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Interrogating Synaptic Architecture: Approaches for Labeling Organelles and Cytoskeleton Components

机译:询问突触结构:标记细胞器和细胞骨架成分的方法

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摘要

Synaptic transmission has been studied for decades, as a fundamental step in brain function. The structure of the synapse, and its changes during activity, turned out to be key aspects not only in the transfer of information between neurons, but also in cognitive processes such as learning and memory. The overall synaptic morphology has traditionally been studied by electron microscopy, which enables the visualization of synaptic structure in great detail. The changes in the organization of easily identified structures, such as the presynaptic active zone, or the postsynaptic density, are optimally studied via electron microscopy. However, few reliable methods are available for labeling individual organelles or protein complexes in electron microscopy. For such targets one typically relies either on combination of electron and fluorescence microscopy, or on super-resolution fluorescence microscopy. This review focuses on approaches and techniques used to specifically reveal synaptic organelles and protein complexes, such as cytoskeletal assemblies. We place the strongest emphasis on methods detecting the targets of interest by affinity binding, and we discuss the advantages and limitations of each method.
机译:突触传递已被研究了数十年,是大脑功能的基本步骤。突触的结构及其在活动过程中的变化,不仅是神经元之间信息传递的关键方面,而且在诸如学习和记忆等认知过程中也成为关键方面。传统上,通过电子显微镜研究了整个突触形态,这使得能够非常详细地观察突触结构。易于识别的结构(如突触前活动区或突触后密度)的组织变化是通过电子显微镜最佳研究的。但是,很少有可靠的方法可用于在电子显微镜中标记单个细胞器或蛋白质复合物。对于此类靶标,通常依赖于电子显微镜和荧光显微镜的组合,或超分辨率荧光显微镜。这篇综述的重点是用于专门揭示突触细胞器和蛋白质复合物(如细胞骨架装配体)的方法和技术。我们将重点放在通过亲和力绑定检测目标目标的方法上,并讨论每种方法的优点和局限性。

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