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Bassoon-disruption slows vesicle replenishment and induces homeostatic plasticity at a CNS synapse.巴松管缺失会减缓囊泡的补充,并诱导中枢神经系统突触的代偿性可塑性。
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CAPS and Munc13: CATCHRs that SNARE Vesicles.CAPS和Munc13:捕获小泡的SNARE蛋白。
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Liprin-α/SYD-2 determines the size of dense projections in presynaptic active zones in C. elegans.脂质连接蛋白-α/SYD-2 决定线虫突触前活性区致密突的大小。
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Molecular mechanisms for synchronous, asynchronous, and spontaneous neurotransmitter release.同步、异步和自发神经递质释放的分子机制。
Annu Rev Physiol. 2014;76:333-63. doi: 10.1146/annurev-physiol-021113-170338. Epub 2013 Nov 21.
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The Bruchpilot cytomatrix determines the size of the readily releasable pool of synaptic vesicles.布鲁赫飞行员细胞基质决定了突触囊泡可释放池的大小。
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Dynamic control of synaptic vesicle replenishment and short-term plasticity by Ca(2+)-calmodulin-Munc13-1 signaling.钙离子-钙调蛋白-Munc13-1 信号对突触囊泡补充和短期可塑性的动态控制。
Neuron. 2013 Jul 10;79(1):82-96. doi: 10.1016/j.neuron.2013.05.011. Epub 2013 Jun 13.
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Liprin-α2 promotes the presynaptic recruitment and turnover of RIM1/CASK to facilitate synaptic transmission.脂质连接蛋白-α2 促进 RIM1/CASK 在前突触的募集和周转,从而促进突触传递。
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Metabolic turnover of synaptic proteins: kinetics, interdependencies and implications for synaptic maintenance.突触蛋白的代谢周转率:动力学、相互依存关系及其对突触维持的影响。
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The Munc13 proteins differentially regulate readily releasable pool dynamics and calcium-dependent recovery at a central synapse.Munc13 蛋白在中枢突触中差异调节易释放池动力学和钙依赖性恢复。
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10
Molecular profiling of synaptic vesicle docking sites reveals novel proteins but few differences between glutamatergic and GABAergic synapses.突触小泡停泊位点的分子剖析揭示了新的蛋白,但谷氨酸能和 GABA 能突触之间鲜有差异。
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活跃区的大分子复合物:用于神经递质释放的集成纳米机器

Macromolecular complexes at active zones: integrated nano-machineries for neurotransmitter release.

作者信息

Chua John Jia En

机构信息

Department of Neurobiology, Max-Planck-Institute for Biophysical Chemistry, Am Fassberg 11, 37077, Göttingen, Germany,

出版信息

Cell Mol Life Sci. 2014 Oct;71(20):3903-16. doi: 10.1007/s00018-014-1657-5. Epub 2014 Jun 10.

DOI:10.1007/s00018-014-1657-5
PMID:24912984
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11113288/
Abstract

The release of neurotransmitters from synaptic vesicles exocytosing at presynaptic nerve terminals is a critical event in the initiation of synaptic transmission. This event occurs at specialized sites known as active zones. The task of faithfully executing various steps in the process is undertaken by careful orchestration of overlapping sets of molecular nano-machineries upon a core macromolecular scaffold situated at active zones. However, their composition remains incompletely elucidated. This review provides an overview of the role of the active zone in mediating neurotransmitter release and summarizes the recent progress using neuroproteomic approaches to decipher their composition. Key proteins of these nano-machineries are highlighted.

摘要

神经递质从突触前神经末梢处胞吐的突触小泡中释放,是突触传递起始过程中的一个关键事件。这一事件发生在被称为活性区的特化部位。该过程中各个步骤的精确执行任务,是由位于活性区的核心大分子支架上重叠的分子纳米机器集合精心编排完成的。然而,它们的组成仍未完全阐明。本综述概述了活性区在介导神经递质释放中的作用,并总结了使用神经蛋白质组学方法破译其组成的最新进展。重点介绍了这些纳米机器的关键蛋白质。