Biological investigation using a shear horizontal surface acoustic wave sensor: small "click generated" DNA hybridization detection.

Biosensors & bioelectronics Pub Date : 2010-12-15 Epub Date: 2010-08-19 DOI:10.1016/j.bios.2010.08.036
Chouki Zerrouki, Najla Fourati, Romain Lucas, Julien Vergnaud, Jean-Marie Fougnion, Rachida Zerrouki, Christine Pernelle
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引用次数: 17

Abstract

We have used a 104 MHz lithium tantalate (LiTaO(3)) surface acoustic wave (SAW) sensor to investigate DNA probes grafting and their further hybridization with natural and click generated (Cg-DNA) oligonucleotides. Natural DNA targets of different strand lengths, tosyl-di(tri, tetra) thymidine and azido-di(tri, tetra) thymidine oligonucleotides were tested. In our case, and besides the follow-up of a 34mer DNA hybridization, we detected complementarity between natural DNA probes and azido-tetra-thymidine for the first time, whereas previous hybridization studies reported a minimal of 10-mer oligonucleotides recognition length. We also demonstrated that contrarily to natural DNA, the synthesized oligonucleotides present stable bonds with complementary DNA strands. Frequency responses of both grafting and hybridization have shown the same shape: an exponential decay with different time constants, (187±1)s and (68±19) s for grafting and hybridization respectively. We have also shown that recognition between DNA strands and tetranucleotide analogues is comparable to natural 34mer DNA bases and presents the same time constant within uncertainties.

生物学研究用剪切水平表面声波传感器:小“点击产生”DNA杂交检测。
我们使用104 MHz钽酸锂(LiTaO(3))表面声波(SAW)传感器来研究DNA探针的接枝及其与天然和点击生成(gc -DNA)寡核苷酸的进一步杂交。测定了不同链长的天然DNA靶标、toyl -di(三,四)胸腺嘧啶和叠氮-di(三,四)胸腺嘧啶寡核苷酸。在我们的案例中,除了后续的34mer DNA杂交之外,我们首次检测到天然DNA探针与叠氮四胸腺嘧啶之间的互补性,而之前的杂交研究报道了最小的10-mer寡核苷酸识别长度。我们还证明,与天然DNA相反,合成的寡核苷酸与互补DNA链呈现稳定的键。接枝和杂化的频率响应都表现出相同的形状:不同时间常数的指数衰减,接枝和杂化分别为(187±1)s和(68±19)s。我们还表明,DNA链和四核苷酸类似物之间的识别与天然34聚体DNA碱基相当,并且在不确定度内呈现相同的时间常数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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