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Improved DNA microarray detection sensitivity through immobilization of preformed in solution streptavidin/biotinylated oligonucleotide conjugates

机译:通过固定在溶液中的链霉亲和素/生物素化寡核苷酸偶联物中固定的预成型品,提高了DNA芯片检测灵敏度

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摘要

A novel immobilization approach involving binding of preformed streptavidin/biotinylated oligonucleotide conjugates onto surfaces coated with biotinylated bovine serum albumin is presented. Microarrays prepared according to the proposed method were compared, in terms of detection sensitivity and specificity, with other immobilization schemes employing coupling of biotinylated oligonucleotides onto directly adsorbed surface streptavidin, or sequential coupling of streptavidin and biotinylated oligonucleotides onto a layer of adsorbed biotinylated bovine serum albumin. A comparison was performed employing biotinylated oligonucleotides corresponding to wild- and mutant-type sequences of seven single point mutations of the BRCA1 gene. With respect to the other immobilization protocols, the proposed oligonucleotide immobilization approach offered the highest hybridization signals (at least 5 times higher) and permitted more elaborative washings, thus providing considerably higher discrimination between complimentary and non-complementary DNA sequences for all mutations tested. In addition, the hybridization kinetics were significantly enhanced compared to two other immobilization protocols, permitting PCR sample analysis in less than 40 min. Thus, the proposed oligonucleotide immobilization approach offered improved detection sensitivity and discrimination ability along with considerably reduced analysis time, and it is expected to find wide application in DNA mutation detection. (C) 2015 Elsevier B.V. All rights reserved.
机译:提出了一种新颖的固定化方法,该方法涉及将预先形成的链霉亲和素/生物素化的寡核苷酸偶联物结合到涂有生物素化的牛血清白蛋白的表面上。在检测灵敏度和特异性方面,将根据提出的方法制备的微阵列与其他固定方案进行了比较,这些固定方案采用将生物素化的寡核苷酸偶联到直接吸附的表面链霉亲和素上,或将链霉亲和素和生物素化的寡核苷酸顺序偶联到吸附的生物素化的牛血清白蛋白层上。使用对应于BRCA1基因的七个单点突变的野生型和突变型序列的生物素化寡核苷酸进行了比较。关于其他固定方案,所提出的寡核苷酸固定方法可提供最高的杂交信号(至少高5倍),并允许进行更精细的洗涤,因此可对所有测试突变的互补和非互补DNA序列提供更高的区分度。此外,与其他两种固定方案相比,杂交动力学得到了显着增强,从而可以在不到40分钟的时间内进行PCR样品分析。因此,提出的寡核苷酸固定化方法提供了改进的检测灵敏度和判别能力,同时大大缩短了分析时间,并且有望在DNA突变检测中找到广泛的应用。 (C)2015 Elsevier B.V.保留所有权利。

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