Chip-based wide field-of-view nanoscopy

被引:0
|
作者
Diekmann, Robin [1 ]
Helle, Oystein I. [2 ]
Oie, Cristina I. [2 ]
McCourt, Peter [3 ]
Huser, Thomas R. [1 ,4 ,5 ]
Schuettpelz, Mark [1 ]
Ahluwalia, Balpreet S. [2 ]
机构
[1] Univ Bielefeld, Dept Phys, D-33615 Bielefeld, Germany
[2] UiT Arctic Univ Norway, Dept Phys & Technol, N-9037 Tromso, Norway
[3] UiT Arctic Univ Norway, Dept Med Biol, N-9037 Tromso, Norway
[4] Univ Calif Davis, Dept Internal Med, Davis, CA 95817 USA
[5] Univ Calif Davis, NSF Ctr Biophoton, Davis, CA 95817 USA
基金
欧洲研究理事会;
关键词
SINGLE-MOLECULE LOCALIZATION; OPTICAL RECONSTRUCTION MICROSCOPY; FLUORESCENCE MICROSCOPY; RESOLUTION LIMIT; CELLS; LIVER; EXCITATION; GUIDE; MICROPARTICLES; ILLUMINATION;
D O I
10.1038/NPHOTON.2017.55
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Present optical nanoscopy techniques use a complex microscope for imaging and a simple glass slide to hold the sample. Here, we demonstrate the inverse: the use of a complex, but mass-producible optical chip, which hosts the sample and provides a waveguide for the illumination source, and a standard low-cost microscope to acquire super-resolved images via two different approaches. Waveguides composed of a material with high refractive-index contrast provide a strong evanescent field that is used for single-molecule switching and fluorescence excitation, thus enabling chip-based single-molecule localization microscopy. Additionally, multimode interference patterns induce spatial fluorescence intensity variations that enable fluctuation-based super-resolution imaging. As chip-based nanoscopy separates the illumination and detection light paths, total-internal-reflection fluorescence excitation is possible over a large field of view, with up to 0.5 mm x 0.5 mm being demonstrated. Using multicolour chip-based nanoscopy, we visualize fenestrations in liver sinusoidal endothelial cells.
引用
收藏
页码:322 / +
页数:9
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