One-pot, one-step, label-free miRNA detection method based on the structural transition of dumbbell probe

被引:2
|
作者
Jeung, Jae Hoon [1 ,2 ]
Han, Hyogu [1 ,3 ]
Jang, Se Hee [1 ,4 ]
Lee, Chang Yeol [5 ]
Ahn, Jun Ki [1 ]
机构
[1] Korea Inst Ind Technol KITECH, Mat & Component Convergence R&D Dept, Ansan, South Korea
[2] Konkuk Univ, Coll Engn, Dept Biol Engn, Seoul 05029, South Korea
[3] Gangneung Wonju Natl Univ, Dept Chem, Kangnung 25457, South Korea
[4] Yonsei Univ, Coll Med, Dept Med Device Engn & Management, Seoul 03722, South Korea
[5] Korea Res Inst Biosci & Biotechnol KRIBB, Bionanotechnol Res Ctr, 125 Gwahak Ro, Daejeon 34141, South Korea
关键词
miRNA; Dumbbell probe; Structural transition; Light -up RNA aptamer; Rolling circle transcription (RCT); Biosensor; ROLLING CIRCLE AMPLIFICATION; REAL-TIME PCR; MICRORNA; TRANSCRIPTION; DIAGNOSIS;
D O I
10.1016/j.talanta.2024.125944
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this study, we present a one-pot, one-step, label-free miRNA detection method through a structural transition of a specially designed dumbbell-shape probe, initiating a rolling circle transition (RCT). In principle, target miRNA binds to right loop of the dumbbell probe (DP), which allows structural change of the DP to circular form, exposing a sequence complementary to the T7 promoter (T7p) previously hidden within the stem. This exposure allows T7 RNA polymerase to initiate RCT, producing a repetitive Mango aptamer sequence. TO1-biotin, fluorescent dye, binds to the aptamer, inducing a detectable enhancement of fluorescence intensity. Without miR141, the DP stays closed, RCT is prevented, and the fluorescence intensity remains low. By employing this novel strategy, target miRNA was successfully identified with a detection of 73 pM and a dynamic linear range of 0-10 nM. Additionally, the method developed enables one-pot, one-step, and label-free detection of miRNA, demonstrating potential for point-of-care testing (POCT) applications. Furthermore, the practical application of the designed technique was demonstrated by reliably detecting the target miRNA in the human serum sample. We also believe that the conceived approach could be widely used to detect not only miRNAs but also diverse biomolecules by simply replacing the detection probe.
引用
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页数:6
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