Low-cost colorimetric reader and label-free strategy for user-friendly detection of nucleic acid amplification products

核酸 色谱法 化学 DNA 核酸法 核酸定量 生物化学
作者
Wenzhi Tang,Meng Zhang,Tianli Yue,Xin Wang,Zhonghong Li
出处
期刊:Sensors and Actuators B-chemical [Elsevier BV]
卷期号:346: 130523-130523 被引量:3
标识
DOI:10.1016/j.snb.2021.130523
摘要

• Rapid and simple analysis of polymerase chain reaction (PCR) products. • Colorimetric detection of PCR products with the simplicity of visual detection. • Low-cost device and reagents for label-free analysis of PCR products. • PCR tube as a disposable cuvette for colorimetric analysis of PCR products. • Comparable sensitivity and specificity as the professional method. Analyses of nucleic acid amplification products are generally performed by the complicated gel electrophoresis or costly florescence method. In this work, colorimetric detection of phosphate ions (Pis) generated in the amplification reaction was proposed for user-friendly and low-cost detection of nucleic acid products. To overcome the interference from nonspecific Pis, the effects of deoxyribonucleoside triphosphates (dNTPs) and Mg 2+ concentrations, thermal cycle and initial template were investigated. The results showed that the yields of nonspecific Pis were constant, reproducible, and was the same at the presence/absence of target template, suggesting the potential to simply measure and subtract the interference. A colorimetric reader was developed to detect Pis in the amplification tube. It revealed that the unique structure of the tube would diverge, merge and reflect the transmitting light depending on the volume of solution, and could provide dependable results when the volume was higher than 160 μL. Measurements of Staphylococcus aureus demonstrated detection limits of 10 4 copies μL −1 for genomic DNA nuc and 2.2 × 10 1 CFU mL −1 for milk cultured with 8 h. This method showed comparable sensitivity as the gel electrophoresis, avoided complicated operations and reduced the cost, demonstrating a promising potential to facilitate the detection of nucleic acid products.
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