Literature DB >> 24377865

Recent advances in super-resolution fluorescence imaging and its applications in biology.

Rongcheng Han1, Zhenghong Li2, Yanyan Fan2, Yuqiang Jiang3.   

Abstract

Fluorescence microscopy has become an essential tool for biological research because it can be minimally invasive, acquire data rapidly, and target molecules of interest with specific labeling strategies. However, the diffraction-limited spatial resolution, which is classically limited to about 200 nm in the lateral direction and about 500 nm in the axial direction, hampers its application to identify delicate details of subcellular structure. Extensive efforts have been made to break diffraction limit for obtaining high-resolution imaging of a biological specimen. Various methods capable of obtaining super-resolution images with a resolution of tens of nanometers are currently available. These super-resolution techniques can be generally divided into three primary classes: (1) patterned illumination-based super-resolution imaging, which employs spatially and temporally modulated illumination light to reconstruct sub-diffraction structures; (2) single-molecule localization-based super-resolution imaging, which localizes the profile center of each individual fluorophore at subdiffraction precision; (3) bleaching/blinking-based super-resolution imaging. These super-resolution techniques have been utilized in different biological fields and provide novel insights into several new aspects of life science. Given unique technical merits and commercial availability of super-resolution fluorescence microscope, increasing applications of this powerful technique in life science can be expected.
Copyright © 2013. Published by Elsevier Ltd.

Keywords:  Bio-imaging; FPALM; Fluorescence microscopy; NSOM; Optical diffraction limit; PALM; RESOLFT; SSIM; STED; STORM; Super-resolution; TIRF; fluorescence photoactivation localization microscopy; near-field scanning optical microscopy; photoactivated localization microscopy; reversible saturable optically linear fluorescence transitions; saturated structured-illumination microscopy; stimulated emission depletion; stochastic optical reconstruction microscopy; total internal reflection fluorescence microscopy

Mesh:

Year:  2013        PMID: 24377865     DOI: 10.1016/j.jgg.2013.11.003

Source DB:  PubMed          Journal:  J Genet Genomics        ISSN: 1673-8527            Impact factor:   4.275


  12 in total

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4.  BiP clustering facilitates protein folding in the endoplasmic reticulum.

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8.  LSPR-mediated high axial-resolution fluorescence imaging on a silver nanoparticle sheet.

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9.  Super-Resolution Microscopy in Studying the Structure and Function of the Cell Nucleus.

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Journal:  Acta Naturae       Date:  2017 Oct-Dec       Impact factor: 1.845

10.  Real-time visualization of clustering and intracellular transport of gold nanoparticles by correlative imaging.

Authors:  Mengmeng Liu; Qian Li; Le Liang; Jiang Li; Kun Wang; Jiajun Li; Min Lv; Nan Chen; Haiyun Song; Joon Lee; Jiye Shi; Lihua Wang; Ratnesh Lal; Chunhai Fan
Journal:  Nat Commun       Date:  2017-05-31       Impact factor: 14.919

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