs, Science, vol.300, pp.1745-1749, 2003.

F. Li, Energetics and dynamics of SNAREpin folding across lipid bilayers, Nat Struct Mol Biol, vol.14, pp.890-896, 2007.
URL : https://hal.archives-ouvertes.fr/inserm-02296629

T. J. Melia, Regulation of membrane fusion by the membrane-proximal coil of the t-SNARE during zippering of SNAREpins, J Cell Biol, vol.158, pp.929-940, 2002.

T. Sollner, M. K. Bennett, S. W. Whiteheart, R. H. Scheller, and J. E. Rothman, A protein assembly-disassembly pathway in-vitro that may correspond to sequential steps of synaptic vesicle docking, activation, and fusion, Cell, vol.75, pp.409-418, 1993.

T. Weber, SNAREpins: Minimal machinery for membrane fusion, Cell, vol.92, pp.759-772, 1998.

R. D. Burgoyne and A. Morgan, Membrane trafficking: Three steps to fusion, Curr Biol, vol.17, pp.255-258, 2007.

J. Rizo and T. C. Sudhof, SNAREs and Munc18 in synaptic vesicle fusion, Nat Rev Neurosci, vol.3, pp.641-653, 2002.

R. F. Toonen and M. Verhage, Munc18-1 in secretion: Lonely Munc joins SNARE team and takes control, Trends Neurosci, vol.30, pp.564-572, 2007.

I. Dulubova, A conformational switch in syntaxin during exocytosis: Role of munc18, EMBO J, vol.18, pp.4372-4382, 1999.

Y. Hata, C. A. Slaughter, and T. C. Sudhof, Synaptic vesicle fusion complex contains unc-18 homolog bound to syntaxin, Nature, vol.366, pp.347-351, 1993.

K. M. Misura, R. H. Scheller, and W. I. Weis, Three-dimensional structure of the neuronalSec1-syntaxin 1a complex, Nature, vol.404, pp.355-362, 2000.

I. Dulubova, Munc18-1 binds directly to the neuronal SNARE complex, Proc Natl Acad Sci, vol.104, pp.2697-2702, 2007.

C. Rickman, C. N. Medine, A. Bergmann, and R. R. Duncan, Functionally and spatially distinct modes of munc18-syntaxin 1 interaction, J Biol Chem, vol.282, pp.12097-12103, 2007.

J. S. Shen, D. C. Tareste, F. Paumet, J. E. Rothman, and T. J. Melia, Selective activation of cognate SNAREpins by Sec1/Munc18 proteins, Cell, vol.128, pp.183-195, 2007.
URL : https://hal.archives-ouvertes.fr/inserm-02296593

B. L. Scott, Sec1p directly stimulates SNARE-mediated membrane fusion in vitro, J Cell Biol, vol.167, pp.75-85, 2004.

J. A. Mcnew, Close is not enough: SNARE-dependent membrane fusion requires an active mechanism that transduces force to membrane anchors, J Cell Biol, vol.150, pp.105-117, 2000.

K. Hu, Vesicular restriction of synaptobrevin suggests a role for calcium in membrane fusion, Nature, vol.415, pp.646-650, 2002.

C. G. Schuette, Determinants of liposome fusion mediated by synaptic SNARE proteins, Proc Natl Acad Sci, vol.101, pp.2858-2863, 2004.

W. C. Tucker, T. Weber, and E. R. Chapman, Reconstitution of Ca 2? -regulated membrane fusion by synaptotagmin and SNAREs, Science, vol.304, pp.435-438, 2004.

X. Lu, F. Zhang, J. A. Mcnew, and Y. K. Shin, Membrane fusion induced by neuronal SNAREs transits through hemifusion, J Biol Chem, vol.280, pp.30538-30541, 2005.

T. J. Melia, D. Q. You, D. C. Tareste, and J. E. Rothman, Lipidic antagonists to SNAREmediated fusion, J Biol Chem, vol.281, pp.29597-29605, 2006.
URL : https://hal.archives-ouvertes.fr/inserm-02296596

J. Vicogne, Asymmetric phospholipid distribution drives in vitro reconstituted SNARE-dependent membrane fusion, Proc Natl Acad Sci, vol.103, pp.14761-14766, 2006.

K. Bacia, C. G. Schuette, N. Kahya, R. Jahn, and P. Schwille, SNAREs prefer liquiddisordered over ''raft'' (liquid-ordered) domains when reconstituted into giant unilamellar vesicles, J Biol Chem, vol.279, pp.37951-37955, 2004.

M. K. Doeven, Distribution, lateral mobility and function of membrane proteins incorporated into giant unilamellar vesicles, Biophys J, vol.88, pp.1134-1142, 2005.

P. Girard, A new method for the reconstitution of membrane proteins into giant unilamellar vesicles, Biophys J, vol.87, pp.419-429, 2004.
URL : https://hal.archives-ouvertes.fr/hal-00314159

J. B. Manneville, P. Bassereau, D. Levy, and J. Prost, Activity of transmembrane proteins induces magnification of shape fluctuations of lipid membranes, Phys Rev Lett, vol.82, pp.4356-4359, 1999.

J. L. Rigaud and D. Levy, Reconstitution of membrane proteins into liposomes, Methods Enzymol, vol.372, pp.65-86, 2003.

S. Takamori, Molecular anatomy of a trafficking organelle, Cell, vol.127, pp.831-846, 2006.

V. Marchi-artzner, Selective adhesion, lipid exchange and membranefusion processes between vesicles of various sizes bearing complementary molecular recognition groups, ChemPhysChem, vol.2, pp.367-376, 2001.

N. Kahya, E. I. Pecheur, W. P. De-boeij, D. A. Wiersma, and D. Hoekstra, Reconstitution of membrane proteins into giant unilamellar vesicles via peptide-induced fusion, Biophys J, vol.81, pp.1464-1474, 2001.
URL : https://hal.archives-ouvertes.fr/hal-00314404

S. Nir, J. Wilschut, and J. Bentz, The rate of fusion of phospholipid-vesicles and the role of bilayer curvature, Biochim Biophys Acta, vol.688, pp.275-278, 1982.

B. R. Lentz, G. F. Mcintyre, D. J. Parks, J. C. Yates, and D. Massenburg, Bilayer curvature and certain amphipaths promote poly(ethylene glycol)-induced fusion of dipalmitoylphosphatidylcholine unilamellar vesicles, Biochemistry, vol.31, pp.2643-2653, 1992.

F. Nomura, Microscopic observations reveal that fusogenic peptides induce liposome shrinkage prior to membrane fusion, Proc Natl Acad Sci, vol.101, pp.3420-3425, 2004.

T. Lang, SNAREs are concentrated in cholesterol-dependent clusters that define docking and fusion sites for exocytosis, EMBO J, vol.20, pp.2202-2213, 2001.

J. J. Sieber, K. I. Willig, R. Heintzmann, S. W. Hell, and T. Lang, The SNARE motif is essential for the formation of syntaxin clusters in the plasma membrane, Biophys J, vol.90, pp.2843-2851, 2006.

T. Baumgart, S. T. Hess, and W. W. Webb, Imaging coexisting fluid domains in biomembrane models coupling curvature and line tension, Nature, vol.425, pp.821-824, 2003.

M. Verhage, Synaptic assembly of the brain in the absence of neurotransmitter secretion, Science, vol.287, pp.864-869, 2000.

S. D. Harrison, K. Broadie, J. Vandegoor, and G. M. Rubin, Mutations in the drosophila rop gene suggest a function in general secretion and synaptic transmission, Neuron, vol.13, pp.555-566, 1994.

R. M. Weimer, Defects in synaptic vesicle docking in unc-18 mutants, Nat Neurosci, vol.6, pp.1023-1030, 2003.

T. J. Melia, Putting the clamps on membrane fusion: How complexin sets the stage for calcium-mediated exocytosis, FEBS Lett, vol.581, pp.2131-2139, 2007.

K. Braeckmans, L. Peeters, N. N. Sanders, D. Smedt, S. C. Demeester et al., Threedimensional fluorescence recovery after photobleaching with the confocal scanning laser microscope, Biophys J, vol.85, pp.2240-2252, 2003.

A. Lopez, L. Dupou, A. Altibelli, J. Trotard, and J. F. Tocanne, Critical comparison of analytical solutions, and a new mathematical method for calculation of diffusion coefficient D, Biophys J, vol.53, pp.963-970, 1988.