DNA-Based Super-Resolution Microscopy: DNA-PAINT

被引:50
|
作者
Nieves, Daniel J. [1 ,2 ]
Gaus, Katharina [1 ,2 ]
Baker, Matthew A. B. [3 ,4 ]
机构
[1] Univ New South Wales, EMBL Australia Node Single Mol Sci, Sch Med Sci, Sydney, NSW 2052, Australia
[2] Univ New South Wales, ARC Ctr Excellence Adv Mol Imaging, Sydney, NSW 2052, Australia
[3] Univ New South Wales, Sch Biotechnol & Biomol Sci, Sydney, NSW 2052, Australia
[4] CSIRO Synthet Biol Future Sci Platform, GPO Box 2583, Brisbane, Qld 4001, Australia
来源
GENES | 2018年 / 9卷 / 12期
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
DNA origami; DNA PAINT; DNA; super-resolution microscopy; SMLM; fluorescence microscopy; GENETIC-CODE EXPANSION; FLUORESCENCE MICROSCOPY; MOLECULE; BINDING; CELLS; RECONSTRUCTION; FLUOROPHORES; RESOLUTION; CHEMISTRY; PROTEIN;
D O I
10.3390/genes9120621
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Super-resolution microscopies, such as single molecule localization microscopy (SMLM), allow the visualization of biomolecules at the nanoscale. The requirement to observe molecules multiple times during an acquisition has pushed the field to explore methods that allow the binding of a fluorophore to a target. This binding is then used to build an image via points accumulation for imaging nanoscale topography (PAINT), which relies on the stochastic binding of a fluorescent ligand instead of the stochastic photo-activation of a permanently bound fluorophore. Recently, systems that use DNA to achieve repeated, transient binding for PAINT imaging have become the cutting edge in SMLM. Here, we review the history of PAINT imaging, with a particular focus on the development of DNA-PAINT. We outline the different variations of DNA-PAINT and their applications for imaging of both DNA origamis and cellular proteins via SMLM. Finally, we reflect on the current challenges for DNA-PAINT imaging going forward.
引用
收藏
页数:14
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