首页> 外文期刊>Nature Communications >Cell-permeable organic fluorescent probes for live-cell long-term super-resolution imaging reveal lysosome-mitochondrion interactions
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Cell-permeable organic fluorescent probes for live-cell long-term super-resolution imaging reveal lysosome-mitochondrion interactions

机译:用于活细胞长期超分辨率成像的可渗透细胞的有机荧光探针显示溶酶体-线粒体相互作用

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Characterizing the long-term nanometer-scale interactions between lysosomes and mitochondria in live cells is essential for understanding their functions but remains challenging due to limitations of the existing fluorescent probes. Here, we develop cell-permeable organic fluorescent probes for lysosomes with excellent specificity and high photostability. We also use an existing Atto 647N dye with high brightness and excellent photostability to achieve specific labeling of mitochondria in live cells. Using these probes, we obtain dual-color structured illumination microscopy (SIM) images of dynamic physical lysosome-mitochondrion interactions in live cells at an ~90-nm resolution over a long time course of ~13?min. We successfully record the consecutive dynamic processes of lysosomal fusion and fission, as well as four types of physical lysosome-mitochondrion interactions by super-resolution imaging. Our probes provide an avenue for understanding the functions and the dynamic interplay of lysosomes and mitochondria in live cells.
机译:表征活细胞中溶酶体与线粒体之间的长期纳米级相互作用对于了解其功能至关重要,但由于现有荧光探针的局限性,仍然具有挑战性。在这里,我们开发了针对溶酶体的细胞渗透性有机荧光探针,具有出色的特异性和高光稳定性。我们还使用现有的具有高亮度和出色光稳定性的Atto 647N染料来实现活细胞中线粒体的特异性标记。使用这些探针,我们获得了双色结构照明显微镜(SIM)图像,该图像显示了活细胞中动态物理溶酶体-线粒体相互作用的动态过程,在〜13?min的长时间内,分辨率为〜90 nm。我们通过超分辨率成像成功地记录了溶酶体融合和裂变的连续动态过程,以及四种类型的物理溶酶体-线粒体相互作用。我们的探针为了解活细胞中溶酶体和线粒体的功能和动态相互作用提供了途径。

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