2015
DOI: 10.1021/acs.analchem.5b01657
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Enzymatic Hydrogelation-Induced Fluorescence Turn-Off for Sensing Alkaline Phosphatase in Vitro and in Living Cells

Abstract: Alkaline phosphatase (ALP)-catalyzed hydrogelation has been extensively explored and found wide applications. Spectroscopic and electrochemical approaches are commonly employed for the detection of ALP activity. Herein, by rational design of a fluorescence probe Fmoc-K(FITC)FFYp (P1) (where FITC is fluorescein), we incorporated sol-gel transition with fluorescence "turn-off" and developed a new method for quantitative sensing ALP activity in vitro and in living cells. Under the catalysis of ALP, P1 was convert… Show more

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Cited by 140 publications
(70 citation statements)
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“…Enhanced quenching has been employed by researchers to detect the activity of enzymes (ex. caspase 3 [79], alkaline phosphatase [80], etc.). However, self-assembly can also leads to a reduction of the charge transfer between the fluorophore and the polar solvent, and thus an increment of fluorescence [81].…”
Section: Peptide-peptide Interaction Driven Self-assemblymentioning
confidence: 99%
“…Enhanced quenching has been employed by researchers to detect the activity of enzymes (ex. caspase 3 [79], alkaline phosphatase [80], etc.). However, self-assembly can also leads to a reduction of the charge transfer between the fluorophore and the polar solvent, and thus an increment of fluorescence [81].…”
Section: Peptide-peptide Interaction Driven Self-assemblymentioning
confidence: 99%
“…Among these assays, fluorometric methods have attracted considerable interest for their rapid response, easy operation and high sensitivity 1719 . Traditional fluorescent methods are mainly based on organic dyes 20, 21 , fluorescent polymers 22, 23 and metal nanoclusters or nanoparticles 2426 . Whereas, most of them have poor photostability, laborious synthetic procedures, and complexed labeling processes.…”
Section: Introductionmentioning
confidence: 99%
“…Higher and lower activities of ALP are utilized as am arker for liver,b one, and hypophosphatasia-relatedd isorders. [83,84] Pyrophosphate (PPi)i sa natural substrate that inhibits the fluorescencea ctivity of dsDNA-templated CuNPs by forming ac omplex with Cu 2 + and terminating the growth of CuNPs.A LP hydrolyzes PPi into inorganic phosphate (Pi), which cannot form ac omplex with Cu 2 + .T he resultant fluorescencei ntensity of dsDNA-templated CuNPsr emains, as shown in Figure 4A.…”
Section: Copper Nps As Af Luorescencebiosensormentioning
confidence: 99%