荧光
高尔基体
荧光显微镜
荧光寿命成像显微镜
内质网
纳米尺度
显微镜
显微镜
生物物理学
细胞器
活体细胞成像
纳米技术
分辨率(逻辑)
电子显微镜
材料科学
化学
生物
光学
计算机科学
物理
细胞
生物化学
人工智能
作者
Yongdeng Zhang,Lena K. Schroeder,Mark D. Lessard,P. Kidd,Jeeyun Chung,Yuanbin Song,Lorena Benedetti,Yiming Li,Jonas Ries,Jonathan B. Grimm,Luke D. Lavis,Pietro De Camilli,James E. Rothman,David Baddeley,Joerg Bewersdorf
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2020-01-06
卷期号:17 (2): 225-231
被引量:108
标识
DOI:10.1038/s41592-019-0676-4
摘要
Combining the molecular specificity of fluorescent probes with three-dimensional imaging at nanoscale resolution is critical for investigating the spatial organization and interactions of cellular organelles and protein complexes. We present a 4Pi single-molecule switching super-resolution microscope that enables ratiometric multicolor imaging of mammalian cells at 5-10-nm localization precision in three dimensions using 'salvaged fluorescence'. Imaging two or three fluorophores simultaneously, we show fluorescence images that resolve the highly convoluted Golgi apparatus and the close contacts between the endoplasmic reticulum and the plasma membrane, structures that have traditionally been the imaging realm of electron microscopy. The salvaged fluorescence approach is equally applicable in most single-objective microscopes.
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