Britton Chance Center for Biomedical Photonics, Wuhan National Laboratory for Optoelectronics-Huazhong University of Science and Technology, Wuhan, Hubei, 430074, China.
MoE Key Laboratory for Biomedical Photonics, Collaborative Innovation Center for Biomedical Engineering, School of Engineering Sciences, Huazhong University of Science and Technology, Wuhan, Hubei, 430074, China.
Nat Commun. 2017 Nov 3;8(1):1307. doi: 10.1038/s41467-017-01503-6.
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.
在活细胞中对溶酶体和线粒体之间的长期纳米级相互作用进行特征化对于理解它们的功能至关重要,但由于现有荧光探针的局限性,这仍然具有挑战性。在这里,我们开发了具有优异特异性和高光稳定性的细胞通透性有机荧光探针用于溶酶体。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,我们在长达约 13 分钟的时间内以约 90nm 的分辨率获得了活细胞中动态物理溶酶体-线粒体相互作用的双色结构光照明显微镜(SIM)图像。我们成功地通过超分辨率成像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。我们的探针为理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一种途径。