| Literature DB >> 31449353 |
Fang Hu1, Guobin Qi1, Duo Mao1, Shiwei Zhou1, Min Wu1, Wenbo Wu1, Bin Liu1.
Abstract
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.Entities:
Keywords: aggregation-induced emission; intracellular bacteria; light-up probes; metabolic labeling; photodynamic ablation
Year: 2019 PMID: 31449353 DOI: 10.1002/anie.201910187
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336