纳米器件
化学
细胞质
DNA
核酸
寡核苷酸
小分子
纳米技术
胞浆
基因传递
细胞生物学
细胞内
生物物理学
生物化学
转染
基因
生物
酶
材料科学
作者
Yu Lu,Yang Xu,Md Al‐Amin,Shuoxing Jiang,Matthew Sample,Abhay Prasad,Nicholas Stephanopoulos,Petr Šulc,Hao Yan
摘要
Direct and efficient delivery of functional payloads such as chemotherapy drugs, siRNA, or small-molecule inhibitors into the cytoplasm, bypassing the endo/lysosomal trapping, is a challenging task for intracellular medicine. Here, we take advantage of the programmability of DNA nanotechnology to develop a DNA nanodevice called CytoDirect, which incorporates disulfide units and human epidermal growth factor receptor 2 (HER2) affibodies into a DNA origami nanostructure, enabling rapid cytosolic uptake into targeted cancer cells and deep tissue penetration. We further demonstrated that therapeutic oligonucleotides and small-molecule chemotherapy drugs can be easily delivered by CytoDirect and showed notable effects on gene knockdown and cell apoptosis, respectively. This study demonstrates the synergistic effect of disulfide and HER2 affibody modifications on the rapid cytosolic delivery of DNA origami and its payloads to targeted cells and deep tissues, thereby expanding the delivery capabilities of DNA nanostructures in a new direction for disease treatment.
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