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Anal Biochem ; 693: 115594, 2024 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-38897269

RESUMEN

The development of a sensitive and isothermal technique with a greatly enhanced miRNA detection signal is still technically problematic due to the low abundance of miRNA and high sequence similarities with homologous miRNAs. Herein, we propose a novel fluorescence approach for sensitive and reliable miRNA detection by integrating the palindrome sequence mediated target recycling with self-priming assisted signal reaction. In this method, a dual toehold DNA nano-probe (HT) with two functional arms is designed to mediate specific target recognition and signal amplification. In the presence of target miRNA, it binds to the recognition module of HT probe, releasing the "2" sequence to initiate strand displacement amplification (SDA) and a self-priming-induced signal reaction. Based on the elegant design, the proposed method exhibits a wide linear response range exceeding five orders of magnitude and a low limit of detection of 0.96 fM according to the 3δ rule. The non-specific signal is below 5 % for non-target miRNA detection. Taking the merits of excellent sensitivity, desirable specificity, and superior anti-interference ability, the proposed approach shows a promising prospect for detecting miRNAs in complicated biological environments and early diagnosis of diseases.


Asunto(s)
Secuencias Invertidas Repetidas , MicroARNs , Técnicas de Amplificación de Ácido Nucleico , MicroARNs/análisis , MicroARNs/genética , Humanos , Técnicas de Amplificación de Ácido Nucleico/métodos , Límite de Detección , Sondas de ADN/química , Sondas de ADN/metabolismo , Espectrometría de Fluorescencia
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