Toward quantitative fluorescence microscopy with DNA origami nanorulers

被引:10
作者
Beater, Susanne [1 ,2 ]
Raab, Mario [1 ,2 ]
Tinnefeld, Philip [1 ,2 ]
机构
[1] Braunschweig Univ Technol, Inst Phys & Theoret Chem, Braunschweig, Germany
[2] Braunschweig Integrated Ctr Syst Biol, Braunschweig, Germany
来源
QUANTITATIVE IMAGING IN CELL BIOLOGY | 2014年 / 123卷
关键词
STRUCTURED-ILLUMINATION MICROSCOPY; OPTICAL RECONSTRUCTION MICROSCOPY; SUPERRESOLUTION MICROSCOPY; STIMULATED-EMISSION; SINGLE-MOLECULE; LOCALIZATION MICROSCOPY; RESOLUTION LIMIT; NANOSCALE SHAPES; STED MICROSCOPY; FOCAL-PLANE;
D O I
10.1016/B978-0-12-420138-5.00024-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The dynamic development of fluorescence microscopy has created a large number of new techniques, many of which are able to overcome the diffraction limit. This chapter describes the use of DNA origami nanostructures as scaffold for quantifying microscope properties such as sensitivity and resolution. The DNA origami technique enables placing of a defined number of fluorescent dyes in programmed geometries. We present a variety of DNA origami nanorulers that include nanorulers with defined labeling density and defined distances between marks. The chapter summarizes the advantages such as practically free choice of dyes and labeling density and presents examples of nanorulers in use. New triangular DNA origami nanorulers that do not require photoinduced switching by imaging transient binding to DNA nanostructures are also reported. Finally, we simulate fluorescence images of DNA origami nanorulers and reveal that the optimal DNA nanoruler for a specific application has an intermark distance that is roughly 1.3-fold the expected optical resolution.
引用
收藏
页码:449 / 466
页数:18
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