Kinetics of synaptotagmin responses to Ca2+ and assembly with the core SNARE complex onto membranes

被引:218
作者
Davis, AF
Bai, JH
Fasshauer, D
Wolowick, MJ
Lewis, JL
Chapman, ER [1 ]
机构
[1] Univ Wisconsin, Sch Med, Dept Physiol, Madison, WI 53706 USA
[2] Max Planck Inst Biophys Chem, Dept Neurobiol, D-37077 Gottingen, Germany
关键词
D O I
10.1016/S0896-6273(00)80850-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The synaptic vesicle protein synaptotagmin I binds Ca2+ and is required for efficient neurotransmitter release. Here, we measure the response time of the C2 domains of synaptotagmin to determine whether synaptotagmin is fast enough to function as a Ca2+ sensor for rapid exocytosis. We report that synaptotagmin is "tuned" to sense Ca2+ concentrations that trigger neuronal exocytosis. The speed of response is unique to synaptotagmin I and readily satisfies the kinetic constraints of synaptic vesicle membrane fusion. We further demonstrate that Ca2+ triggers penetration of synaptotagmin into membranes and simultaneously drives assembly of synaptotagmin onto the base of the ternary SNARE (soluble N-ethylmaleimide-sensitive fusion protein [NSF] attachment receptor) complex, near the transmembrane anchor of syntaxin. These data support a molecular model in which synaptotagmin triggers exocytosis through its interactions with membranes and the SNARE complex.
引用
收藏
页码:363 / 376
页数:14
相关论文
共 59 条
[31]   CALCIUM-DEPENDENCE OF NEUROTRANSMITTER RELEASE AND RATE OF SPONTANEOUS VESICLE FUSIONS ARE ALTERED IN DROSOPHILA SYNAPTOTAGMIN MUTANTS [J].
LITTLETON, JT ;
STERN, M ;
PERIN, M ;
BELLEN, HJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (23) :10888-10892
[32]   Synaptic function modulated by changes in the ratio of synaptotagmin I and IV [J].
Littleton, JT ;
Serano, TL ;
Rubin, GM ;
Ganetzky, B ;
Chapman, ER .
NATURE, 1999, 400 (6746) :757-760
[33]   Temperature-sensitive paralytic mutations demonstrate that synaptic exocytosis requires SNARE complex assembly and disassembly [J].
Littleton, JT ;
Chapman, ER ;
Kreber, R ;
Garment, MB ;
Carlson, SD ;
Ganetzky, B .
NEURON, 1998, 21 (02) :401-413
[34]   RELATIONSHIP BETWEEN PRESYNAPTIC CALCIUM CURRENT AND POSTSYNAPTIC POTENTIAL IN SQUID GIANT SYNAPSE [J].
LLINAS, R ;
STEINBERG, IZ ;
WALTON, K .
BIOPHYSICAL JOURNAL, 1981, 33 (03) :323-351
[35]   KINETICS OF ANNEXIN-VI, CALCIUM, AND PHOSPHOLIPID ASSOCIATION AND DISSOCIATION [J].
LU, Y ;
BAZZI, MD ;
NELSESTUEN, GL .
BIOCHEMISTRY, 1995, 34 (34) :10777-10785
[36]  
MIZUTA M, 1994, J BIOL CHEM, V269, P11675
[37]   Location of the membrane-docking face on the Ca2+-activated C2 domain of cytosolic phospholipase A2 [J].
Nalefski, EA ;
Falke, JJ .
BIOCHEMISTRY, 1998, 37 (51) :17642-17650
[38]   Ca2+-signaling cycle of a membrane-docking C2 domain [J].
Nalefski, EA ;
Slazas, MM ;
Falke, JJ .
BIOCHEMISTRY, 1997, 36 (40) :12011-12018
[39]   Syntaxin 1A inhibits CFTR chloride channels by means of domain-specific protein-protein interactions [J].
Naren, AP ;
Quick, MW ;
Collawn, JF ;
Nelson, DJ ;
Kirk, KL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (18) :10972-10977
[40]   SYNAPTIC FUNCTION IS IMPAIRED BUT NOT ELIMINATED IN C-ELEGANS MUTANTS LACKING SYNAPTOTAGMIN [J].
NONET, ML ;
GRUNDAHL, K ;
MEYER, BJ ;
RAND, JB .
CELL, 1993, 73 (07) :1291-1305