Liu Xingti, Xue Qingwang, Ding Yongshun, Zhu Jing, Wang Lei, Jiang Wei
Key Laboratory for Colloid and Interface Chemistry of Education Ministry, Department of Chemistry, Shandong University, Jinan, 250100, P. R. China.
Analyst. 2014 Jun 7;139(11):2884-9. doi: 10.1039/c4an00389f.
A sensitive and label-free fluorescence assay for DNA detection has been developed based on cascade signal amplification combining exonuclease III (Exo III)-catalyzed recycling with rolling circle amplification. In this assay, probe DNA hybridized with template DNA was coupled onto magnetic nanoparticles to prepare a magnetic bead-probe (MNB-probe)-template complex. The complex could hybridize with the target DNA, which transformed the protruding 3' terminus of template DNA into a blunt end. Exo III could then digest template DNA, liberating the MNB-probe and target DNA. The intact target DNA then hybridized with other templates and released more MNB-probes. The liberated MNB-probe captured the primer, circular DNA and then initiated the rolling circle amplification (RCA) reaction, realizing a cascade signal amplification. Using this cascade amplification strategy, a sensitive DNA detection method was developed which was superior to many existing Exo III-based signal amplification methods. Moreover, N-methyl mesoporphyrin IX, which had a pronounced structural selectivity for the G-quadruplex, was used to combine with the G-quadruplex RCA products and generate a fluorescence signal, avoiding the need for any fluorophore-label probes. The spike and recovery experiments in a human serum sample indicated that our assay also had great potential for DNA detection in real biological samples.
基于核酸外切酶III(Exo III)催化的循环与滚环扩增相结合的级联信号放大技术,开发了一种用于DNA检测的灵敏且无标记的荧光检测方法。在该检测方法中,与模板DNA杂交的探针DNA被偶联到磁性纳米颗粒上,以制备磁珠-探针(MNB-探针)-模板复合物。该复合物可与靶DNA杂交,将模板DNA突出的3'末端转化为平端。然后Exo III可消化模板DNA,释放出MNB-探针和靶DNA。完整的靶DNA随后与其他模板杂交并释放更多的MNB-探针。释放的MNB-探针捕获引物、环状DNA,然后启动滚环扩增(RCA)反应,实现级联信号放大。利用这种级联扩增策略,开发了一种灵敏的DNA检测方法,该方法优于许多现有的基于Exo III的信号放大方法。此外,对G-四链体具有明显结构选择性的N-甲基中卟啉IX被用于与G-四链体RCA产物结合并产生荧光信号,无需任何荧光团标记的探针。在人血清样本中的加标回收实验表明,我们的检测方法在实际生物样本中的DNA检测方面也具有巨大潜力。