化学
核酸
检出限
生物传感器
溶解
纳米技术
DNA
荧光
小RNA
组合化学
计算生物学
分子生物学
生物化学
色谱法
基因
材料科学
物理
量子力学
生物
作者
Hongfeng Li,Yang Li,Wenqin Li,Liang Cui,Guohua Huang,Jiahao Huang
出处
期刊:Talanta
[Elsevier BV]
日期:2020-02-14
卷期号:213: 120816-120816
被引量:27
标识
DOI:10.1016/j.talanta.2020.120816
摘要
Nucleic acid-based biosensors have become powerful tools in biomedical applications. But the stability issue seriously limits their wide applications. Fortunately, the emergence of carbon nanoparticles (CNPs), which can effectively protect DNA probes from enzymatic digestion and unspecific protein binding, provides a good solution. In this work, a DNase I-aided cyclic enzymatic amplification method (CEAM) for microRNA analysis has been developed based on the coupling use of nucleic acid probes with specific molecular recognition ability as well as CNPs with excellent biostability. The method is simple and sensitive, with a detection limit down to 3.2 pM. Furthermore, satisfactory results are achieved for miRNA analysis in breast cancer cell lysate, demonstrating the applicability in disease diagnosis. The ingenious combination of CNPs and nucleic acid probes can open a new chapter in the development of versatile analytical strategies that holds great potentials for clinical diagnosis, food safety, and environmental monitoring.
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