2021
DOI: 10.1016/j.bmcl.2021.128049
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A bioluminescent probe for in vivo imaging of pyroglutamate aminopeptidase in a mouse model of inflammation

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Cited by 9 publications
(8 citation statements)
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“…[109,110] Hu et al used the firefly luciferase system to develop a probe PBL that constructed by coupling D-aminofluorescein with pyroglutamate via an amide bond, which can be considered as a dipeptide derivative and can be used to detect PGP in vitro and in vivo (Figure 6). [111] In vivo imaging of a mouse model of symptomatic liver disease demonstrated excellent sensitivity and selectivity of the probe. The probe provided a powerful tool for studying the physiological and pathological processes of PGP, which allowed the detection of PGP activity in living animals of various pathological conditions and normal physiological processes including inflammation.…”
Section: Detection Of Inflammationmentioning
confidence: 98%
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“…[109,110] Hu et al used the firefly luciferase system to develop a probe PBL that constructed by coupling D-aminofluorescein with pyroglutamate via an amide bond, which can be considered as a dipeptide derivative and can be used to detect PGP in vitro and in vivo (Figure 6). [111] In vivo imaging of a mouse model of symptomatic liver disease demonstrated excellent sensitivity and selectivity of the probe. The probe provided a powerful tool for studying the physiological and pathological processes of PGP, which allowed the detection of PGP activity in living animals of various pathological conditions and normal physiological processes including inflammation.…”
Section: Detection Of Inflammationmentioning
confidence: 98%
“…Reproduced with permission. [111] Copyright 2013, Elsevier. which provided a guarantee for solving the problems of disease detection.…”
Section: Detection Of Inflammationmentioning
confidence: 99%
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“…22 Moreover, the intrinsic drawbacks of fluorescence imaging, including photobleaching, autofluorescence, and light scattering, restrict its applicability as a method for in vivo biological detection and imaging. 23,24 Therefore, it is still necessary to develop more efficient and novel strategies for the in vitro and in vivo monitoring of CES2.…”
Section: Introductionmentioning
confidence: 99%
“…In addition to fluorescence, bioluminescence generated by luciferase-catalyzed oxidation of chemical substrates is an alternative for analytes detection in complex samples. , In comparison with fluorescence probes, the bioluminescent probes cause negligible background autofluorescence due to the elimination of external optical excitation, providing high signal-to-noise ratio and sensitivity in detection. Previous bioluminescent probes usually cage the bioluminescent substrates, such as luciferin and coelenterazine, with specific recognition units to form a prosubstrate, which can be oxidized by luciferase after reaction with targets. , Based on this strategy, many bioluminescent probes have achieved gratifying results in in vitro visual detection, bioimaging of diseases biomarkers, such as enzymes, metal ions, , reactive oxygen species (ROS), and reactive sulfide species (RSS). However, the signal intensity of the turn-on bioluminescent probes decays sharply with the consumption of substrate, which severely hinders their quantitative analysis in practical applications.…”
Section: Introductionmentioning
confidence: 99%