适体
小RNA
核酸
计算生物学
细胞内
DNA
多路复用
纳米技术
癌细胞
细胞生物学
生物物理学
化学
生物
生物信息学
材料科学
癌症
基因
分子生物学
生物化学
遗传学
作者
Min Li,Chan Li,Wangxin Zhao,Haiyan Jia,Ningfang Wu,Chang Xue,Rong Wu,Zhifa Shen
标识
DOI:10.1016/j.snb.2023.135048
摘要
Designing a multifunctional nucleic acid platform with the ability to identify multiple biomarkers is crucial for accurate molecular diagnostics. Here we reported a dual-target branch-shaped nucleic acid probing (DBNP) system and its targeted delivery for simultaneous analysis of intracellular microRNAs (miRNAs). The system consisted of a cross-shaped DNA scaffold equipped with four hairpin strands and an aptamer strand. The four hairpin strands constituted two catalytic hairpin assembly (CHA) reactions, enabling the system to simultaneously recognize and amplify two kinds of miRNAs. We demonstrated that the cross-shaped DNA scaffold structurally offered a spatial-confinement effect, well-known in increasing the intramolecular collision of the probes and accelerating the CHA reactions, which allows us to resolve multiplex miRNAs profiling with high efficiency by using DBNP system. In addition, because of the inherent character of aptamer capable of specifically binding with cell-membrane receptor, targeted delivery of DBNP system into the unique receptor-positive cells can be realized to detect intracellular miRNAs. The dual miRNA-mediated stimuli-response, operating in parallel with a receptor-specific recognition of target cells, synergistically enhances the accuracy of cell discrimination and cancer diagnosis. This innovative approach holds great promise for advancing the development of cutting-edge signal amplification technologies and biosensors utilized in cancer diagnostics.
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