Black Phosphorus/MnO2 Nanocomposite Disrupting Bacterial Thermotolerance for Efficient Mild-Temperature Photothermal Therapy

被引:30
|
作者
Wang, Feng [1 ]
Wu, Qinghe [1 ]
Jia, Guoping [1 ]
Kong, Lingchi [1 ]
Zuo, Rongtai [1 ]
Feng, Kai [1 ]
Hou, Mengfei [1 ]
Chai, Yimin [1 ]
Xu, Jia [1 ]
Zhang, Chunfu [1 ]
Kang, Qinglin [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 6, Dept Orthoped, Sch Med,Sch Biomed Engn, Shanghai 200030, Peoples R China
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
drug-resistant bacteria; heat shock protein; photothermal therapy; respiratory chain complex; self-cascade nanozyme; HEAT; ATP;
D O I
10.1002/advs.202303911
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The emergence of multi-drug resistant (MDR) pathogens is a major public health concern, posing a substantial global economic burden. Photothermal therapy (PTT) at mild temperature presents a promising alternative to traditional antibiotics due to its biological safety and ability to circumvent drug resistance. However, the efficacy of mild PTT is limited by bacterial thermotolerance. Herein, a nanocomposite, BP@Mn-NC, comprising black phosphorus nanosheets and a manganese-based nanozyme (Mn-NZ) is developed, which possesses both photothermal and catalytic properties. Mn-NZ imparts glucose oxidase- and peroxidase-like properties to BP@Mn-NC, generating reactive oxygen species (ROS) that induce lipid peroxidation and malondialdehyde accumulation across the bacterial cell membrane. This process disrupts unprotected respiratory chain complexes exposed on the bacterial cell membrane, leading to a reduction in the intracellular adenosine triphosphate (ATP) content. Consequently, mild PTT mediated by BP@Mn-NC effectively eliminates MDR infections by specifically impairing bacterial thermotolerance because of the dependence of bacterial heat shock proteins (HSPs) on ATP molecules for their proper functioning. This study paves the way for the development of a novel photothermal strategy to eradicate MDR pathogens, which targets bacterial HSPs through ROS-mediated inhibition of bacterial respiratory chain activity.
引用
收藏
页数:14
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