显微镜
生物物理学
细胞内
薄层荧光显微镜
各向同性
超分辨显微术
分辨率(逻辑)
材料科学
纳米技术
化学
生物
物理
光学
计算机科学
扫描共焦电子显微镜
人工智能
生物化学
作者
Yuxuan Zhao,Meng Zhang,Wenting Zhang,Yao Zhou,Longbiao Chen,Qing Liu,Peng Wang,Rong Chen,Xinxin Duan,Feifan Chen,Huan Deng,Yunfei Wei,Peng Fei,Yuhui Zhang
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2022-03-01
卷期号:19 (3): 359-369
被引量:87
标识
DOI:10.1038/s41592-022-01395-5
摘要
Long-term visualization of the dynamic interactions between intracellular structures throughout the three-dimensional space of whole live cells is essential to better understand their functions, but this task remains challenging due to the limitations of existing three-dimensional fluorescence microscopy techniques, such as an insufficient axial resolution, low volumetric imaging rate and photobleaching. Here, we present the combination of a progressive deep-learning super-resolution strategy with a double-ring-modulated selective plane illumination microscopy design capable of visualizing the dynamics of intracellular structures in live cells for hours at an isotropic spatial resolution of roughly 100 nm in three dimensions at speeds up to roughly 17 Hz. Using this approach, we reveal the complex spatial relationships and interactions between endoplasmic reticulum (ER) and mitochondria throughout live cells, providing new insights into ER-mediated mitochondrial division. We also examined the motion of Drp1 oligomers involved in mitochondrial fission and revealed the dynamic interactions between Drp1 and mitochondria in three dimensions.
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