A dual-signal amplification strategy based on rolling circle amplification and APE1-assisted amplification for highly sensitive and specific miRNA analysis for early diagnosis of alzheimer's disease

化学 滚动圆复制 哑铃 小RNA 生物标志物 计算生物学 检出限 分子生物学 生物 生物化学 基因 色谱法 生理学 DNA复制
作者
Juan Xie,Jing Chen,Jing Chen,Ya Zhang,Changhong Li,Piao Liu,Wen‐Jun Duan,Jin-Xiang Chen,Jin-Xiang Chen,Jun Chen,Jun Chen,Zong Dai,Minmin Li
出处
期刊:Talanta [Elsevier BV]
卷期号:272: 125747-125747 被引量:17
标识
DOI:10.1016/j.talanta.2024.125747
摘要

MicroRNA (miRNA) is involved in the progression of Alzheimer's disease (AD) and emerges as a promising AD biomarker and therapeutic target. Therefore, there is an urgent need to develop convenient and precise miRNA detection methods for AD diagnosis. Herein, a dual-signal amplification strategy based on rolling circle amplification and APE1-assisted amplification for miRNA analysis for early diagnosis of AD was proposed. The strategy consisted of dumbbell-shaped probe (DP) as amplification template and a reporter probe (RP) with an AP site modification. In the presence of the target miRNA, the miRNAs bound to the toehold domain of DP and DP was activated into a circular template. Then, RCA reaction was triggered, producing a large number of long-stranded products containing repeated sequences. After RCA, APE1 enzyme recognized and removed AP site in the complex of RCA/RP products. By coupling RCA with APE1-assisted amplification, this method has high sensitivity with the limit of detection (LOD) of 1.82 fM. Moreover, by using DP as template for RCA reaction, high specificity can be achieved. By detecting miR-206 in serum using this method, the expression of miR-206 can be accurately distinguished between AD patients and healthy individuals, indicating that this method has broad application prospects in clinical diagnosis.
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