共 21 条
Promoting the healing of methicillin-resistant Staphylococcus aureus-infected wound by a multi-target antimicrobial AIEgen of 6-Aza-2-- thiothymine-decorated gold nanoclusters
被引:5
|作者:
Zhuang, Quan-Quan
[1
,2
]
Yang, Jia-Lin
[2
]
Qiu, Hui-Na
[3
]
Huang, Kai-Yuan
[2
]
Yang, Yu
[2
]
Peng, Hua-Ping
[2
]
Deng, Hao-Hua
[2
]
Jiang, Hui-Qiong
[4
]
Chen, Wei
[2
]
机构:
[1] Fujian Med Univ, Dept Pharm, Quanzhou Hosp 1, Quanzhou 362000, Peoples R China
[2] Fujian Med Univ, Sch Pharm, Fujian Key Lab Drug Target Discovery & Struct & Fu, Fuzhou 350004, Peoples R China
[3] Quanzhou Infect Dis Hosp, Dept Lab Med, Quanzhou 362000, Peoples R China
[4] Fujian Med Univ, Dept Cardiac Funct Examinat Room, Quanzhou Hosp 1, Quanzhou 362000, Peoples R China
关键词:
6-Aza-2-thiothymine-decorated gold;
nanoclusters;
Antimicrobial AIEgen;
Multipletarget;
Wound-healing;
METAL NANOCLUSTERS;
ANTIBACTERIAL;
NANOMATERIALS;
D O I:
10.1016/j.colsurfb.2023.113336
中图分类号:
Q6 [生物物理学];
学科分类号:
071011 ;
摘要:
The use of conventional antibiotic therapies is in question owing to the emergence of drug-resistant pathogenic bacteria. Therefore, novel, highly efficient antibacterial agents to effectively overcome resistant bacteria are urgently needed. Accordingly, in this work, we described a novel class luminogen of 6-Aza-2-thiothymine-decorated gold nanoclusters (ATT-AuNCs) with aggregation-induced emission property that possessed potent antimicrobial activity against methicillin-resistant Staphylococcus aureus (MRSA). Scanning electron microscopy was performed to investigate the interactions between ATT-AuNCs and MRSA. In addition, ATT-AuNCs exhibited excellent ROS generation efficiency and could effectively ablate MRSA via their internalization to the cells. Finally, tandem mass tag-labeling proteome analysis was carried out to investigate the differential expression proteins in MRSA strains. The results suggested that ATT-AuNCs killed MRSA cells through altering the expression of multiple target proteins involved in DNA replication, aminoacyl-tRNA synthesis, peptidoglycan and arginine biosynthesis metabolism. Parallel reaction monitoring technique was further used for the validation of these proteome results. ATT-AuNCs could also be served as a wound-healing agent and accelerate the healing process. Overall, we proposed ATT-AuNCs could serve as a robust antimicrobial aggregation-induced emission luminogen (AIEgen) that shows the ability to alter the activities of multiple targets for the elimination of drugresistant bacteria.
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