College of Biology, State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, China.
Talanta. 2013 Nov 15;116:330-4. doi: 10.1016/j.talanta.2013.05.021. Epub 2013 May 30.
We design a long-tail shaped DNA probe for the label-free, isothermal and sensitive detection of nucleic acids based on cycled strand displacement amplification (Ltail-CSDA). The long-tail probe, a stem-loop structure with a long poly(T) tail at 5'-termini, integrates target-binding and amplification and signaling within one multifunctional design. The specific binding between the long-tail probe and the target triggers a polymerization reaction, during which a long dsDNA product is synthesized and the hybridized target is displaced by the strand displacement activity of polymerase. The displaced target forms another specific probe-target binding and prompts cycled polymerization reactions. The proposed Ltail-CSDA has the distinct advantages of its isothermal nature, free-label, simplicity and attomolar sensitivity compared with other existing technologies. More significantly, the dynamic range of the method is extremely large, covering nine orders of magnitude. Using total RNA samples extracted from hepatitis C virus (HCV) as targets, we further demonstrate the detection capability of the method for complex nucleic acid samples, indicating its potential applicability for clinic molecular diagnostic assays.
我们设计了一种长尾状 DNA 探针,用于基于循环链置换扩增(Ltail-CSDA)的无标记、等温、灵敏的核酸检测。长尾探针是一种茎环结构,5'-末端带有长的聚(T)尾巴,将靶标结合、扩增和信号转导集成在一个多功能设计中。长尾探针与靶标的特异性结合触发聚合反应,在此过程中合成长的 dsDNA 产物,并且聚合酶的链置换活性将杂交的靶标置换。被置换的靶标形成另一个特异性探针-靶标结合,并促使循环聚合反应。与其他现有技术相比,所提出的 Ltail-CSDA 具有等温性质、无标记、简单和纳摩尔灵敏度的独特优势。更重要的是,该方法的动态范围非常大,涵盖了 9 个数量级。我们使用从丙型肝炎病毒(HCV)中提取的总 RNA 样本作为靶标,进一步证明了该方法对复杂核酸样本的检测能力,表明其在临床分子诊断中的潜在适用性。