Membrane Fusion: Grappling with SNARE and SM Proteins

被引:1500
作者
Sudhof, Thomas C. [1 ]
Rothman, James E. [2 ]
机构
[1] Stanford Univ, Dept Cellular & Mol Physiol, Palo Alto, CA 94304 USA
[2] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06520 USA
关键词
SYNAPTIC VESICLE FUSION; NEUROTRANSMITTER RELEASE; 3-DIMENSIONAL STRUCTURE; SYNAPTOTAGMIN-I; PHOSPHOLIPID-BINDING; VESICULAR TRANSPORT; GOLGI-COMPLEX; YEAST; EXOCYTOSIS; IDENTIFICATION;
D O I
10.1126/science.1161748
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The two universally required components of the intracellular membrane fusion machinery, SNARE and SM (Sec1/Munc18- like) proteins, play complementary roles in fusion. Vesicular and target membrane- localized SNARE proteins zipper up into an alpha- helical bundle that pulls the two membranes tightly together to exert the force required for fusion. SM proteins, shaped like clasps, bind to trans- SNARE complexes to direct their fusogenic action. Individual fusion reactions are executed by distinct combinations of SNARE and SM proteins to ensure specificity, and are controlled by regulators that embed the SM- SNARE fusion machinery into a physiological context. This regulation is spectacularly apparent in the exquisite speed and precision of synaptic exocytosis, where synaptotagmin ( the calcium- ion sensor for fusion) cooperates with complexin ( the clamp activator) to control the precisely timed release of neurotransmitters that initiates synaptic transmission and underlies brain function.
引用
收藏
页码:474 / 477
页数:4
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