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Covalent organic framework-based fluorescent nanoprobe for intracellular pH sensing and imaging
Yutao Jia1, Yanting Shen2, Yanyan Zhu3
1School of Pharmacy, Key Laboratory of Innovative Drug Development and Evaluation, Hebei Medical University, Shijiazhuang 050017, People's Republic of China; College of Chemical Technology, Shijiazhuang University, Shijiazhuang 050035, People's Republic of China.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy
|February 15, 2022
Summary
A new fluorescent probe, methoxy-based covalent organic framework (TAPB-DMTP-COF), enables precise monitoring of lysosomal pH. This tool aids in understanding lysosomal dysfunction and related diseases.
Area of Science:
- Biochemistry
- Materials Science
- Cell Biology
Background:
- Lysosomes are vital acidic organelles involved in cellular degradation.
- Lysosomal pH disturbances are linked to dysfunction and disease.
- Accurate intracellular pH monitoring is crucial for disease research.
Purpose of the Study:
- To develop a novel pH-responsive fluorescent probe for lysosomal pH imaging.
- To investigate the potential of covalent organic frameworks (COFs) for biological sensing.
- To establish a tool for in situ monitoring of lysosomal pH fluctuations.
Main Methods:
- Synthesis of a methoxy-based covalent organic framework (TAPB-DMTP-COF).
- Characterization of the COF's structure, toxicity, and pH responsiveness.
- Utilizing confocal fluorescence imaging for lysosomal pH monitoring in cells.
Main Results:
- The TAPB-DMTP-COF exhibited a regular crystal structure, low toxicity, and good pH responsiveness.
- The probe demonstrated pH-dependent fluorescence with good linearity in aqueous solutions.
- Effective in situ monitoring of lysosomal pH changes (pH 4.0–7.4) was achieved.
Conclusions:
- The developed TAPB-DMTP-COF serves as a selective and effective probe for lysosomal pH imaging.
- This probe offers a new approach for intracellular pH sensing and studying lysosome-related diseases.
- The findings contribute to understanding disease mechanisms linked to abnormal lysosomal pH.

