stimulated emission depletion (STED)

受激发射损耗 (STED)
  • 文章类型: Journal Article
    CTP合酶(CTPS)可以在生命的所有三个域中的细胞中形成丝状结构,称为胞嘧啶。为了研究胞嘧啶的中尺度结构,我们在人类细胞中进行光漂白(FRAP)和受激发射损耗(STED)显微镜检查后进行荧光恢复。通过使用EGFP二聚体标签作为工具来探索胞质的物理性质,我们发现胞质是动态的和网状的。CTPS胞质的网状结构可能为其他成分提供空间,比如IMPDH。此外,我们观察到有触手的CTPS颗粒。
    CTP synthase (CTPS) can form filamentous structures termed cytoophidia in cells in all three domains of life. In order to study the mesoscale structure of cytoophidia, we perform fluorescence recovery after photobleaching (FRAP) and stimulated emission depletion (STED) microscopy in human cells. By using an EGFP dimeric tag as a tool to explore the physical properties of cytoophidia, we find that cytoophidia are dynamic and reticular. The reticular structure of CTPS cytoophidia may provide space for other components, such as IMPDH. In addition, we observe CTPS granules with tentacles.
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  • 文章类型: Journal Article
    在NIR中发射用于以超分辨率跟踪线粒体pH改变的小分子有望在生物医学应用中发挥重要作用。在这里,合成并系统地研究了两种基于吡啶盐的小分子(P1和P2)。发现吡啶盐P1和P2在NIR(约610nm)中发射,该方法可检测pH在2.0到11.0之间的变化,线性良好,灵敏度高。重要的是,P2可以在受激发射耗竭(STED)下以实时方式精确靶向细胞线粒体。这些结果暗示了在超分辨率成像和线粒体pH测定中具有潜在应用的化学策略。
    Small molecules emitting in the NIR for tracking mitochondrial pH alteration with super-resolution are expected to play an essential role in biomedical applications. Herein, two small molecules based on pyridinium salt (P1 and P2) have been synthesized and systematically investigated. It was found that pyridinium salts P1 and P2 emitted in the NIR (about 610 nm), which could detect pH changes from 2.0 to 11.0 with good linearity and high sensitivity. Importantly, P2 could precisely target cellular mitochondria in a real-time manner under stimulated emission depletion (STED). These results implied a chemical strategy with a potential application in super-resolution imaging and mitochondrial pH determination.
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