Wide-Field Multispectral Super-Resolution Imaging Using Spin-Dependent Fluorescence in Nanodiamonds

Nano Letters ◽  
2013 ◽  
Vol 13 (5) ◽  
pp. 2073-2077 ◽  
Author(s):  
Edward H. Chen ◽  
Ophir Gaathon ◽  
Matthew E. Trusheim ◽  
Dirk Englund
2018 ◽  
Author(s):  
Robin Van den Eynde ◽  
Alice Sandmeyer ◽  
Wim Vandenberg ◽  
Sam Duwé ◽  
Wolfgang Hübner ◽  
...  

AbstractSuper-Resolution (SR) fluorescence microscopy is typically carried out on high-end research microscopes. Super-resolution Optical Fluctuation Imaging (SOFI) is a fast SR technique capable of live-cell imaging, that is compatible with many wide-field microscope systems. However, especially when employing fluorescent proteins, a key part of the imaging system is a very sensitive and well calibrated camera sensor. The substantial costs of such systems preclude many research groups from employing super-resolution imaging techniques.Here, we examine to what extent SOFI can be performed using a range of imaging hardware comprising different technologies and costs. In particular, we quantitatively compare the performance of an industry-grade CMOS camera to both state-of-the-art emCCD and sCMOS detectors, with SOFI-specific metrics. We show that SOFI data can be obtained using a cost-efficient industry-grade sensor, both on commercial and home-built microscope systems, though our analysis also readily exposes the merits of the per-pixel corrections performed in scientific cameras.


Molecules ◽  
2019 ◽  
Vol 24 (9) ◽  
pp. 1833 ◽  
Author(s):  
Iman Abdollahzadeh ◽  
Johnny Hendriks ◽  
Julia L. Sanwald ◽  
Indra M. Simons ◽  
Silke Hoffmann ◽  
...  

Subcellular structures containing autophagy-related proteins of the Atg8 protein family have been investigated with conventional wide-field fluorescence and single molecule localisation microscopy. Fusion proteins of GABARAP and LC3B, respectively, with EYFP were overexpressed in HEK293 cells. While size distributions of structures labelled by the two proteins were found to be similar, shape distributions appeared quite disparate, with EYFP-GABARAP favouring circular structures and elliptical structures being dominant for EYFP-LC3B. The latter also featured a nearly doubled fraction of U-shape structures. The experimental results point towards highly differential localisation of the two proteins, which appear to label structures representing distinct stages or even specific channels of vesicular trafficking pathways. Our data also demonstrate that the application of super-resolution techniques expands the possibilities of fluorescence-based methods in autophagy studies and in some cases can rectify conclusions obtained from conventional fluorescence microscopy with diffraction-limited resolution.


Nanoscale ◽  
2014 ◽  
Vol 6 (11) ◽  
pp. 5807-5812 ◽  
Author(s):  
Joseph Louis Ponsetto ◽  
Feifei Wei ◽  
Zhaowei Liu

Fluorescent imaging resolution down to 51 nm is shown by generating tunable localized plasmon excitations on a nano-antenna array.


CLEO: 2013 ◽  
2013 ◽  
Author(s):  
Edward H. Chen ◽  
Ophir Gaathon ◽  
Matthew E. Trusheim ◽  
Dirk R. Englund

Nanoscale ◽  
2019 ◽  
Vol 11 (4) ◽  
pp. 1737-1744 ◽  
Author(s):  
Yan Xi ◽  
Dianbing Wang ◽  
Tingting Wang ◽  
Lin Huang ◽  
Xian-En Zhang

Single particle protein on the AML cell membrane. Wide field image (left); SIM original image (middle); SIM 3D-reconstuction image (right).


2021 ◽  
Vol 9 (15) ◽  
pp. 2170058
Author(s):  
Hajun Yoo ◽  
Hongki Lee ◽  
Woo Joong Rhee ◽  
Gwiyeong Moon ◽  
Changhun Lee ◽  
...  

Author(s):  
Göran Maconi ◽  
Ivo Laidmäe ◽  
Ivan Kassamakov ◽  
Anton Nolvi ◽  
Jyrki Heinämäki ◽  
...  

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Shun Cao ◽  
Taisheng Wang ◽  
Wenbin Xu ◽  
Hua Liu ◽  
Hongxin Zhang ◽  
...  

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