荧光团
显微镜
扫描电镜
纳米技术
光激活定位显微镜
超分辨显微术
荧光
图像分辨率
荧光显微镜
分辨率(逻辑)
纳米
超分辨率
计算机科学
物理
材料科学
人工智能
光学
受激发射
激光器
计算机视觉
图像(数学)
作者
Klaus Gwosch,Jasmin K. Pape,Francisco Balzarotti,Philipp Hoess,Jan Ellenberg,Jonas Ries,Stefan W. Hell
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2020-01-13
卷期号:17 (2): 217-224
被引量:506
标识
DOI:10.1038/s41592-019-0688-0
摘要
The ultimate goal of biological super-resolution fluorescence microscopy is to provide three-dimensional resolution at the size scale of a fluorescent marker. Here we show that by localizing individual switchable fluorophores with a probing donut-shaped excitation beam, MINFLUX nanoscopy can provide resolutions in the range of 1 to 3 nm for structures in fixed and living cells. This progress has been facilitated by approaching each fluorophore iteratively with the probing-donut minimum, making the resolution essentially uniform and isotropic over scalable fields of view. MINFLUX imaging of nuclear pore complexes of a mammalian cell shows that this true nanometer-scale resolution is obtained in three dimensions and in two color channels. Relying on fewer detected photons than standard camera-based localization, MINFLUX nanoscopy is poised to open a new chapter in the imaging of protein complexes and distributions in fixed and living cells. Advances in MINFLUX nanoscopy enable multicolor imaging over large fields of view, bringing true nanometer-scale fluorescence imaging to labeled structures in fixed and living cells.
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