Development of a near-infrared fluorescent probe for imaging of endogenous Cu+ in live cells

2012 ◽  
Vol 48 (50) ◽  
pp. 6247 ◽  
Author(s):  
Xiaowei Cao ◽  
Weiying Lin ◽  
Wei Wan
2020 ◽  
Vol 36 (9) ◽  
pp. 1053-1057
Author(s):  
Yuhui MEN ◽  
Xiaomin ZHOU ◽  
Zhijie YAN ◽  
Linqiang NIU ◽  
Yang LUO ◽  
...  

2016 ◽  
Vol 12 (4) ◽  
pp. 1114-1117 ◽  
Author(s):  
Sandra G. König ◽  
Simin Öz ◽  
Roland Krämer

We describe a NIR-fluorescent marker which is efficiently internalized by live cells in the presence exogenous zinc(II) whereas only negligible staining was detected in the absence of zinc(II).


2016 ◽  
Vol 236 ◽  
pp. 268-275 ◽  
Author(s):  
Fan Wu ◽  
Chaoxing Liu ◽  
Yuqi Chen ◽  
Shixi Yang ◽  
Jiahui Xu ◽  
...  

2019 ◽  
Vol 17 (26) ◽  
pp. 6398-6403 ◽  
Author(s):  
Tong Chen ◽  
Zikang Chen ◽  
Ruiyuan Liu ◽  
Shaobing Zheng

A D–π-A structure near-infrared fluorescent probe (Lyso-BTC) is explored for its fluorescence visualization and detection of lysosomes in view of a large Stokes shift (∼190 nm), NIR emission (685 nm), excellent photostability, fluorescence response to viscosity, and lysosome-targeted property.


2021 ◽  
Vol 57 (22) ◽  
pp. 2800-2803
Author(s):  
Jinye Niu ◽  
Yong Li ◽  
Ran Zhang ◽  
Jian Zhang ◽  
Xu Wang ◽  
...  

Based on the thiolysis of dinitrophenyl ethers, a nucleus-targeted fluorescent probe, AQD, with bisalkylaminoanthraquinone as the fluorophore, was prepared for the near-infrared mapping of thiophenol in live cells, zebrafish, and mice.


2016 ◽  
Vol 43 (5) ◽  
pp. 2945-2957 ◽  
Author(s):  
Yichen Jiang ◽  
Di Jin ◽  
Yang Li ◽  
Xilong Yan ◽  
Ligong Chen

2019 ◽  
Vol 171 ◽  
pp. 107698 ◽  
Author(s):  
Guimei Wang ◽  
Xiaoxue Jiang ◽  
Nanyan Fu

Molecules ◽  
2020 ◽  
Vol 25 (3) ◽  
pp. 437 ◽  
Author(s):  
Ismail Ismail ◽  
Zhuoyue Chen ◽  
Xiuru Ji ◽  
Lu Sun ◽  
Long Yi ◽  
...  

Near-infrared (NIR) fluorescent probes are attractive tools for bioimaging applications because of their low auto-fluorescence interference, minimal damage to living samples, and deep tissue penetration. H2S is a gaseous signaling molecule that is involved in redox homeostasis and numerous biological processes in vivo. To this end, we have developed a new red shifted fluorescent probe 1 to detect physiological H2S in live cells. The probe 1 is based on a rhodamine derivative as the red shifted fluorophore and the thiolysis of 7-nitro 1,2,3-benzoxadiazole (NBD) amine as the H2S receptor. The probe 1 displays fast fluorescent enhancement at 660 nm (about 10-fold turn-ons, k2 = 29.8 M−1s−1) after reacting with H2S in buffer (pH 7.4), and the fluorescence quantum yield of the activated red shifted product can reach 0.29. The probe 1 also exhibits high selectivity and sensitivity towards H2S. Moreover, 1 is cell-membrane-permeable and mitochondria-targeting, and can be used for imaging of endogenous H2S in living cells. We believe that this red shifted fluorescent probe can be a useful tool for studies of H2S biology.


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