脱氧核酶
化学
细胞内
辅因子
基质(水族馆)
纳米技术
生物物理学
劈开
DNA
生物传感器
组合化学
生物化学
酶
材料科学
海洋学
生物
地质学
作者
Jiaxin Su,Jinya Du,Rujiao Ge,Chenyang Sun,Yuchun Qiao,Wei Wei,Xuejiao Pang,Yufan Zhang,Huiting Lu,Haifeng Dong
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2022-09-16
卷期号:94 (38): 13108-13116
被引量:21
标识
DOI:10.1021/acs.analchem.2c02547
摘要
DNAzyme shows great promise in designing a highly sensitive and specific sensing platform; however, the low cellular uptake efficiency, instability, and especially the insufficient cofactor supply inhibit the intracellular molecule sensor applications. Herein, we demonstrate a novel type of DNAzyme-based self-driven intracellular sensor for microRNA (miRNA) detection in living cells. The sensor consists of a metal-organic framework [zeolite imidazole framework (ZIF-8)] core loaded with a shell consisting of a rationally designed DNAzyme, where the substrate strand is modified with FAM and BHQ-1 nearby both the sides of the restriction site, respectively, while the enzyme strand consists of two separate strands with a complementary fragment to the substrate strand and the targeting miRNA, respectively. The ZIF-8 nanoparticles enable the efficient delivery of DNAzyme into the cell and protect the DNAzyme from degradation. The pH-responsive ZIF-8 degradation is accompanied with the release of the DNAzyme and Zn2+ cofactors, and the intracellular target miRNAs recognize and activate the DNAzyme driven by the Zn2+ cofactors to cleave the substrate strand, resulting in the release of the FAM-labeled shorter product strand and increased fluorescence for miRNA detection. The self-driven approach can be generally applied to various miRNAs' detection through DNAzyme engineering.
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