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Facile SNP detection using bifunctional, cross-linking oligonucleotide probes

机译:使用双功能,交联寡核苷酸探针轻松检测SNP

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摘要

A facile, sensitive method for detecting specific sequences of oligonucleotides was developed. Detection of DNA sequences with single nucleotide discrimination is achieved by combining the selectivity of hybridization with an efficient cross-linking reaction. Readily synthesized bifunctional oligonucleotide probes containing a modified pyrimidine that is capable of forming interstrand cross-links under mild oxidative conditions internally, and biotin at their 5-termini were used to discriminate between 16-nt long sites in plasmid DNA that differ by a single nucleotide. The target sequence was detected via fluorescence spectroscopy by utilizing conjugates of avidin and horseradish peroxidase in a microtiter plate assay. The method is able to detect as little as 250 fmol of target without using PCR and exhibits single nucleotide discrimination that approaches 200:1. In principle, this method is capable of probing any target sequence containing a 2-deoxyadenosine.
机译:开发了一种简便,灵敏的检测寡核苷酸特定序列的方法。通过将杂交的选择性与有效的交联反应相结合,可以实现具有单核苷酸区分的DNA序列检测。使用易于合成的双功能寡核苷酸探针,该探针包含能够在温和的氧化条件下内部形成链间交联的修饰的嘧啶,并在其5末端的生物素用于区分质粒DNA中16个核苷酸长的位点,这些位点之间存在单个核苷酸差异。通过在微量滴定板测定中利用抗生物素蛋白和辣根过氧化物酶的缀合物,通过荧光光谱法检测靶序列。该方法无需使用PCR即可检测低至250 fmol的靶标,并表现出接近200:1的单核苷酸区分度。原则上,该方法能够探测包含2-脱氧腺苷的任何靶序列。

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