STED Imaging of Vesicular Endocytosis in the Synapse.

突触中囊泡内吞作用的STED成像

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作者:Hu Shaoqin, Xie Zhenli, Wang Bianbian, Chen Yang, Jing Zexin, Hao Ying, Yao Jingyu, Wu Xuanang, Huo Jingxiao, Wei Anqi, Qin Yuhao, Dong Nan, Zheng Chaowen, Song Qian, Long Jiangang, Kang Xinjiang, Wang Changhe, Xu Huadong
Endocytosis is a fundamental biological process that couples exocytosis to maintain the homeostasis of the plasma membrane and sustained neurotransmission. Super-resolution microscopy enables optical imaging of exocytosis and endocytosis in live cells and makes an essential contribution to understanding molecular mechanisms of endocytosis in neuronal somata and other types of cells. However, visualization of exo-endocytic events at the single vesicular level in a synapse with optical imaging remains a great challenge to reveal mechanisms governing the synaptic exo-endocytotic coupling. In this protocol, we describe the technical details of stimulated emission depletion (STED) imaging of synaptic endocytosis at the single-vesicle level, from sample preparation and microscopy calibration to data acquisition and analysis.

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