High-density three-dimensional localization microscopy across large volumes

被引:0
|
作者
Legant, Wesley R. [1 ]
Shao, Lin [1 ]
Grimm, Jonathan B. [1 ]
Brown, Timothy A. [1 ]
Milkie, Daniel E. [1 ,2 ]
Avants, Brian B. [3 ,4 ]
Lavis, Luke D. [1 ]
Betzig, Eric [1 ]
机构
[1] Howard Hughes Med Inst, Janelia Res Campus, Ashburn, VA USA
[2] Coleman Technol, Newtown Sq, PA USA
[3] Univ Penn, PICSL, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Radiol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
GENETICALLY EXPRESSED PROBES; THICK BIOLOGICAL SAMPLES; WHOLE-CELL; LIVE CELLS; SUPERRESOLUTION MICROSCOPY; STRUCTURED ILLUMINATION; ELECTRON-MICROSCOPY; RESOLUTION; REVEALS; ORGANIZATION;
D O I
10.1038/NMETH.3797
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Extending three-dimensional (3D) single-molecule localization microscopy away from the coverslip and into thicker specimens will greatly broaden its biological utility. However, because of the limitations of both conventional imaging modalities and conventional labeling techniques, it is a challenge to localize molecules in three dimensions with high precision in such samples white simultaneously achieving the labeling densities required for high resolution of densely crowded structures. Here we combined lattice light-sheet microscopy with newly developed, freely diffusing, cell-permeable chemical probes with targeted affinity for DNA, intracellular membranes or the plasma membrane. We used this combination to perform high localization precision, ultrahigh-labeling density, multicolor localization microscopy in samples up to 20 pin thick, including dividing cells and the neuromast organ of a zebrafish embryo. We also demonstrate super-resolution correlative imaging with protein-specific photoactivable fluorophores, providing a mutually compatible, single-platform alternative to correlative light-electron microscopy over large volumes.
引用
收藏
页码:359 / 365
页数:7
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