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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Multianalyte, dipstick-type, nanoparticle-based DNA biosensor for visual genotyping of single-nucleotide polymorphisms
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Multianalyte, dipstick-type, nanoparticle-based DNA biosensor for visual genotyping of single-nucleotide polymorphisms

机译:用于单核苷酸多态性视觉基因分型的多分析物,量油尺型,基于纳米颗粒的DNA生物传感器

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DNA biosensors involve molecular recognition of the target sequence by hybridization with specific probes and detection by electrochemical, optical or gravimetric transduction. Disposable, dipstick-type biosensors have been developed recently, which enable visual detection of DNA Without Using instruments. In this context, we report a multianalyte DNA biosensor for Visual genotyping of two single-nucleotide polymorphisms (SNPs). As a model, the biosensor was applied to the Simultaneous genotyping Of two SNPs, entailing the detection of four alleles. A PCR product that flanks both polymorphic sites is subjected to a single primer extension (PEXT) reaction employing four allele-specific primers, each containing a region complementary to an allele and a characteristic segment that enables subsequent capture on a test zone of the biosensor. The primers are extended with dNTPs and biotin-dUTP only if there is perfect complementarity with the interrogated sequence. The PEXT mixture is applied to the biosensor. As the developing buffer migrates along the strip, all the allele-specific primers are Captured by immobilized oligonucleotides at the four test zones of the biosensor and detected by antibiotin-functionalized gold nanoparticles. As a result, the test zones are colored red if extension has Occurred denoting the presence of the corresponding allele in the original sample. The excess nanoparticles are captured by immobilized biotinylated albumin at the control zone of the sensor forming another red zone that indicates the proper performance of the system. The assay was applied Successfully to the genotyping of twenty clinical samples for two common SNPs of MBL2 gene.
机译:DNA生物传感器涉及通过与特定探针杂交并通过电化学,光学或重量比转导检测来对靶序列进行分子识别。最近开发了一次性的量油尺型生物传感器,无需使用仪器即可目测DNA。在这种情况下,我们报告了一种用于两个单核苷酸多态性(SNP)的视觉基因分型的多分析物DNA生物传感器。作为模型,将生物传感器应用于两个SNP的同时基因分型,需要检测四个等位基因。将两个多态性位点两侧的PCR产物进行单引物延伸(PEXT)反应,该反应使用四个等位基因特异性引物,每个引物均包含一个与等位基因互补的区域和一个特征性片段,该片段可随后在生物传感器的测试区域捕获。仅当与被询问的序列具有完美的互补性时,才用dNTP和生物素-dUTP扩展引物。将PEXT混合物应用于生物传感器。随着显影缓冲液沿着条带迁移,所有等位基因特异性引物均被固定在生物传感器四个测试区域的寡核苷酸捕获,并被抗生物素功能化的金纳米颗粒检测到。结果,如果发生延伸表示原始样品中存在相应的等位基因,则测试区域将显示为红色。多余的纳米颗粒在传感器的控制区域被固定化的生物素化白蛋白捕获,形成另一个红色区域,表明系统正常运行。该测定法成功地应用于20个临床样本的MBL2基因的两个常见SNP的基因分型。

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