4.7 Article

A colorimetric biosensor for detection of attomolar microRNA with a functional nucleic acid-based amplification machine

Journal

TALANTA
Volume 146, Issue -, Pages 470-476

Publisher

ELSEVIER
DOI: 10.1016/j.talanta.2015.09.010

Keywords

Colorimetric biosensing; Signal amplification; Toehold initiated rolling circle amplification; DNAzyme; MicroRNA

Funding

  1. National Basic Research Program [2010CB732400]
  2. National Natural Science Foundation of China [21135002, 81371904, 81101638]
  3. Natural Science Foundation Project of CQ [CSTC2013jjB10019]
  4. Research Fund for Postgraduate Innovation Project of Chongqing [CYB14080]

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A functional nucleic acid-based amplification machine was designed for simple and label-free ultrasensitive colorimetric biosensing of microRNA (miRNA). The amplification machine was composed of a complex of trigger template and C-rich DNA modified molecular beacon (MB) and G-rich DNA (GDNA) as the probe, polymerase and nicking enzyme, and a dumbbell-shaped amplification template. The presence of target miRNA triggered MB mediated strand displacement to cyclically release nicking triggers, which led to a toehold initiated rolling circle amplification to produce large amounts of GDNAs. The formed GDNAs could stack with hemin to form G-quadruplex/hemin DNAzyme, a well-known horseradish peroxidase (HRP) mimic, for catalyzing a colorimetric reaction. The modified MB improved the stringent target recognition and reduced background signal. The proposed sensing strategy showed very high sensitivity and selectivity with a wide dynamic range from 10 aM to 1.0 nM, and enabled successful visual analysis of trace amount of miRNA in real sample by the naked eye. This rapid and highly efficient signal amplification strategy provided a simple and sensitive platform for miRNA detection. It would be a versatile and powerful tool for clinical molecular diagnostics. (C) 2015 Elsevier B.V. All rights reserved.

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