Calcium-dependent regulation of SNARE-mediated membrane fusion by calmodulin. - Archive ouverte HAL Access content directly
Journal Articles Journal of Biological Chemistry Year : 2010

Calcium-dependent regulation of SNARE-mediated membrane fusion by calmodulin.

(1) , (1) , (1) , (1, 2) , (1) , (1)
1
2

Abstract

Neuroexocytosis requires SNARE proteins, which assemble into trans complexes at the synaptic vesicle/plasma membrane interface and mediate bilayer fusion. Ca(2+) sensitivity is thought to be conferred by synaptotagmin, although the ubiquitous Ca(2+)-effector calmodulin has also been implicated in SNARE-dependent membrane fusion. To examine the molecular mechanisms involved, we examined the direct action of calmodulin and synaptotagmin in vitro, using fluorescence resonance energy transfer to assay lipid mixing between target- and vesicle-SNARE liposomes. Ca(2+)/calmodulin inhibited SNARE assembly and membrane fusion by binding to two distinct motifs located in the membrane-proximal regions of VAMP2 (K(D) = 500 nm) and syntaxin 1 (K(D) = 2 microm). In contrast, fusion was increased by full-length synaptotagmin 1 anchored in vesicle-SNARE liposomes. When synaptotagmin and calmodulin were combined, synaptotagmin overcame the inhibitory effects of calmodulin. Furthermore, synaptotagmin displaced calmodulin binding to target-SNAREs. These findings suggest that two distinct Ca(2+) sensors act antagonistically in SNARE-mediated fusion.

Dates and versions

inserm-00581206 , version 1 (30-03-2011)

Identifiers

Cite

Jerome Di Giovanni, Cécile Iborra, Yves Maulet, Christian Lévêque, Oussama El Far, et al.. Calcium-dependent regulation of SNARE-mediated membrane fusion by calmodulin.. Journal of Biological Chemistry, 2010, 285 (31), pp.23665-75. ⟨10.1074/jbc.M109.096073⟩. ⟨inserm-00581206⟩
112 View
0 Download

Altmetric

Share

Gmail Facebook Twitter LinkedIn More