4.6 Article

Rational design of a HA-AuNPs@AIED nanoassembly for activatable fluorescence detection of HAase and imaging in tumor cells

Journal

ANALYTICAL METHODS
Volume 13, Issue 17, Pages 2030-2036

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0ay02130j

Keywords

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Funding

  1. NSFC [51873058, 21705040, 51773056]
  2. Hunan Provincial Natural Science Foundation of China [2020JJ3021, 2018JJ3143]
  3. China Postdoctoral Science Foundation [2018T110824]
  4. Scientific Research Fund of Hunan Provincial Education Department [19B204]
  5. Open Project Program of the State Key Laboratory of Chemo/Biosensing and Chemometrics [2018011]
  6. Open Fund of the State Key Laboratory of Luminescent Materials and Devices (South China University of Technology) [2019-skllmd-09]
  7. Shandong Key Laboratory of Biochemical Analysis

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A novel AIE-dot-based nanoprobe was proposed for hyaluronidase detection, exhibiting high sensitivity, excellent selectivity, and anti-interference capabilities. The nanoprobe offers a practicable turn-on strategy for specific fluorescence imaging of HAase in live tumor cells, showing promise for recognition and imaging of HAase in tumors in biological research.
Aggregation induced emission (AIE) dots have gained broad attention in fluorescence bioimaging and biosensors in virtue of their distinctive optical properties of splendid biocompatibility, high brightness and good photostability. However, the application of AIE dots in sensing and imaging of enzymes in cells remains at an early stage and needs to be further explored. In this report, we proposed a novel AIE-dot-based nanoprobe for hyaluronidase (HAase) detection using a simple electrostatic self-assembly of AIE dots with gold nanoparticles functionalized using hyaluronic acid (HA-AuNPs), named HA-AuNPs@AIEDs. The fluorescence of AIE dots can be obviously quenched by HA-AuNPs via fluorescence resonance energy transfer (FRET). HAase could degrade HA into small pieces and thus induce disassembly of AuNPs and AIEDs, accompanied by fluorescence recovery of AIEDs. The as-prepared nanoprobe exhibited high sensitivity, excellent selectivity, wide response range and desirable anti-interference for quantitative sensing of HAase in vitro. The detection limit was down to 0.0072 U mL(-1). Moreover, the nanoprobe displayed good biocompatibility and excellent photostability, and thus offered a practicable turn-on strategy for specific, high-contrast fluorescence imaging of HAase in live tumor cells. The AIE-based nanoprobe may provide a novel universal platform for recognition and imaging of HAase in tumors, and may be beneficial for related biological research.

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