Volume 134, Issue 14 e202116457
Forschungsartikel

Selective Fluorescence Imaging of Cancer Cells Based on ROS-Triggered Intracellular Cross-Linking of Artificial Enzyme

Yufei Di

Yufei Di

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190 P. R. China

College of Chemistry, University of Chinese Academy of Sciences, Beijing, 100049 P. R. China

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Endong Zhang

Endong Zhang

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190 P. R. China

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Zhiwen Yang

Zhiwen Yang

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190 P. R. China

College of Chemistry, University of Chinese Academy of Sciences, Beijing, 100049 P. R. China

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Qi Shen

Qi Shen

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190 P. R. China

College of Chemistry, University of Chinese Academy of Sciences, Beijing, 100049 P. R. China

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Dr. Xuancheng Fu

Dr. Xuancheng Fu

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190 P. R. China

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Gang Song

Gang Song

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190 P. R. China

College of Chemistry, University of Chinese Academy of Sciences, Beijing, 100049 P. R. China

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Chuanwei Zhu

Chuanwei Zhu

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190 P. R. China

College of Chemistry, University of Chinese Academy of Sciences, Beijing, 100049 P. R. China

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Prof. Haotian Bai

Prof. Haotian Bai

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190 P. R. China

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Prof. Yiming Huang

Corresponding Author

Prof. Yiming Huang

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190 P. R. China

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Prof. Fengting Lv

Prof. Fengting Lv

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190 P. R. China

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Prof. Libing Liu

Prof. Libing Liu

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190 P. R. China

College of Chemistry, University of Chinese Academy of Sciences, Beijing, 100049 P. R. China

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Prof. Shu Wang

Corresponding Author

Prof. Shu Wang

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190 P. R. China

College of Chemistry, University of Chinese Academy of Sciences, Beijing, 100049 P. R. China

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First published: 22 January 2022
Citations: 1

Abstract

Inside living cells, regulation of catalytic activity of artificial enzymes remains challenging due to issues such as biocompatibility, efficiency, and stability of the catalyst, by which the practical applications of artificial enzymes have been severely hindered. Here, an artificial enzyme, PTT-SGH, with responsiveness to reactive oxygen species (ROS), was obtained by introducing a catalytic histidine residue to pentaerythritol tetra(3-mercaptopropionate) (PTT). The artificial enzyme formed large aggregates in cells via the intracellular ROS-mediated oxidation of thiol groups. The process was significantly facilitated in tumor cells because of the higher ROS concentration in the tumor microenvironment. The catalytic activity of this artificial enzyme was intensively enhanced through deprotonation of cross-linked PTT-SGH, which showed typical esterase activities. Selective fluorescence imaging of tumor cells was achieved using the artificial enzyme to trigger the cleavage of the ester bond of the caged fluorophore inside living cells.

Conflict of interest

The authors declare no conflict of interest.

Data Availability Statement

Research data are not shared.

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