2019
DOI: 10.1039/c9nj03375k
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A FRET-based ratiometric fluorescent probe for highly selective detection of cysteine based on a coumarin–rhodol derivative

Abstract: A ratiometric fluorescent probe for detecting cysteine was designed and synthesized based on the fluorescence resonance energy transfer (FRET) process.

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Cited by 26 publications
(22 citation statements)
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“…FRET sensors that use l -(7-hydroxycoumarin-4-yl)ethylglycine, an unnatural fluorescent amino acid, for glutamine and methionine have also been reported [ 323 , 324 ]. Beyond genetically encoded sensors, two irreversible FRET-based synthetic probes selective for cysteine with applications in mammalian cells are also recently available (Table 2) [ 325 , 326 ].…”
Section: Fluorescence Imagingmentioning
confidence: 99%
“…FRET sensors that use l -(7-hydroxycoumarin-4-yl)ethylglycine, an unnatural fluorescent amino acid, for glutamine and methionine have also been reported [ 323 , 324 ]. Beyond genetically encoded sensors, two irreversible FRET-based synthetic probes selective for cysteine with applications in mammalian cells are also recently available (Table 2) [ 325 , 326 ].…”
Section: Fluorescence Imagingmentioning
confidence: 99%
“…The linear regression equation was F = 63.5503 + 223.0080 × 10 6 × C ( r = 0.9988), where F denotes the measured fluorescence intensity, C represents the concentration of HOCl, and r is the linear correlation coefficient. The detection limit was calculated by three times standard deviation of blank solution [ 48 , 49 ]. The detection limit was found to be 1.5 × 10 −7 mol·L −1 for the fluorescent probe.…”
Section: Resultsmentioning
confidence: 99%
“…0.4 g of 2 (1.8 mmol) and 0.3 g of 4 (1 mmol) were added to a 100 mL roundbottomed flask containing 20 mL of absolute ethanol and 0.5 mL of piperidine; the reaction mixture was stirred at 80 °C for 4 h under N 2 protection, and then, the mixture was subjected to rotary evaporation and purified by column chromatography (DCM/MeOH/HAc = 100:1:1, v/v/v) to afford KQ−SO 2 as a purple solid with a yield of 80%. 1 H NMR (400 MHz, DMSO-d 6 ): 9.14 (s, 1H), 8.68−8.64 (d, J = 16.0 Hz, 1H), 8.41−8.39 (d, J = 8.0 Hz, 1H), 8.28−8.26 (d, J = 8.0 Hz, 1H), 7.89−7.85 (dd, J 1 = 8.0 Hz, J 2 = 4.0 Hz, 3H), 7.74−7.61 (t, J = 26.0 Hz, 2H), 7.61−7.57 (m, 3H), 7.40−7.36 (t, J = 8.0 Hz, 1H), 4.59−4.54 (dd, J 1 = 8.0 Hz, J 2 = 4.0 Hz, 2H), 4.17 (s, 3H), 1.65 (s, 6H), 1.40−1.36 (t, J = 8.0 Hz, 3H); 13 Spectrophotometric Measurements. Fluorescence measurement experiments were measured in 10 mM phosphate buffer solution with DMSO as cosolvent solution (H 2 O/DMSO = 99:1, v/v).…”
Section: ■ Materials and Methodsmentioning
confidence: 99%
“…In recent years, the fluorescence detection imaging technology has shown many advantages, such as real-time detection, simple operation, less damage to the object under test, high sensitivity, and high selectivity, and has attracted more and more attention from scientific researchers. Until now, many fluorescent sensors for detecting SO 2 were developed, which is based on nucleophilic addition reactions with the electron-deficit “CC”, ketone, or aldehyde groups and inhibition of CN isomerization. However, there are also many challenges for rapid and highly selective detection in real samples and biological systems.…”
Section: Introductionmentioning
confidence: 99%