适体
化学
超分子化学
皂甙
细胞内
组合化学
单体
生物物理学
分子识别
环糊精
合理设计
纳米技术
生物化学
细胞毒性
分子生物学
分子
体外
生物
聚合物
材料科学
有机化学
免疫毒素
作者
Ying Jiang,Xiaoshu Pan,Jin Chang,Weijia Niu,Weijia Hou,Hailan Kuai,Zilong Zhao,Ji Liu,Ming Wang,Weihong Tan
摘要
Circular bivalent aptamers (cb-apt) comprise an emerging class of chemically engineered aptamers with substantially improved stability and molecular recognition ability. Its therapeutic application, however, is challenged by the lack of functional modules to control the interactions of cb-apt with therapeutics. We present the design of a β-cyclodextrin-modified cb-apt (cb-apt-βCD) and its supramolecular interaction with molecular therapeutics via host-guest chemistry for targeted intracellular delivery. The supramolecular ensemble exhibits high serum stability and enhanced intracellular delivery efficiency compared to a monomeric aptamer. The cb-apt-βCD ensemble delivers green fluorescent protein into targeted cells with efficiency as high as 80%, or cytotoxic saporin to efficiently inhibit tumor cell growth. The strategy of conjugating βCD to cb-apt, and subsequently modulating the supramolecular chemistry of cb-apt-βCD, provides a general platform to expand and diversify the function of aptamers, enabling new biological and therapeutic applications.
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