Colorimetric detection of microRNA based hybridization chain reaction for signal amplification and enzyme for visualization

• Published in: Analytical biochemistry Vol. 528; pp. 7 - 12
• Main Authors: Ying, Na, Sun, Taifan, Chen, Zhibao, Song, Guangping, Qi, Bingyao, Bu, Shengjun, Sun, Xiuwei, Wan, Jiayu, Li, Zehong
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01-07-2017
• Subjects: Benzidines - chemistry; Biosensing Techniques; Colorimetric detection; Colorimetry - methods; Fluorescent Dyes - chemistry; Horseradish peroxidase; Horseradish Peroxidase - chemistry; Humans; Hybridization chain reaction; Hydrogen Peroxide - chemistry; Limit of Detection; Microplate; MicroRNAs - analysis; MicroRNAs - blood; MicroRNAs - genetics; miRNAs; Nucleic Acid Hybridization; Sensitivity and Specificity; Horseradish peroxidase; Microplate; Hybridization chain reaction; miRNAs; Colorimetric detection
• ISSN: 0003-2697; 1096-0309
• DOI: 10.1016/j.ab.2017.04.007

MicroRNAs (miRNAs) have key roles in gene expression and can be employed as biomarkers for early diagnosis of various diseases, especially cancers. Detection of miRNAs remains challenging and often requires detection platforms. Here, a horseradish peroxidase (HRP)-assisted hybridization chain reaction (HCR) for colorimetric detection of miR-155 was described. In the presence of target miRNA, the capture probe immobilized on the microplate sandwiched the target miR-155 with the 3′ end of the reporter probe. Another exposed part of the RP at the 5'end triggered HCR producing double-stranded DNA polymers with multiple fluorescein isothiocyanates (FITC) for signal amplification. Finally, multiple HRP molecules were immobilized onto the long-range DNA nanostructures through FITC/anti-FITC monoclonal antibody interactions on the microplate for visualization by tetramethylbenzidine/H2O2 system and the colorless substrate turned into the blue product. To obtain accurate data, the absorbance at 450 nm was calculated by microplate reader. The detection limit was 31.8 fM (3.18 amol). Furthermore, this biosensor showed high specificity and was able to discriminate sharply between target miRNA and mismatched sequences. And this approach could be easily applied to the detection of miR-155 in serum sample, thereby ascribing it for a wide application.