Literature DB >> 28437075

Fluorescent Photoswitchable Diarylethenes for Biolabeling and Single-Molecule Localization Microscopies with Optical Superresolution.

Benoît Roubinet1, Michael Weber1, Heydar Shojaei1, Mark Bates1, Mariano L Bossi1, Vladimir N Belov1, Masahiro Irie2, Stefan W Hell1.   

Abstract

A modular assembly of water-soluble diarylethenes (DAEs), applicable as biomarkers for optical nanoscopy, is reported. Reversibly photoswitchable 1,2-bis(2-alkyl-6-phenyl-1-benzothiophene-1,1-dioxide-3-yl)perfluorocyclopentenes possessing a fluorescent "closed" form were decorated with one or two methoxy group(s) attached to the para-position(s) of phenyl ring(s) and two, four, or eight carboxylic acid groups. Antibody conjugates of these DAEs feature low aggregation, efficient photoswitching in aqueous buffers, specific staining of cellular structures, and photophysical properties (high emission efficiencies and low cycloreversion quantum yields) enabling their application in superresolution microscopy. Images of tubulin, vimentin, and nuclear pore complexes are presented. The superresolution images can also be acquired by using solely 488 nm light without additional photoactivation with UV light. These DAEs exhibit reversible photoswitching without requiring any additives to the imaging media and open new paths toward the modular design of fluorescent dyes for bioimaging with optical superresolution.

Entities:  

Year:  2017        PMID: 28437075     DOI: 10.1021/jacs.7b00274

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  15 in total

Review 1.  Molecular photoswitches in aqueous environments.

Authors:  Jana Volarić; Wiktor Szymanski; Nadja A Simeth; Ben L Feringa
Journal:  Chem Soc Rev       Date:  2021-11-15       Impact factor: 54.564

2.  De Novo-Designed Near-Infrared Nanoaggregates for Super-Resolution Monitoring of Lysosomes in Cells, in Whole Organoids, and in Vivo.

Authors:  Hongbao Fang; Shankun Yao; Qixin Chen; Chunyan Liu; Yuqi Cai; Shanshan Geng; Yang Bai; Zhiqi Tian; Amanda L Zacharias; Takanori Takebe; Yuncong Chen; Zijian Guo; Weijiang He; Jiajie Diao
Journal:  ACS Nano       Date:  2019-12-09       Impact factor: 15.881

Review 3.  Switchable Fluorophores for Single-Molecule Localization Microscopy.

Authors:  Honglin Li; Joshua C Vaughan
Journal:  Chem Rev       Date:  2018-09-17       Impact factor: 60.622

4.  Quinoline-containing diarylethenes: bridging between turn-on fluorescence, RGB switching and room temperature phosphorescence.

Authors:  Zhen Xu; Qian T Liu; Xiaozhu Wang; Qian Liu; Duane Hean; Keng C Chou; Michael O Wolf
Journal:  Chem Sci       Date:  2020-02-10       Impact factor: 9.825

5.  Turn-off mode fluorescent norbornadiene-based photoswitches.

Authors:  Behabitu Ergette Tebikachew; Fredrik Edhborg; Nina Kann; Bo Albinsson; Kasper Moth-Poulsen
Journal:  Phys Chem Chem Phys       Date:  2018-09-19       Impact factor: 3.676

6.  A building-block design for enhanced visible-light switching of diarylethenes.

Authors:  Zhiwei Zhang; Wenhui Wang; Peipei Jin; Jiadan Xue; Lu Sun; Jinhai Huang; Junji Zhang; He Tian
Journal:  Nat Commun       Date:  2019-09-17       Impact factor: 14.919

7.  Tetrazine as a general phototrigger to turn on fluorophores.

Authors:  Axel Loredo; Juan Tang; Lushun Wang; Kuan-Lin Wu; Zane Peng; Han Xiao
Journal:  Chem Sci       Date:  2020-04-07       Impact factor: 9.825

8.  Photoswitchable Fluorescent Diarylethene Derivatives with Thiophene 1,1-Dioxide Groups: Effect of Alkyl Substituents at the Reactive Carbons.

Authors:  Masakazu Morimoto; Takaki Sumi; Masahiro Irie
Journal:  Materials (Basel)       Date:  2017-09-02       Impact factor: 3.623

9.  Targeted photoswitchable imaging of intracellular glutathione by a photochromic glycosheet sensor.

Authors:  Xianzhi Chai; Hai-Hao Han; Yi Zang; Jia Li; Xiao-Peng He; Junji Zhang; He Tian
Journal:  Beilstein J Org Chem       Date:  2019-10-07       Impact factor: 2.883

10.  Mono- and bithiophene-substituted diarylethene photoswitches with emissive open or closed forms.

Authors:  A Lennart Schleper; Mariano L Bossi; Vladimir N Belov; Stefan W Hell
Journal:  Beilstein J Org Chem       Date:  2019-10-01       Impact factor: 2.883

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