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Label-Free Voltammetric Detection Using Individually Addressable Oligonucleotide Microelectrode Arrays

机译:使用可单独寻址的寡核苷酸微电极阵列进行无标记伏安法检测。

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The utility and performance of label-free, oligonucleotide probes for reagentless detection of dilute target analytes was examined using a voltammetric transduction principle in an array format. Multistep, solid-state fabrication yielded preproduction arrays of 16 individually addressable, 30 (mu)m diameter microelectrodes in a 30 mm X 6.5 mm X 0.5 mm dipstick disposable device. The specificity of 16 nucleotide (nt) 2'-O-methylribonucleic acid and 22 nt DNA backbone probes bound through Mg~(2+)-phosphonate bridges to polypyrrole films on the microelectrodes were studied using microbial target RNAs of various lengths. Probe-specific interactions with Escherichia coli O157 H7 23S rRNA (2907 nt) and Candida albicans 18S rRNA (1788 nt) were detected at 65 and 58 fmol/mL, respectively, in volumes as low as 0.5 mL. Specificity studies showed that, for a given probe, "non-target" transcripts can contribute to changes in the voltammetric detection signal, though with responses that never exceed 70percent of the detection signal acquired for specifically designed complementary targets. These results statistically validate the use of the voltammetric microelectrode array for obtaining a "yes-no" answer on complementary specific binding. The study also identifies challenges and pitfalls for the selection strategies of oligonucleotide probes.
机译:使用伏安转导原理以阵列形式检查了用于无试剂检测稀释的目标分析物的无标记寡核苷酸探针的实用性和性能。通过多步固态制造,可以在30 mm X 6.5 mm X 0.5 mm量油尺一次性装置中生产16个可单独寻址,直径为30μm的微电极的预生产阵列。利用各种长度的微生物靶RNA,研究了通过Mg〜(2 +)-膦酸酯桥结合到聚吡咯膜上的16个核苷酸(nt)的2'-O-甲基核糖核酸和22个nt的DNA骨架探针的特异性。与大肠杆菌O157 H7 23S rRNA(2907 nt)和白色念珠菌18S rRNA(1788 nt)的探针特异性相互作用分别在低至0.5 mL的体积下以65和58 fmol / mL检测。特异性研究表明,对于给定的探针,“非靶标”转录本可以促进伏安法检测信号的变化,尽管其响应永远不会超过为专门设计的互补靶标而获得的检测信号的70%。这些结果从统计学上验证了伏安法微电极阵列在互补特异性结合中获得“是-否”答案的使用。该研究还确定了寡核苷酸探针选择策略的挑战和陷阱。

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