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首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Effects of free patchy ends in ssDNA and dsDNA on gold nanoparticles in a colorimetric gene sensor for Hepatitis C virus RNA
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Effects of free patchy ends in ssDNA and dsDNA on gold nanoparticles in a colorimetric gene sensor for Hepatitis C virus RNA

机译:在丙型肝炎病毒RNA的比色基因传感器中SSDNA和DSDNA在SSDNA和DSDNA上的影响

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The presence or absence and nature of the free patchy ends in DNA sequences has a decisive effect on the performance of colorimetric sensors based on the use of gold nanoparticles (Au NPs). The authors have designed two unmodified gene probes (probe 1: a 19-mer; probe 2: an 18-mer). They are complementary to either half of a 37-mer target derived from the conserved region of Hepatitis C Virus (HCV) RNA. Each probe has further been modified with 10-mer poly(A) and thiol-functionalized 10-mer poly(A) at the 5 positions. Nine combinations of probe and HCV RNA were then designed to investigate the effect of free patchy ends on the stability of citrate-modified Au NPs against salt-induced aggregation which lead to color change from red to blue. The aggregation of Au NPs can be monitored by ratiometric spectroscopy at wavelengths of 520 and 700nm. The differentiation between HCV RNA and control has also been studied by varying the concentration of probe and analyte. The particle size and zeta potentials were determined before and after aggregation. It is demonstrated that the change in surface charge density of the Au NPs governs the critical coagulation concentration of NaCl. The method presented here can be used to quantify HCV RNA in the 370nM to 3 mu M concentration range, and the detection limit is 500nM. The results obtained with Au NPs that are chemically non-conjugated with the oligonucleotides have been found to be valuable in rationally devising the design rules for rapid and efficient colorimetric sensing of oligonucleotides.
机译:在DNA序列中自由斑块的末端的存在或不存在性和性质对基于金纳米颗粒(Au NPS)的比色传感器的性能具有决定性影响。作者设计了两个未修改的基因探针(探针1:a 19-mer;探针2:18-mer)。它们与来自丙型肝炎病毒(HCV)RNA的保守区域的37分靶的一半互补。在5个位置,每次探针进一步用10-MEL聚(a)和硫醇官能化的10-mer聚(a)改性。然后设计探针和HCV RNA的9种组合,以研究自由蛋白端末端对柠檬酸盐改性的Au nps对盐诱导的聚集的稳定性的影响,这导致从红色变为蓝色的颜色变化。可以在波长为520和700nm的波长的比率光谱来监测Au NP的聚合。通过改变探针和分析物的浓度,还研究了HCV RNA和对照之间的分化。在聚集之前和之后确定粒度和ζ电位。证明Au NPS的表面电荷密度的变化控制了NaCl的临界凝血浓度。此处呈现的方法可用于量化在370nm至3μm浓度范围内的HCV RNA,并且检测限为500nm。已经发现用与寡核苷酸化学不缀合的Au nP获得的结果是有价值的,合理设计用于寡核苷酸的快速和高效的比色感测的设计规则。

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