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Femtomolar oligonucleotide detection by a one-step gold nanoparticle-based assay

机译:通过一步式金纳米粒子检测技术检测飞沫寡核苷酸

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摘要

A sequence-specific oligonucleotide detection method based on the tail-to-tail aggregation of functionalized gold nanoparticles in the presence of target analytes is presented together with its optimization and capabilities for detection of single nucleotide polymorphisms (SNPs). In this single-step method, capture probes are freely accessible for hybridization, resulting in an improved assay performance compared to substrate-based assays. The analytes bring the nanoparticles close to each other via hybridization, causing a red shift of the nanoparticle plasmon peak detected by a spectrophotometer or CCD camera coupled to a darkfield imaging system. Optimal conditions for the assay were found to be (i) use of capture probes complementary to the target without any gap, (ii) maximum possible probe density on the gold nanoparticles, and (iii) 1 M ionic strength buffer. The optimized assay has a 1 fM limit of detection and fM to 10 pM dynamic range, with detection of perfect match sequences being three orders of magnitude more sensitive than targets with single nucleotide mismatches. (C) 2015 Elsevier B.V. All rights reserved.
机译:提出了一种序列特异性寡核苷酸检测方法,该方法基于目标分析物存在下功能化金纳米颗粒的尾到尾聚集,以及其优化和检测单核苷酸多态性(SNP)的能力。在这种单步方法中,捕获探针可自由接近进行杂交,与基于底物的测定相比,可提高测定性能。分析物通过杂交使纳米颗粒彼此靠近,从而导致由耦合到暗场成像系统的分光光度计或CCD摄像机检测到的纳米颗粒等离子体激元峰发生红移。发现测定的最佳条件是(i)使用与靶互补的捕获探针而没有任何间隙;(ii)金纳米颗粒上的最大可能探针密度;以及(iii)1M离子强度缓冲液。优化的检测方法的检测极限为1 fM,动态范围为fM至10 pM,完美匹配序列的检测灵敏度比单核苷酸错配的靶标高三个数量级。 (C)2015 Elsevier B.V.保留所有权利。

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