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脂磷素α蛋白:突触成熟的支架分子。

Liprin-alpha proteins: scaffold molecules for synapse maturation.

作者信息

Spangler S A, Hoogenraad C C

机构信息

Department of Neuroscience, Erasmus Medical Center, P.O. Box 2040, 3000CA, Rotterdam, The Netherlands.

出版信息

Biochem Soc Trans. 2007 Nov;35(Pt 5):1278-82. doi: 10.1042/BST0351278.

Abstract

Synapses are specialized communication junctions between neurons whose plasticity provides the structural and functional basis for information processing and storage in the brain. Recent biochemical, genetic and imaging studies in diverse model systems are beginning to reveal the molecular mechanisms by which synaptic vesicles, ion channels, receptors and other synaptic components assemble to make a functional synapse. Recent evidence has shown that the formation and function of synapses are critically regulated by the liprin-alpha family of scaffolding proteins. The liprin-alphas have been implicated in pre- and post-synaptic development by recruiting synaptic proteins and regulating synaptic cargo transport. Here, we will summarize the diversity of liprin binding partners, highlight the factors that control the function of liprin-alphas at the synapse and discuss how liprin-alpha family proteins regulate synapse formation and synaptic transmission.

摘要

突触是神经元之间的特殊通讯连接,其可塑性为大脑中的信息处理和存储提供了结构和功能基础。最近在多种模型系统中进行的生物化学、遗传学和成像研究开始揭示突触小泡、离子通道、受体和其他突触成分组装形成功能性突触的分子机制。最近的证据表明,突触的形成和功能受到支架蛋白liprin-α家族的严格调控。liprin-α通过招募突触蛋白和调节突触货物运输,参与突触前和突触后的发育。在这里,我们将总结liprin结合伴侣的多样性,强调控制liprin-α在突触处功能的因素,并讨论liprin-α家族蛋白如何调节突触形成和突触传递。

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