核糖核酸
DNA
化学
脱氧核酶
核酸酶
纳米片
核糖核酸酶P
核糖核酸酶H
杂交探针
生物物理学
组合化学
分子信标
杰纳斯
纳米技术
寡核苷酸
生物化学
生物
基因
有机化学
材料科学
作者
Feng Chen,Min Bai,Yue Zhao,Ke Cao,Xiaowen Cao,Yongxi Zhao,Yongxi Zhao,Yongxi Zhao
标识
DOI:10.1021/acs.analchem.7b04634
摘要
Both biomarker and probe degradations cause serious false assay results. However, protecting a target or a target and a probe simultaneously has rarely been explored. Herein, MnO 2 -nanosheet-powered target- and probe-protective Janus DNA nanomachines are reported. It is formed in living cells by an RNA-responsive assembly of two chemically modified DNA partzymes and one substrate probe. MnO 2 nanosheets are used to facilitate the cellular uptake of DNA reagents and generate Mn 2+, which are indispensable DNAzyme cofactors for efficient catalytic cleavage. We find that DNA partzymes with modified sugar moieties (e.g., LNA or ones with 2′-O-methylation) protect the RNA of RNA–DNA hybrids from RNase H degradation. LNA blocks RNase H recruitment on the hybrid best because of its 2′-O, 4′-C methylene bridge structure. In contrast, modifications at DNA phosphate moieties fail to protect the RNA. RNA protection can exclude target-degradation-induced false negative results. In addition, the phosphorothioate-modified substrate probe is known to resist nuclease degradation, which minimizes false positive interference. Compared to canonical DNA systems without chemical modifications, the protective Janus nanomachine avoids false results and supports robust RNA imaging.
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