Nanoengineered Peptide-Grafted Hyperbranched Polymers for Killing of Bacteria Monitored in Real Time via Intrinsic Aggregation-Induced Emission

被引:60
作者
Zhao, Jianliang [1 ]
Dong, Zhenzhen [1 ]
Cui, Hanrui [1 ]
Jin, Hongwei [2 ]
Wang, Caiqi [1 ]
机构
[1] Univ Chinese Acad Sci, Sch Chem Sci, Beijing 100049, Peoples R China
[2] Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
nanoengineered; hyperbranched; antimicrobial peptide polymers; aggregation-induced emission; bacteria imaging; ANTIMICROBIAL PEPTIDES; NANOSTRUCTURES; NANOPARTICLES; FLUORESCENCE; ANTIBIOTICS; MECHANISM; FUNCTIONALITY; CYTOTOXICITY; DENDRIMERS; EVOLUTION;
D O I
10.1021/acsami.8b15921
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Facing the global health crisis caused by drug-resistant bacteria, antimicrobial peptides and their analogues offer exciting solutions to this widespread problem. Without additionally introducing a fluorescent probe, novel nanoengineered peptide-grafted hyperbranched polymers (NPGHPs) are constructed for their combined outstanding antimicrobial activity and sensitive bacterial detection in real time. Hyperbranched polyamide amine (H-PAMAM) that exhibits aggregation-induced emission (AIE) effects is synthesized. Then, NPGHPs are prepared by ring-opening polymerization of alpha-amino acid N-carboxyanhydrides on the periphery of the H-PAMAM. The NPGHPs exhibit high-efficiency antibacterial properties against a wide spectrum of bacteria, especially against Gram-negative bacteria. On the basis of the AIE effect of NPGHPs, the interaction between NPGHPs and Escherichia coli is explored and the fluorescence intensity of NPGHPs is dependent on the number of E. coli present. Thus, a method for monitoring E. coli concentration is developed, and the detection limit is 1 x 10(4) CFU mL(-1). Furthermore, NPGHPs are used as fluorescent probes to visualize antibacterial process via lighting-up bacteria. NPGHPs can penetrate the membrane of bacteria and cause cell rupture and apoptosis. In addition, the excellent selectivity of NPGHPs toward bacteria over mammalian cells makes them bright prospects for clinical applications.
引用
收藏
页码:42058 / 42067
页数:10
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