A molecular mechanism for calcium-mediated synaptotagmin-triggered exocytosis

被引:28
|
作者
Kiessling, Volker [1 ,2 ]
Kreutzberger, Alexj B. [1 ,2 ]
Liang, Binyong [1 ,2 ]
Nyenhuis, Sarah B. [3 ]
Seelheim, Patrick [1 ,2 ]
Castle, J. David [4 ]
Cafiso, David S. [3 ]
Tamm, Lukas K. [1 ,2 ]
机构
[1] Univ Virginia, Ctr Membrane & Cell Physiol, Charlottesville, VA 22903 USA
[2] Univ Virginia, Dept Mol Physiol & Biol Phys, Charlottesville, VA 22903 USA
[3] Univ Virginia, Dept Chem, Charlottesville, VA USA
[4] Univ Virginia, Dept Cell Biol, Charlottesville, VA USA
关键词
INTERFERENCE-CONTRAST MICROSCOPY; PLANAR SUPPORTED BILAYERS; SYNAPTIC VESICLE FUSION; NEURONAL SNARE COMPLEX; MEMBRANE-FUSION; NEUROTRANSMITTER RELEASE; PLASMA-MEMBRANE; TRANSMITTER RELEASE; OXIDIZED SILICON; LIPID-BILAYERS;
D O I
10.1038/s41594-018-0130-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The regulated exocytotic release of neurotransmitter and hormones is accomplished by a complex protein machinery whose core consists of SNARE proteins and the calcium sensor synaptotagmin-1. We propose a mechanism in which the lipid membrane is intimately involved in coupling calcium sensing to release. We found that fusion of dense core vesicles, derived from rat PC12 cells, was strongly linked to the angle between the cytoplasmic domain of the SNARE complex and the plane of the target membrane. We propose that, as this tilt angle increases, force is exerted on the SNARE transmembrane domains to drive the merger of the two bilayers. The tilt angle markedly increased following calcium-mediated binding of synaptotagmin to membranes, strongly depended on the surface electrostatics of the membrane, and was strictly coupled to the lipid order of the target membrane.
引用
收藏
页码:911 / +
页数:9
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