State Key Laboratory of Analytical Chemistry for Life Science, Department of Chemistry, Nanjing University, Nanjing 210093, PR China.
Biosens Bioelectron. 2013 Mar 15;41:348-53. doi: 10.1016/j.bios.2012.08.050. Epub 2012 Aug 30.
A highly sensitive DNA biosensing method down to sub-femtomolar level with excellent selectivity was proposed by designing an amplified synthesis of horseradish peroxidase mimicking DNAzyme and introducing the amplified DNAzyme to chemiluminescent (CL) imaging. The amplified synthesis was achieved by combining a target DNA related ligase reaction with rolling circle amplification (RCA), which produced thousands of repeated sequences to bind hemin and form a mass of horseradish peroxidase-mimicing DNAzyme units. The amplification strategy greatly enhanced the CL emission of the luminol-H(2)O(2) system. The genotyping method displayed highly specific biochemistry in allele discrimination. The novel CL imaging strategy based on ligation-mediated RCA synthesis of DNAzyme showed high fidelity in discriminating single-base mismatch and efficiently facilitated signal amplification for sensitive target DNA detection. It could detect DNA ranging from 1×10(-15) M to 1×10(-11) M with a detection limit of 0.26 fM. The proposed approach provided a robust, cost-efficient, highly sensitive and specific platform for genetic target analysis in bioanalysis and clinic biomedical application.
提出了一种高灵敏度的 DNA 生物传感方法,可将辣根过氧化物酶模拟 DNA 酶的放大合成与化学发光(CL)成像相结合,将检测下限降低到亚 femtomolar 水平,并具有优异的选择性。通过将与靶 DNA 相关的连接酶反应与滚环扩增(RCA)相结合,实现了放大合成,产生了数千个重复序列以结合血红素并形成大量辣根过氧化物酶模拟 DNA 酶单元。该放大策略极大地增强了鲁米诺-H2O2 体系的 CL 发射。该基因分型方法在等位基因鉴别中表现出高度特异性的生物化学。基于连接介导的 DNA 酶 RCA 合成的新型 CL 成像策略在区分单碱基错配方面具有高度的保真度,并有效地促进了信号放大,从而实现了对敏感靶 DNA 的检测。它可以检测从 1×10(-15) M 到 1×10(-11) M 的 DNA,检测限为 0.26 fM。该方法为生物分析和临床生物医学应用中的遗传靶分析提供了一个强大、经济高效、高灵敏度和特异性的平台。