3D reconstruction of high-resolution STED microscope images

被引:73
作者
Punge, Annedore [1 ]
Rizzoli, Silvio O. [2 ]
Jahn, Reinhard [2 ]
Wildanger, Jan Dominik [1 ]
Meyer, Lars [1 ]
Schoenle, Andreas [1 ]
Kastrup, Lars [1 ]
Hell, Stefan W. [1 ]
机构
[1] Max Planck Inst Biophys Chem, Dept NanoBiophoton, D-37077 Gottingen, Germany
[2] Max Planck Inst Biophys Chem, Dept Neurobiol, D-37077 Gottingen, Germany
关键词
STED; fluorescence; resolution; sectioning;
D O I
10.1002/jemt.20602
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Tackling biological problems often involves the imaging and localization of cellular structures on the nanometer scale. Although optical super-resolution below 100 nm can be readily attained with stimulated emission depletion (STED) and photoswitching microscopy methods, attaining an axial resolution <100 nm with focused light generally required the use of two lenses in a 4Pi configuration or exceptionally bright photochromic fluorophores. Here, we describe a simple technical solution for 3D nanoscopy of fixed samples: biological specimens are fluorescently labeled, embedded in a polymer resin, cut into thin sections, and then imaged via STED microscopy with nanoscale resolution. This approach allows a 3D image reconstruction with a resolution <80 nm in all directions using available state-of-the art STED microscopes.
引用
收藏
页码:644 / 650
页数:7
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