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Simultaneous Multicolor Multifocal Scanning Microscopy

delete2023-07-24
delete6
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OA
AI
K
Kyungduck Yoon
K
Keyi Han
K
Kidan Tadesse
B
Biagio Mandracchia
S
Shu Jia *
DOI:10.1021/acsphotonics.3c00205delete
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Abstract

Abstract

En 中文
Super-resolution fluorescence microscopy has revolutionizedcellbiology over the past decade, enabling the visualization of subcellularcomplexity with unparalleled clarity and detail. However, the rapiddevelopment of image-scanning-based super-resolution systems stillrestrains convenient access to commonly used instruments such as epi-fluorescencemicroscopes. Here, we present multifocal scanning microscopy (MSM)for super-resolution imaging with simultaneous multicolor acquisitionand minimal instrumental complexity. MSM implements a stationary,interposed multifocal multicolor excitation by exploiting the motionof the specimens, realizing super-resolution microscopy through ageneral epi-fluorescence platform without compromising the image-scanningmechanism or inducing complex instrument alignment. The system isdemonstrated with various phantom and biological specimens, and theresults present effective resolution doubling, optical sectioning,and contrast enhancement. We anticipate MSM, as a highly accessibleand compatible super-resolution technique, to offer a promising methodologicalpathway for broad cell biological discoveries.
Keywords:
MSM
super-resolution systems
optical sectioning
super-resolution imaging
image-scanning microscopy
cell biology

Journal

ACS Photonics cover
ACS Photonics
IF:
6.7
Papers:
5.6K
Citations:
2.5W

Organization

E
Emory University
Scholars:
5.0W
Papers: 4.2W
Citations: 5.7W