» Articles » PMID: 24706872

Two-photon Excitation Improves Multifocal Structured Illumination Microscopy in Thick Scattering Tissue

Overview
Specialty Science
Date 2014 Apr 8
PMID 24706872
Citations 35
Authors
Affiliations
Soon will be listed here.
Abstract

Multifocal structured illumination microscopy (MSIM) provides a twofold resolution enhancement beyond the diffraction limit at sample depths up to 50 µm, but scattered and out-of-focus light in thick samples degrades MSIM performance. Here we implement MSIM with a microlens array to enable efficient two-photon excitation. Two-photon MSIM gives resolution-doubled images with better sectioning and contrast in thick scattering samples such as Caenorhabditis elegans embryos, Drosophila melanogaster larval salivary glands, and mouse liver tissue.

Citing Articles

Optical sectioning methods in three-dimensional bioimaging.

Zhang J, Qiao W, Jin R, Li H, Gong H, Chen S Light Sci Appl. 2024; 14(1):11.

PMID: 39741128 PMC: 11688461. DOI: 10.1038/s41377-024-01677-x.


Mechanical-scan-free multicolor super-resolution imaging with diffractive spot array illumination.

Xu N, Bohndiek S, Li Z, Zhang C, Tan Q Nat Commun. 2024; 15(1):4135.

PMID: 38755150 PMC: 11099116. DOI: 10.1038/s41467-024-48482-z.


Superresolution structured illumination microscopy reconstruction algorithms: a review.

Chen X, Zhong S, Hou Y, Cao R, Wang W, Li D Light Sci Appl. 2023; 12(1):172.

PMID: 37433801 PMC: 10336069. DOI: 10.1038/s41377-023-01204-4.


Deep-MSIM: Fast Image Reconstruction with Deep Learning in Multifocal Structured Illumination Microscopy.

Liao J, Zhang C, Xu X, Zhou L, Yu B, Lin D Adv Sci (Weinh). 2023; 10(27):e2300947.

PMID: 37424045 PMC: 10520669. DOI: 10.1002/advs.202300947.


Microscopes in Conservative Dentistry and Endodontics Research.

Singh S J Conserv Dent. 2022; 25(4):333-337.

PMID: 36187867 PMC: 9520651. DOI: 10.4103/jcd.jcd_402_22.


References
1.
Nielsen T, Fricke M, Hellweg D, Andresen P . High efficiency beam splitter for multifocal multiphoton microscopy. J Microsc. 2001; 201(Pt 3):368-76. DOI: 10.1046/j.1365-2818.2001.00852.x. View

2.
Sandison D, Piston D, Williams R, Webb W . Quantitative comparison of background rejection, signal-to-noise ratio, and resolution in confocal and full-field laser scanning microscopes. Appl Opt. 2010; 34(19):3576-88. DOI: 10.1364/AO.34.003576. View

3.
Egner A, Jakobs S, Hell S . Fast 100-nm resolution three-dimensional microscope reveals structural plasticity of mitochondria in live yeast. Proc Natl Acad Sci U S A. 2002; 99(6):3370-5. PMC: 122530. DOI: 10.1073/pnas.052545099. View

4.
Straub M, Lodemann P, Holroyd P, Jahn R, Hell S . Live cell imaging by multifocal multiphoton microscopy. Eur J Cell Biol. 2000; 79(10):726-34. DOI: 10.1078/0171-9335-00105. View

5.
Edelstein A, Amodaj N, Hoover K, Vale R, Stuurman N . Computer control of microscopes using µManager. Curr Protoc Mol Biol. 2010; Chapter 14:Unit14.20. PMC: 3065365. DOI: 10.1002/0471142727.mb1420s92. View