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首页> 外文期刊>Analytical chemistry >Single Electrode Genosensor for Simultaneous Determination of Sequences Encoding Hemagglutinin and Neuraminidase of Avian Influenza Virus Type H5N1
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Single Electrode Genosensor for Simultaneous Determination of Sequences Encoding Hemagglutinin and Neuraminidase of Avian Influenza Virus Type H5N1

机译:同时测定H5N1型禽流感病毒血凝素和神经氨酸酶序列的单电极基因传感器

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The duo-genosensor consisting of two different oligonucleotide probes immobilized covalently on the surface of one gold electrode via Au-S bond formation was used for simultaneous determination of two different oligonucleotide targets. One of the probes, decorated on its 5'-end with ferrocene (SH-ssDNA-Fc), is complementary to the cDNA representing a sequence encoding part of H5 hemagglutinin from H5N1 virus. The second probe, decorated on its 5'-end with methylene blue (SH-ssDNA-MB), is complementary to cDNA representing the fragment of N1 neuraminidase from the same virus. The presence of both probes on the surface of gold electrodes was confirmed with Osteryoung square-wave voltammetry (OSWV). The changes in redox activity of both redox active complexes before and after the hybridization process were used as analytical signal. The peak at +400 ± 2 mV was observed in the presence of 40 nM ssDNA used as a target for SH-ssDNA-Fc probe. This peak increased with the increase of concentration of target ssDNA. It indicates the "signal on" mode of analytical signal generation. The peak at -250 ± 4 mV, characteristic for SH-ssDNA-MB probe, was decreasing with the increase of the concentration of the complementary ssDNA target starting from 8 to 100 nM. This indicates the generation of electrochemical signal according to the "signal off' mode. The proposed duo-genosensor is capable of simultaneous, specific, and good sensitivity probing for the sequences derived from genes encoding two main markers of the influenza virus, hemagglutinin and neuraminidase.
机译:由两个通过Au-S键形成共价固定在一个金电极表面的寡核苷酸探针组成的双基因传感器用于同时测定两个不同的寡核苷酸靶标。一种探针,在其5'端装饰有二茂铁(SH-ssDNA-Fc),与cDNA互补,该cDNA代表编码H5N1病毒H5血凝素部分的序列。第二个探针在其5'末端装饰有亚甲蓝(SH-ssDNA-MB),与代表同一病毒N1神经氨酸酶片段的cDNA互补。用Osteryoung方波伏安法(OSWV)证实了金电极表面上两种探针的存在。杂交过程之前和之后,两种氧化还原活性复合物的氧化还原活性的变化均用作分析信号。在存在40 nM ssDNA作为SH-ssDNA-Fc探针的靶标的情况下,观察到+400±2 mV的峰。该峰随目标ssDNA浓度的增加而增加。它指示分析信号生成的“信号开启”模式。 SH-ssDNA-MB探针的特征-250±4 mV处的峰随着互补ssDNA靶标浓度从8 nM的增加而减小。这表明根据“信号关闭”模式产生了电化学信号。所提出的双基因传感器能够同时,特异性和良好的灵敏度,探测编码流感病毒两个主要​​标记物血凝素和神经氨酸酶基因的序列。

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