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A Homogeneous Signal-On Strategy for the Detection of rpoB Genes of Mycobacterium tuberculosis Based on Electrochemiluminescent Graphene Oxide and Ferrocene Quenching

机译:基于电化学发光氧化石墨烯和二茂铁猝灭的结核分枝杆菌rpoB基因检测的均相信号开启策略

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Tuberculosis (TB) remains one of the leading causes of morbidity and mortality all over the world and multidrug resistance TB (MDR-TB) pose a serious threat to the TB control and represent an increasing public health problem. In this work, we report a homogeneous signal-on electrochemiluminescence (ECL) DNA sensor for the sensitive and specific detection of rpoB genes of MDR-TB by using ruthenium(II) complex functionalized graphene oxide (Ru-GO) as suspension sensing interface and ferrocene-labeled ssDNA (Fc-ssDNA) as ECL intensity controller. The ECL of Ru-GO could be effectively quenched by Fc-ssDNA absorbed on the Ru-GO nanosheets. The Ru-GO has good discrimination ability over ssDNA and dsDNA. Mutant ssDNA target responsible for the drug resistant tuberculosis can hybridize with Fc-ssDNA and release Fc-ssDNA from Ru-GO surface, leading to the recovery of ECL. Mutant ssDNA target can be detected in a range from 0.1 to 100 nM with a detection limit of 0.04 nM. The proposed protocol is sensitive, specific, simple, time-saving and polymerase chain reaction free without complicated immobilization, separation and washing steps, which creates a simple but valuable tool for facilitating fast and accurate detection of disease related specific sequences or gene mutations.
机译:结核病(TB)仍然是全世界发病率和死亡率的主要原因之一,耐多药结核病(MDR-TB)对结核病控制构成严重威胁,并代表着日益严重的公共卫生问题。在这项工作中,我们报告了一种均相的电化学发光(ECL)DNA传感器,该传感器通过使用钌(II)复杂功能化氧化石墨烯(Ru-GO)作为悬浮物传感界面,灵敏而特异地检测MDR-TB的rpoB基因。二茂铁标记的ssDNA(Fc-ssDNA)作为ECL强度控制器。 Ru-GO的ECL可以被Ru-GO纳米片吸收的Fc-ssDNA有效地淬灭。 Ru-GO对ssDNA和dsDNA具有良好的区分能力。负责耐药结核的突变ssDNA靶标可与Fc-ssDNA杂交并从Ru-GO表面释放Fc-ssDNA,从而导致ECL的恢复。可以在0.1至100 nM的范围内检测到ssDNA突变体,检测限为0.04 nM。所提出的方案是灵敏的,特异性的,简单的,省时的,并且没有聚合酶链反应,而无需复杂的固定,分离和洗涤步骤,从而创建了一个简单而有价值的工具,可用于快速,准确地检测疾病相关的特定序列或基因突变。

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