College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha 410128, China.
Analyst. 2019 Mar 11;144(6):2173-2178. doi: 10.1039/c8an02340a.
In this work, a label-free fluorescence biosensor for simple detection of the HIV-1 gene was proposed by using toehold-mediated strand displacement reactions (TMSDRs) combined with a non-enzymatic target recycling amplification strategy. In this system, two TMSDRs were used. In the presence of the HIV-1 gene, an autocatalytic DNA machine can be activated. This leads to the generation of numerous free G-rich sequences, which can associate with a fluorescent dye N-methylmesoporphyrin IX (NMM) to yield an amplified fluorescence signal for the target detection. This sensing platform showed a high sensitivity towards the HIV-1 gene with a detection limit as low as 1.9 pM without any labelling, immobilization, or washing steps. The designed sensing system also exhibits an excellent selectivity for the HIV-1 gene compared with other interference DNA sequences. Furthermore, the presented biosensor is robust and has been successfully applied for the detection of the HIV-1 gene in a real biological sample with satisfactory results, suggesting that this method is promising for simple and early clinical diagnosis of HIV infection. Thanks to its simplicity, cost-effectiveness and ultrasensitivity, our proposed sensing strategy provides a universal platform for the detection of other genes by substituting the target-recognition element.
在这项工作中,提出了一种无标记荧光生物传感器,用于简单检测 HIV-1 基因,该传感器结合了链置换反应(TMSDR)和非酶靶标循环放大策略。在该系统中使用了两种 TMSDR。在 HIV-1 基因存在的情况下,可以激活自动催化 DNA 机器。这导致产生大量游离的 G 丰富序列,其可以与荧光染料 N-甲基甲川卟啉 IX(NMM)结合,从而产生针对靶标检测的放大荧光信号。与其他干扰 DNA 序列相比,该传感平台对 HIV-1 基因具有很高的灵敏度,检测限低至 1.9 pM,而无需任何标记、固定或洗涤步骤。与其他干扰 DNA 序列相比,所设计的传感系统对 HIV-1 基因也表现出优异的选择性。此外,所提出的生物传感器具有稳健性,并已成功应用于真实生物样品中 HIV-1 基因的检测,结果令人满意,表明该方法有望用于 HIV 感染的简单和早期临床诊断。由于其简单性、成本效益和超灵敏性,我们提出的传感策略通过取代靶标识别元件为其他基因的检测提供了通用平台。