Literature DB >> 26743847

Where Do We Stand with Super-Resolution Optical Microscopy?

Karin Nienhaus1, G Ulrich Nienhaus2.   

Abstract

Super-resolution fluorescence microscopy has become an invaluable, powerful approach to study biomolecular dynamics and interactions via selective labeling and observation of specific molecules in living cells, tissues and even entire organisms. In this perspective, we present a brief overview of the main techniques and their application to cellular biophysics. We place special emphasis on super-resolution imaging via single-molecule localization microscopy and stimulated emission depletion/reversible saturable optical fluorescence transitions microscopy, and we also briefly address fluorescence fluctuation approaches, notably raster image correlation spectroscopy, as tools to record fast diffusion and transport.
Copyright © 2016 Elsevier Ltd. All rights reserved.

Keywords:  fluorescence correlation spectroscopy; localization microscopy; raster image correlation spectroscopy; stimulated emission depletion microscopy; super-resolution fluorescence microscopy

Mesh:

Substances:

Year:  2015        PMID: 26743847     DOI: 10.1016/j.jmb.2015.12.020

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  15 in total

1.  High-numerical-aperture cryogenic light microscopy for increased precision of superresolution reconstructions.

Authors:  Marc Nahmani; Conor Lanahan; David DeRosier; Gina G Turrigiano
Journal:  Proc Natl Acad Sci U S A       Date:  2017-03-27       Impact factor: 11.205

2.  Development of nanoscale structure in LAT-based signaling complexes.

Authors:  Valarie A Barr; Eilon Sherman; Jason Yi; Itoro Akpan; Alexandre K Rouquette-Jazdanian; Lawrence E Samelson
Journal:  J Cell Sci       Date:  2016-11-10       Impact factor: 5.285

3.  Extraction of Hidden Science from Nanoscale Images.

Authors:  Kristopher B Barr; Naihao Chiang; Andrea L Bertozzi; Jérôme Gilles; Stanley J Osher; Paul S Weiss
Journal:  J Phys Chem C Nanomater Interfaces       Date:  2021-12-23       Impact factor: 4.177

Review 4.  Using single-vesicle technologies to unravel the heterogeneity of extracellular vesicles.

Authors:  Guillermo Bordanaba-Florit; Félix Royo; Sergei G Kruglik; Juan M Falcón-Pérez
Journal:  Nat Protoc       Date:  2021-06-16       Impact factor: 13.491

5.  Confocal and Super-resolution Imaging of RNA in Live Bacteria Using a Fluorogenic Silicon Rhodamine-binding Aptamer.

Authors:  Regina Wirth; Peng Gao; G Ulrich Nienhaus; Murat Sunbul; Andres Jäschke
Journal:  Bio Protoc       Date:  2020-05-05

6.  Stochastic optical reconstruction microscopy-based relative localization analysis (STORM-RLA) for quantitative nanoscale assessment of spatial protein organization.

Authors:  Rengasayee Veeraraghavan; Robert G Gourdie
Journal:  Mol Biol Cell       Date:  2016-06-15       Impact factor: 4.138

7.  Accelerated super-resolution imaging with FRET-PAINT.

Authors:  Jongjin Lee; Sangjun Park; Wooyoung Kang; Sungchul Hohng
Journal:  Mol Brain       Date:  2017-12-28       Impact factor: 4.041

Review 8.  Deciphering Structural Photophysics of Fluorescent Proteins by Kinetic Crystallography.

Authors:  Dominique Bourgeois
Journal:  Int J Mol Sci       Date:  2017-06-02       Impact factor: 5.923

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

Authors:  S S Ryabichko; A N Ibragimov; L A Lebedeva; E N Kozlov; Y V Shidlovskii
Journal:  Acta Naturae       Date:  2017 Oct-Dec       Impact factor: 1.845

10.  Super-resolution microscopy reveals functional organization of dopamine transporters into cholesterol and neuronal activity-dependent nanodomains.

Authors:  Troels Rahbek-Clemmensen; Matthew D Lycas; Simon Erlendsson; Jacob Eriksen; Mia Apuschkin; Frederik Vilhardt; Trine N Jørgensen; Freja H Hansen; Ulrik Gether
Journal:  Nat Commun       Date:  2017-09-29       Impact factor: 14.919

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