scholarly journals Isotropic image in structured illumination microscopy patterned with a spatial light modulator

2009 ◽  
Vol 17 (17) ◽  
pp. 14710 ◽  
Author(s):  
Bo-Jui Chang ◽  
Li-Jun Chou ◽  
Yun-Ching Chang ◽  
Su-Yu Chiang
2014 ◽  
Vol 20 (S3) ◽  
pp. 388-389
Author(s):  
Zdeněk Švindrych ◽  
Pavel Křížek ◽  
Evgeny Smirnov ◽  
Martin Ovesný ◽  
Josef Borkovec ◽  
...  

2020 ◽  
Vol 10 (12) ◽  
pp. 4396
Author(s):  
Liang Feng ◽  
Xiaolei Wang ◽  
Xinlei Sun ◽  
Sende Wang ◽  
Lie Lin ◽  
...  

We demonstrated an efficient system for multifocal structured illumination microscopy (MSIM) utilizing a spatial light modulator (SLM). Nine phase profiles of chessboard phase plates loaded on the SLM in sequence are used to generate nine multifocal arrays on the focal plane. Subsequently, nine raw multifocal images are acquired. Finally, by extracting the parameters of the illumination patterns from the raw images precisely, a final super-resolved image is reconstructed by performing the standard reconstruction procedure of structured illumination microscopy (SIM). Our MSIM system realized nearly a 1.5-fold enhancement in spatial resolution compared with wide-field (WF) microscopy. The feasibility of the present system is validated on experiments and the results show its great performances along with good compatibility.


2014 ◽  
Vol 22 (17) ◽  
pp. 20663 ◽  
Author(s):  
Ronny Förster ◽  
Hui-Wen Lu-Walther ◽  
Aurélie Jost ◽  
Martin Kielhorn ◽  
Kai Wicker ◽  
...  

Author(s):  
Craig T. Russell ◽  
Michael Shaw

Since the first practical super-resolution structured illumination fluorescence microscopes (SIM) were demonstrated more than two decades ago, the method has become increasingly popular for a wide range of bioimaging applications. The high cost and relative inflexibility of commercial systems, coupled with the conceptual simplicity of the approach and the desire to exploit and customize existing hardware, have led to the development of a large number of home-built systems. Several detailed hardware designs are available in the scientific literature, complemented by open-source software tools for SIM image validation and reconstruction. However, there remains a lack of simple open-source software to control these systems and manage the synchronization between hardware components, which is critical for effective SIM imaging. This article describes a new suite of software tools based on the popular Micro-Manager package, which enable the keen microscopist to develop and run a SIM system. We use the software to control two custom-built, high-speed, spatial light modulator-based SIM systems, evaluating their performance by imaging a range of fluorescent samples. By simplifying the process of SIM hardware development, we aim to support wider adoption of the technique. This article is part of the Theo Murphy meeting issue ‘Super-resolution structured illumination microscopy (part 1)’.


2021 ◽  
Author(s):  
Craig T. Russell ◽  
Michael Shaw

SummarySince the first practical super-resolution structured illumination fluorescence microscopes (SIM) were demonstrated more than two decades ago the method has become increasingly popular for a wide range of bioimaging applications. The high cost and relative inflexibility of commercial systems, coupled with the conceptual simplicity of the approach and the desire to exploit and customise existing hardware, have led to the development of a large number of home-built systems. Several detailed hardware designs are available in the scientific literature, complemented by open-source software tools for SIM image validation and reconstruction. However, there remains a lack of simple open-source software to control these systems and manage the synchronization between hardware components, which is critical for effective SIM imaging. This article describes a new suite of software tools based on the popular Micro-Manager package, which enable the keen microscopist to develop and run a SIM system. We use the software to control two custom-built, high-speed, spatial light modulator-based SIM systems, evaluating their performance by imaging a range of fluorescent samples. By simplifying the process of SIM hardware development, we aim to support wider adoption of the technique.


2019 ◽  
Vol 9 (6) ◽  
pp. 1188 ◽  
Author(s):  
Verena Richter ◽  
Mathis Piper ◽  
Michael Wagner ◽  
Herbert Schneckenburger

In the context of various approaches to super-resolution microscopy, structured illumination microscopy (SIM) offers several advantages: it needs rather low light doses (with a low risk of phototoxicity or photobleaching), is comparably fast and flexible concerning the use of microscopes, objective lenses and cameras, and has potential for 3D imaging. This paper describes an experimental setup for SIM with first diffraction orders of a spectral light modulator (SLM) creating an interference pattern in two dimensions. We kept this system rather compact with a comparably large illuminated object field, validated it with nano-beads and applied it further to living cells for imaging the cytoskeleton, mitochondria or cell nuclei with a resolution slightly above 100 nm. Its advantages, challenges and limitations—concerning cameras, acquisition time, depth of imaging, light exposure, and combining it with further super-resolving methods—are discussed.


Sign in / Sign up

Export Citation Format

Share Document