Goodchild Sarah A, Gao Rachel, Shenton Daniel P, McIntosh Alastair J S, Brown Tom, Bartlett Philip N
Defence Science and Technology Laboratory, Salisbury, United Kingdom.
University of Southampton, Southampton, United Kingdom.
Front Chem. 2020 May 12;8:381. doi: 10.3389/fchem.2020.00381. eCollection 2020.
A novel electrochemical detection approach using DNA probes labeled with Anthraquinone (AQ) as a reporter moiety has been successfully exploited as a method for the direct detection of DNA targets. This assay uses simple voltammetry techniques (Differential Pulse Voltammetry) to exploit the unique responsiveness of AQ to its chemical environments within oxygenated aqueous buffers, providing a specific detection mechanism as a result of DNA hybridization. This measurement is based on a cathodic shift of the reduction potential of the AQ tag and the concurrent reduction in peak current upon DNA binding. The further utility of this approach for discrimination of closely related DNA targets is demonstrated using DNA strands specific to and closely related bacillus species. DNA targets were designed to the B gene incorporating nucleotide polymorphisms associated with different bacillus species. This assay was used to demonstrate that the shift in reduction potential is directly related to the homology of the target DNA. The discriminatory mechanism is dependent on the presence of oxygen in the measurement buffer and is strongly linked to the position of the nucleotide polymorphisms; with homology at the terminus carrying the AQ functionalised nucleotide critical to achieving accurate discrimination. This understanding of assay design was used to demonstrate an optimized assay capable of discriminating between (the causative agent of plague) and closely related species based on the EL gene. This method is attractive as it can not only detect DNA binding, but can also discriminate between multiple Single Nucleotide Polymorphisms (SNPs) within that DNA without the need for any additional reagents, reporters, or processes such as melting of DNA strands. This indicates that this approach may have great potential to be exploited within novel biosensors for detection and diagnosis of infectious disease in future Point of Care (PoC) devices.
一种新型电化学检测方法已成功开发出来,该方法使用以蒽醌(AQ)作为报告基团标记的DNA探针直接检测DNA靶标。此检测方法采用简单的伏安法技术(差分脉冲伏安法),利用AQ在含氧水性缓冲液中对其化学环境的独特响应性,通过DNA杂交提供一种特异性检测机制。该测量基于AQ标签还原电位的阴极移动以及DNA结合时峰值电流的同时降低。使用针对特定和密切相关芽孢杆菌属物种的DNA链,证明了该方法在区分密切相关DNA靶标方面的进一步实用性。针对包含与不同芽孢杆菌属物种相关的核苷酸多态性的B基因设计了DNA靶标。该检测方法用于证明还原电位的变化与靶标DNA的同源性直接相关。鉴别机制取决于测量缓冲液中氧气的存在,并且与核苷酸多态性的位置密切相关;在携带AQ功能化核苷酸的末端具有同源性对于实现准确鉴别至关重要。对检测设计的这种理解用于证明一种优化的检测方法,该方法能够基于EL基因区分鼠疫耶尔森菌(鼠疫病原体)和密切相关的物种。这种方法具有吸引力,因为它不仅可以检测DNA结合,还可以区分该DNA内的多个单核苷酸多态性(SNP),而无需任何额外的试剂、报告分子或诸如DNA链解链等过程。这表明这种方法在未来的即时检测(PoC)设备中的新型生物传感器中用于传染病检测和诊断方面可能具有巨大的开发潜力。