化学
小RNA
荧光
核糖核酸
生物分子
小发夹RNA
复式(建筑)
核酸
体内
适体
检出限
寡核苷酸
纳米技术
催化作用
生物物理学
计算生物学
体外
组合化学
RNA干扰
信使核糖核酸
细胞生物学
生物化学
绿色荧光蛋白
荧光素酶
荧光显微镜
分子生物学
原位
线性范围
作者
Jun‐Yi Yang,Mingli Su,Wei-Guo Yang,Ruiwen Wang,Rui Jin,Jia-Min Qin,Ruo Yuan,Ying Zhuo,Ping Li,Wenbin Liang
标识
DOI:10.1021/acs.analchem.5c04052
摘要
MicroRNA (miRNA), as a small noncoding RNA dysregulated in various cancers, can be considered an efficient biomarker for early diagnosis. Herein, we proposed a label-free fluorescent RNA-based catalytic hairpin assembly strategy to monitor miRNA in vivo and in vitro accurately with highly efficient performances. In the presence of target miRNA, it could activate the catalytic hairpin assembly (CHA) cycle by hybridizing with H1 and H2 to form an H1-H2 duplex complex and release target miRNA for cyclic amplification, while the H2 structure was induced into a fluorescence-active conformation in the H1-H2 duplex with a stable aptamer domain to react with a fluorescent molecule, generating a robust fluorescence response related with the concentration of target miRNA. Thus, the fluorescent RNA-based catalytic hairpin assembly system realizes the cyclic amplification with label-free fluorescent RNA (FLRNA), which produces simpler, efficient, and ultrahighly sensitive analytical capabilities, especially good linearity in the concentration range from 1 pM to 1 nM with a detection limit of 0.65 pM, opening a new door to monitor the expression levels of biomolecules for early diagnosis and prognostic assessment of a variety of diseases.
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