scholarly journals Hydroxylated Fluorescent Dyes for Live-Cell Labeling: Synthesis, Spectra and Super-Resolution STED

2017 ◽  
Vol 23 (50) ◽  
pp. 12114-12119 ◽  
Author(s):  
Alexey N. Butkevich ◽  
Vladimir N. Belov ◽  
Kirill Kolmakov ◽  
Viktor V. Sokolov ◽  
Heydar Shojaei ◽  
...  
2019 ◽  
Author(s):  
Inbar Segal ◽  
Dikla Nachmias ◽  
Eyal Arbely ◽  
Natalie Elia

AbstractIn the high-resolution microscopy era, genetic code expansion (GCE)-based bioorthogonal labeling offers an elegant way for direct labeling of proteins in live cells with fluorescent dyes. This labeling approach is currently not broadly used live cell applications, partly because it needs to be adjusted to the specific protein under study. Here, we present a generic, 14-residues long, N-terminal tag for GCE-based labeling of proteins in live mammalian cells. Using this tag, we generated a library of GCE-based organelle markers, demonstrating the applicability of the tag for labeling a plethora of proteins and organelles. Finally, we show that the HA epitope, used as a backbone in our tag, can be substituted with other epitopes and, in some cases, can be completely removed, reducing the tag length to 5 residues. The GCE-tag presented here offers a powerful, easy-to-implement tool for live cell labeling of cellular proteins with small and bright probes.


2014 ◽  
Vol 53 (8) ◽  
pp. 2245-2249 ◽  
Author(s):  
Ivana Nikić ◽  
Tilman Plass ◽  
Oliver Schraidt ◽  
Jędrzej Szymański ◽  
John A. G. Briggs ◽  
...  

2021 ◽  
Vol 8 ◽  
Author(s):  
Yubing Han ◽  
Zhimin Zhang ◽  
Wenjie Liu ◽  
Yuanfa Yao ◽  
Yingke Xu ◽  
...  

Despite the urgent need to image living specimens for cutting-edge biological research, most existing fluorescent labeling methods suffer from either poor optical properties or complicated operations required to realize cell-permeability and specificity. In this study, we introduce a method to overcome these limits—taking advantage of the intrinsic affinity of bright and photostable fluorophores, no matter if they are supposed to be live-cell incompatible or not. Incubated with living cells and tissues in particular conditions (concentration and temperature), some Atto and BODIPY dyes show live-cell labeling capability for specific organelles without physical cell-penetration or chemical modifications. Notably, by using Atto 647N as a live-cell mitochondrial marker, we obtain 2.5-time enhancement of brightness and photostability compared with the most commonly used SiR dye in long-term imaging. Our strategy has expanded the scientist's toolbox for understanding the dynamics and interactions of subcellular structures in living specimens.


2020 ◽  
Vol 9 (1) ◽  
Author(s):  
Gerti Beliu ◽  
Markus Sauer

AbstractNew peptide vehicles enable the efficient live-cell labeling of intracellular organelles with cell-impermeable fluorescent probes by simple coincubation, paving the way for refined multicolor super-resolution fluorescence imaging.


2015 ◽  
Vol 21 (35) ◽  
pp. n/a-n/a
Author(s):  
Jan-Erik Hoffmann ◽  
Tilman Plass ◽  
Ivana Nikić ◽  
Iker Valle Aramburu ◽  
Christine Koehler ◽  
...  

PLoS ONE ◽  
2015 ◽  
Vol 10 (11) ◽  
pp. e0141918 ◽  
Author(s):  
Zhongqiu Ni ◽  
Lanxia Zhou ◽  
Xu Li ◽  
Jing Zhang ◽  
Shouliang Dong

2020 ◽  
Vol 2 (12) ◽  
pp. 5803-5809
Author(s):  
Lei Dong ◽  
Dehong Hu ◽  
Yanding Wang ◽  
Zonghai Sheng ◽  
Mei Hong ◽  
...  

The smallest-pore SAPO-20 zeolite confined pyrolysis of organics afforded ultrasmall uniform carbon dots with excellent performance in bioimaging.


2004 ◽  
Vol 16 (12) ◽  
pp. 961-966 ◽  
Author(s):  
A. M. Derfus ◽  
W. C. W. Chan ◽  
S. N. Bhatia

2010 ◽  
Vol 59 (3) ◽  
pp. 357-363 ◽  
Author(s):  
Ophélie Nicolle ◽  
Astrid Rouillon ◽  
Helene Guyodo ◽  
Zohreh Tamanai-Shacoori ◽  
Fatiha Chandad ◽  
...  

ChemMedChem ◽  
2017 ◽  
Vol 12 (23) ◽  
pp. 2006-2013 ◽  
Author(s):  
Yuki Sakai ◽  
Satoshi Mizuta ◽  
Asuka Kumagai ◽  
Mohammed S. O. Tagod ◽  
Hiroaki Senju ◽  
...  

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