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Updated: Jan 20, 2026

Glutamine Flux Imaging Using Genetically Encoded Sensors
Published on: July 31, 2014
An efficient fluorescence sensor for nitroreductase selective imaging based on intramolecular photoinduced electron
Na Zhang1, Yali Wang1, Shan Leng2
1State Key Laboratory of Bioactive Substances and Function of Natural Medicine, Beijing Key Laboratory of Active Substances Discovery and Drugability Evaluation, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China; School of Life and Environment Sciences, Harbin University of Commerce, Harbin 150076, China.
A new fluorescent sensor rapidly detects nitroreductase (NTR) in bacterial pathogens. This enzyme detection offers a promising tool for diagnosing bacterial infections and guiding antimicrobial selection.
Area of Science:
- Biomedical Engineering
- Chemical Biology
- Medical Diagnostics
Background:
- Bacterial infections pose significant public health challenges, necessitating rapid and accurate diagnostic tools.
- Enzyme-activated fluorogenic probes offer a sensitive approach for detecting bacterial activity.
- Nitroreductase (NTR) is a key enzyme in bacterial metabolism, making it a potential diagnostic target.
Purpose of the Study:
- To develop a novel fluorescent sensor for the selective and sensitive detection of nitroreductase (NTR) activity.
- To demonstrate the probe's utility in visualizing NTR in vitro and in living bacterial pathogens.
- To explore the potential of this sensor for rapid, noninvasive diagnosis of bacterial infections.
Main Methods:
- Design and synthesis of a cyanine fluorophore-based sensor.
- Utilizing photoinduced electron transfer (PET) for fluorescence quenching and activation.
- Catalytic reduction by NTR to trigger a significant fluorescence response.
- In vitro and in vivo imaging of NTR activity in bacterial pathogens.
Main Results:
- The developed sensor exhibited a rapid, 10-fold increase in fluorescence upon catalytic reduction by NTR.
- High selectivity and sensitivity were achieved for NTR detection.
- Successful visualization of NTR activity in both cell-free systems and live bacterial pathogens.
- The probe demonstrated potential for distinguishing between bacterial types based on NTR activity.
Conclusions:
- A novel, enzyme-activated fluorescent probe for NTR detection has been successfully developed.
- The probe enables rapid, selective, and sensitive visualization of NTR activity in bacterial pathogens.
- This technology holds significant promise for noninvasive diagnosis of bacterial infections and guiding antimicrobial therapy.
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