Shao Shuxuan, Du Wei, Liu Shuang, Hu Canqiong, Zhang Cao, Li Lexun, Yang Fan, Liu Qiaoling, Tan Weihong
Molecular Science and Biomedicine Laboratory (MBL), State Key Laboratory of Chemo/Biosensing and Chemometrics, FuRong Laboratory, College of Biology, Hunan University, Changsha, Hunan 410082, China.
Department of Pathology, Changde Hospital, Xiangya School of Medicine, Central South University (The First People's Hospital of Changde City), Changde, Hunan 415000, China.
ACS Cent Sci. 2024 Dec 5;10(12):2338-2345. doi: 10.1021/acscentsci.4c01152. eCollection 2024 Dec 25.
Amphiphilic lipid oligonucleotide conjugates are powerful molecular-engineering materials that have been used for delivery of therapeutic oligonucleotides. However, conventional lipid oligonucleotide conjugates suffer from poor selectivity to target cells due to the nonspecific interaction between lipid tails and cell membranes. Herein, a reconfigurable DNA nanotweezer consisting of a c-Met aptamer and bischolesterol-modified antisense oligonucleotide was designed for c-Met-targeted delivery of therapeutic antisense oligonucleotides. The c-Met aptamer is used to keep the DNA nanotweezer in a "closed" state, which enables the hydrophobic interaction within bischolesterol moieties. As a result, the amphiphilic DNA nanotweezer shows only a weak interaction with the cell membrane. Upon the release of the c-Met aptamer, the DNA nanotweezer converts to an "open" state, which facilitates the insertion of a cholesterol moiety into the cell membrane. Thus, the reconfigurable DNA nanotweezer enables the selective membrane anchoring of the DNA nanotweezer in cancerous cells that highly expressed c-Met protein. Moreover, this amphiphilic DNA nanotweezer shows enhanced accumulation at the tumor site and the inhibition of tumor growth. Taking advantage of the stimuli-responsive membrane anchoring capability, this reconfigurable DNA nanotweezer could be further explored as a smart multifunctional platform for cancer therapy.
两亲性脂质寡核苷酸缀合物是强大的分子工程材料,已被用于递送治疗性寡核苷酸。然而,由于脂质尾部与细胞膜之间的非特异性相互作用,传统的脂质寡核苷酸缀合物对靶细胞的选择性较差。在此,设计了一种由c-Met适配体和双胆固醇修饰的反义寡核苷酸组成的可重构DNA纳米镊子,用于靶向递送治疗性反义寡核苷酸至c-Met。c-Met适配体用于使DNA纳米镊子保持在“闭合”状态,这使得双胆固醇部分内能够发生疏水相互作用。结果,两亲性DNA纳米镊子与细胞膜仅表现出微弱的相互作用。当c-Met适配体释放后,DNA纳米镊子转变为“开放”状态,这有利于胆固醇部分插入细胞膜。因此,可重构DNA纳米镊子能够使DNA纳米镊子选择性地锚定在高表达c-Met蛋白的癌细胞膜上。此外,这种两亲性DNA纳米镊子在肿瘤部位的积累增强,并能抑制肿瘤生长。利用这种刺激响应性膜锚定能力,这种可重构DNA纳米镊子可进一步探索作为癌症治疗的智能多功能平台。