金融时报
核酸
金黄色葡萄球菌
流出
感应(电子)
微生物学
药物输送
肽
肽核酸
DNA
化学
基因传递
细菌
生物
寡核苷酸
基因
生物化学
大肠杆菌
转染
遗传学
有机化学
物理化学
作者
Yuxin Zhang,Wenjuan Ma,Ying Zhu,Sirong Shi,Qianshun Li,Chenchen Mao,Dan Zhao,Yuxi Zhan,Jiye Shi,Wei Li,Lihua Wang,Chunhai Fan,Yunfeng Lin
出处
期刊:Nano Letters
[American Chemical Society]
日期:2018-08-08
卷期号:18 (9): 5652-5659
被引量:133
标识
DOI:10.1021/acs.nanolett.8b02166
摘要
One of the biggest obstacles for the use of antisense oligonucleotides as antibacterial therapeutics is their limited uptake by bacterial cells without a suitable carrier, especially in multi-drug-resistant bacteria with a drug efflux mechanism. Existing vectors, such as cell-penetrating peptides, are inefficient and nontargeting, and accordingly are not ideal carriers. A noncytotoxic tetrahedral DNA nanostructure (TDN) with a controllable conformation has been developed as a delivery vehicle for antisense oligonucleotides. In this study, antisense peptide nucleic acids (asPNAs) targeting a specific gene (ftsZ) were efficiently transported into methicillin-resistant Staphylococcus aureus cells by TDNs, and the expression of ftsZ was successfully inhibited in an asPNA-concentration-dependent manner. The delivery system specifically targeted the intended gene. This novel delivery system provides a better platform for future applications of antisense antibacterial therapeutics and provides a basis for the development of a new type of antibacterial drug for multi-drug-resistant bacterial infections.
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