4.7 Article

Coumarin-based turn-on fluorescence probe with a large Stokes shift for detection of endogenous neutrophil elastase in live cells and zebrafish

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.saa.2022.121563

Keywords

Coumarin; Fluorescence probe; Neutrophil elastase; Large Stokes shift; Bioimaging

Categories

Funding

  1. National Natural Science Foundation of China [21804102]
  2. Hubei key Laboratory of Novel Reactor and Green Chemistry Technology of Wuhan Institute of Technology [NRG202107]
  3. Special Projects of the Central Government in Guidance of Local Science and Technology Development in Hubei Province [2020ZYYD040]
  4. second batch of the Key Research and Development Project of Hubei Province [2020BAB073]
  5. Open Project of Key Laboratory of Novel Biomass-Based Environmental and Energy Materials in Petroleum and Chemical Industry [BEEA0001]
  6. Outstanding Young and Middle-aged Scientific Innovation Team of Colleges and Universities of Hubei Province [T201908]
  7. Graduate Innovative Fund of Wuhan Institute of Technology [CX2021360]

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Researchers have designed a novel fluorescent probe HNCOU-NE for visualizing NE activity in living cells and zebrafish, which can be used for qualitative and quantitative detection of NE activity in vitro and in vivo.
Neutrophil elastase (NE), a serine proteinase, is a significant biomarker which is closely related to the progress of diseases. However, only few probes have been reported for detection of NE activity and cell imaging. And these probes have exhibited small Stokes shift, which leads to high fluorescence interferences. Furthermore, only one probe among them is able to image NE in vivo successfully. To overcome the above problems, we designed a novel coumarin-based fluorescent probe HNCOU-NE with large Stokes shift to visualize NE activity in living cells and zebrafish. The new probe HNCOU-NE for NE contains fluorophore HNCOU as the reporter and pentafluoroethyl as the enzyme-active trigger moiety. As expected, HNCOU-NE displays perfect detecting performance for sensing of NE, including good water solubility, large Stokes shift, high affinity and wide linear response concentration. In addition, HNCOU-NE has been successfully utilized for NE real-time detection and imaging in different living cells, exhibiting low cytotoxicity and excellent biocompatibility. Most importantly, endogenous NE fluorescence imaging experiments reveals that HNCOU-NE can distinguish liver cancer cells (HepG2) and other cells (293T, HeLa and SKOV3), illustrating its specific ability to diagnose liver cancer cells. Besides, probe HNCOU-NE also has the ability to specifically detect endogenous NE activity in living zebrafish. All the results indicate that HNCOU-NE is a valuable probe for qualitative and quantitative sensing of NE activity in vitro and in vivo.

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