A Turn‐On Fluorescence Probe for Rapid Detection of Hypochlorite in Living Cells and in Vitro

2019 ◽  
Vol 4 (27) ◽  
pp. 8021-8025 ◽  
Author(s):  
Ya Xie ◽  
Lijia Haung ◽  
Liqiang Yan ◽  
Jianping Li
2016 ◽  
Vol 237 ◽  
pp. 501-508 ◽  
Author(s):  
Yaming Liu ◽  
Jinyu Zhang ◽  
Jiaxi Ru ◽  
Xiang Yao ◽  
Yang Yang ◽  
...  

2018 ◽  
Author(s):  
Nidhi Gour ◽  
Vivek Shinh Kshtriya ◽  
Bharti Koshti ◽  
Shradhey Gupta ◽  
khashti Ballabh Joshi ◽  
...  

<p>We report efficient synthesis and photophysical properties of a novel fluorescent pyridothiazole based construct by a facile methodology and its application as a sensor for rapid, selective as well as sensitive detection of amyloid fibres. The novel compound has exceptionally high quantum yield and sensitivity. The fluorescence of pyridothiazole construct is completely quenched (Turn-OFF) upon addition of cupric ions and the fluorescence is recovered on addition of amyloidogenic peptides like A<i>β</i><sub>42 </sub>(Turn-ON). The control experiment with native and heat treated BSA suggest that the new probe binds to beeta/<i>β</i> sheets present in amyloid. The new probe offers direct visualization of fluorescence ‘Turn-OFF’ ‘Turn-ON’ under long UV without the use of sophisticated instrumentation. Hence, a very simple, facile and cost-effective methodology for the rapid detection of amyloid is presented and it may in all possibility pave the way for the design of a better probe for sensing amyloids than conventional ThT.</p>


The Analyst ◽  
2016 ◽  
Vol 141 (8) ◽  
pp. 2600-2605 ◽  
Author(s):  
Xiaomei Liu ◽  
Shuang Liu ◽  
Gaolin Liang

A water-soluble, biocompatible, small molecular fluorescent turn-on probe was developed for the highly selective and sensitive detection of NO in vitro and in living cells.


2015 ◽  
Vol 7 (18) ◽  
pp. 7534-7539 ◽  
Author(s):  
Dehuan Yu ◽  
Qisong Zhai ◽  
Shengjun Yang ◽  
Guoqiang Feng

A colorimetric and NIR fluorescent turn-on probe was reported for rapid detection of thiophenols.


2021 ◽  
Author(s):  
Masayori Hagimori ◽  
Yasushi Karimine ◽  
Naoko Mizuyama ◽  
Fumiko Hara ◽  
Takeshi Fujino ◽  
...  

Abstract Fluorescence probes that selectively image cadmium are useful for detecting and tracking the amount of Cd2+ in cells and tissues. In this study, we designed and synthesized a novel Cd2+ fluorescence probe based on the pyridine-pyrimidine structure, 4-(methylsulfanyl)-6-(pyridin-2-yl)pyrimidin-2-amine (3), as a low-molecular-weight fluorescence probe for Cd2+. Compound 3 could successfully discriminate between Cd2+ and Zn2+ and exhibited a highly selective turn-on response toward Cd2+ over biologically related metal ions. The dissociation constant and detection limit of 5.4 x 10− 6 mol L− 1 and 4.4 × 10− 7 mol L− 1, respectively, were calculated using fluorescence titration experiments. Studies with closely related analogs showed that the bis-heterocyclic moiety of 3 acted as both a coordination site for Cd2+ and a fluorophore. Further, the methylsulfanyl group of compound 3 is essential for achieving selective and sensitive Cd2+ detection. Fluorescence microscopy studies using living cells revealed that the cell membrane permeability of compound 3 is sufficient to detect intracellular Cd2+. These results indicate that novel bis-heterocyclic molecule 3 has considerable potential as a fluorescence probe for Cd2+ in biological applications.


2018 ◽  
Vol 42 (11) ◽  
pp. 8325-8329 ◽  
Author(s):  
An Xu ◽  
Yonghe Tang ◽  
Weiying Lin

The first mitochondrial-targeted two-photon fluorescence probe (MT-FA) for formaldehyde (FA) was engineered for monitoring FA in the mitochondria of living cells and liver tissues in one- and two-photon modes.


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