菁
化学
核酸
费斯特共振能量转移
纳米载体
DNA
内化
环介导等温扩增
纳米技术
生物物理学
动力学
转染
细胞内
连锁反应
荧光
计算生物学
分子生物学
药物输送
生物化学
细胞
物理
材料科学
有机化学
光化学
量子力学
生物
基因
作者
Liuting Mo,Danlian Liang,Runhong Qin,Mingxiu Mo,Chan Yang,Weiying Lin
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2023-07-28
卷期号:95 (31): 11777-11784
被引量:39
标识
DOI:10.1021/acs.analchem.3c02014
摘要
Isothermal, enzyme-free amplification techniques, such as the hybridization chain reaction (HCR) and catalytic hairpin assembly (CHA), have gained increasing attention for miRNA analysis. However, current methodological challenges, including slow kinetics, low amplification efficiency, difficulties in efficient cellular internalization of DNA probes, and concerns regarding the intracellular stability of nucleic acids, need to be addressed. To this end, we propose a novel strategy for sensitive miRNA detection based on a three-dimensional (3D) CHA-HCR system. This system comprises two DNA nanospheres, named DS-13 and DS-24, which are functionalized with CHA and HCR hairpins. Target miR-21 initiates CHA between the two nanospheres, thereby activating downstream HCR and bringing cyanine 3 (Cy3) and cyanine 5 (Cy5) into proximity. The 3D CHA-HCR process leads to the formation of large DNA aggregates and the generation of fluorescence resonance energy transfer signals. In this strategy, the employment of a cascaded reaction and spatial confinement effect improve sensitivity and kinetics, while the use of DNA nanocarriers facilitates cellular delivery and protects nucleic acid probes. The experimental results in vitro, in living cells, and in clinical tissue samples demonstrated the desirable sensing performance. Collectively, this approach holds promise as a valuable tool for cancer diagnosis and biomedical research.
科研通智能强力驱动
Strongly Powered by AbleSci AI