Shandong Provincial Key Laboratory of Detection Technology for Tumor Makers, College of Chemistry and Chemical Engineering, Linyi University , Linyi 276005, People's Republic of China.
Shandong Province Key Laboratory of Life-Organic Analysis, College of Chemistry and Chemical Engineering, Qufu Normal University , Qufu 273165, People's Republic of China.
Anal Chem. 2016 Nov 1;88(21):10540-10546. doi: 10.1021/acs.analchem.6b02620. Epub 2016 Oct 21.
The accurate discrimination of microRNAs (miRNAs) with highly similar sequences would greatly facilitate the screening and early diagnosis of diseases. In the present work, a locked nucleic acid (LNA)-modified probe was designed and used for α-hemolysin (α-HL) nanopore to selectively and specifically identify miRNAs. The hybridization of the LNA probe with the target miRNAs generated unique long-lived signals in the nanopore thus facilitated an accurate discrimination of miRNAs with similar sequences, even a single-nucleotide difference. Furthermore, the developed nanopore-based analysis with LNA probe could selectively detect target miRNAs in a natural serum background. This selective and sensitive approach may be highly valuable in the detection of clinically relevant biomarkers in complex samples.
准确区分具有高度相似序列的 microRNAs (miRNAs) 将极大地促进疾病的筛查和早期诊断。在本工作中,设计了一种锁核酸 (LNA)-修饰的探针,并用于 α-溶血素 (α-HL) 纳米孔,以选择性和特异性地识别 miRNAs。LNA 探针与靶 miRNAs 的杂交在纳米孔中产生独特的长寿命信号,从而能够准确区分具有相似序列的 miRNAs,即使存在单个核苷酸差异。此外,基于 LNA 探针的纳米孔分析可以在天然血清背景下选择性地检测靶 miRNAs。这种选择性和灵敏的方法在复杂样品中检测临床相关生物标志物可能具有很高的价值。