显微镜
荧光显微镜
多细胞生物
扫描电镜
超分辨率
分辨率(逻辑)
超分辨显微术
光激活定位显微镜
纳米尺度
蛋白质丝
显微镜
生物物理学
纳米技术
生物
光学
荧光
材料科学
细胞
物理
计算机科学
图像(数学)
遗传学
人工智能
作者
Pierre Bon,Jeanne Linarès-Loyez,Maxime Feyeux,Kévin Alessandri,Brahim Lounis,Pierre Nassoy,Laurent Cognet
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2018-04-27
卷期号:15 (6): 449-454
被引量:109
标识
DOI:10.1038/s41592-018-0005-3
摘要
Fluorescence localization microscopy has achieved near-molecular resolution capable of revealing ultra-structures, with a broad range of applications, especially in cellular biology. However, it remains challenging to attain such resolution in three dimensions and inside biological tissues beyond the first cell layer. Here we introduce SELFI, a framework for 3D single-molecule localization within multicellular specimens and tissues. The approach relies on self-interference generated within the microscope's point spread function (PSF) to simultaneously encode equiphase and intensity fluorescence signals, which together provide the 3D position of an emitter. We combined SELFI with conventional localization microscopy to visualize F-actin 3D filament networks and reveal the spatial distribution of the transcription factor OCT4 in human induced pluripotent stem cells at depths up to 50 µm inside uncleared tissue spheroids. SELFI paves the way to nanoscale investigations of native cellular processes in intact tissues.
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