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https://doi.org/10.1002/anie.201910187
Title: | Visualization and In Situ Ablation of Intracellular Bacterial Pathogens through Metabolic Labeling | Authors: | Hu, F Qi, G Kenry Mao, D Zhou, S Wu, M Wu, W Liu, B |
Keywords: | aggregation-induced emission intracellular bacteria light-up probes metabolic labeling photodynamic ablation |
Issue Date: | 1-Jan-2019 | Publisher: | Wiley | Citation: | Hu, F, Qi, G, Kenry, Mao, D, Zhou, S, Wu, M, Wu, W, Liu, B (2019-01-01). Visualization and In Situ Ablation of Intracellular Bacterial Pathogens through Metabolic Labeling. Angewandte Chemie - International Edition 59 (24) : 9288-9292. ScholarBank@NUS Repository. https://doi.org/10.1002/anie.201910187 | Abstract: | © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Protected by the host cells, the hidden intracellular bacteria are typically difficult to kill by common antibiotics and cannot be visualized without complex cellular pretreatments. Herein, we successfully developed a bacteria-metabolizable dual-functional probe TPEPy-d-Ala, which is based on d-alanine and a photosensitizer with aggregation-induced emission for fluorescence turn-on imaging of intracellular bacteria in living host cells and photodynamic ablation in situ. Once metabolically incorporated into bacterial peptidoglycan, the intramolecular motions of TPEPy-d-Ala are inhibited, leading to an enhanced fluorescent signal, which allows the clear visualization of the intracellular bacteria. Moreover, TPEPy-d-Ala can effectively ablate the labeled intracellular bacteria in situ owing to covalent ligation to peptidoglycan, yielding a low intracellular minimum inhibitory concentration (MIC) of 20±0.5 μg mL−1, much more efficient than that of a commonly used antibiotic, vancomycin. | Source Title: | Angewandte Chemie - International Edition | URI: | https://scholarbank.nus.edu.sg/handle/10635/169592 | ISSN: | 14337851 15213773 |
DOI: | 10.1002/anie.201910187 |
Appears in Collections: | Elements Staff Publications |
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Hu Fang Angewandte-.pdf | Accepted version | 1.94 MB | Adobe PDF | OPEN | Post-print | View/Download |
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