药物输送
纳米技术
DNA
适体
生物相容性
材料科学
核酸酶
组合化学
化学
生物物理学
生物
生物化学
有机化学
遗传学
作者
Tao Zhang,Taoran Tian,Ronghui Zhou,Songhang Li,Wen‐Juan Ma,Yuxin Zhang,Бо Лю,Sirong Shi,Qianshun Li,Xueping Xie,Yichen Ge,Mengting Liu,Qi Zhang,Shiyu Lin,Xiaoxiao Cai,Yunfeng Lin
出处
期刊:Nature Protocols
[Springer Nature]
日期:2020-07-15
卷期号:15 (8): 2728-2757
被引量:263
标识
DOI:10.1038/s41596-020-0355-z
摘要
Although organic nanomaterials and inorganic nanoparticles possess inherent flexibility, facilitating functional modification, increased intracellular uptake and controllable drug release, their underlying cytotoxicity and lack of specificity still cause safety concerns. Owing to their merits, which include natural biocompatibility, structural stability, unsurpassed programmability, ease of internalization and editable functionality, tetrahedral DNA nanostructures show promising potential as an alternative vehicle for drug delivery and biomedical treatment. Here, we describe the design, fabrication, purification, characterization and potential biomedical applications of a self-assembling tetrahedral DNA nanostructure (TDN)-based multifunctional delivery system. First, relying on Watson-Crick base pairing, four single DNA strands form a simple and typical pyramid structure via one hybridization step. Then, the protocol details four different modification approaches, including replacing a short sequence of a single DNA strand by an antisense peptide nucleic acid, appending an aptamer to the vertex, direct incubation with small-molecular-weight drugs such as paclitaxel and wogonin and coating with protective agents such as cationic polymers. These modified TDN-based complexes promote the intracellular uptake and biostability of the delivered molecules, and show promise in the fields of targeted therapy, antibacterial and anticancer treatment and tissue regeneration. The entire duration of assembly and characterization depends on the cargo type and modification method, which takes from 2 h to 3 d.
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