Institute of Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel.
Anal Chem. 2012 Jan 17;84(2):1042-8. doi: 10.1021/ac202643y. Epub 2011 Dec 28.
An enzyme-free amplified detection platform is described using the horseradish peroxidase (HRP)-mimicking DNAzyme as an amplifying label. Two hairpin structures that include three-fourths and one-fourth of the HRP-mimicking DNAzyme in caged, inactive configurations are used as functional elements for the amplified detection of the target DNA. In the presence of the analyte DNA, one of the hairpins is opened, and this triggers the autonomous cross-opening of the two hairpins using the strand displacement principle. This leads to the formation of nanowires consisting of the HRP-mimicking DNAzyme. The resulting DNA nanowires act as catalytic labels for the colorimetric or chemiluminescent readout of the sensing processes (the term "enzyme-free" refers to a protein-free catalyst). The analytical platform allows the sensing of the analyte DNA with a detection limit corresponding to 1 × 10(-13) M. The optimized system acts as a versatile sensing platform, and by coaddition of a "helper" hairpin structure any DNA sequence may be analyzed by the system. This is exemplified with the detection of the BRCA1 oncogene with a detection limit of 1 × 10(-13) M.
一种无酶放大检测平台,使用辣根过氧化物酶(HRP)模拟 DNA 酶作为放大标记。两个发夹结构,包括四分之三和四分之一的 HRP 模拟 DNA 酶在笼状,非活性构象中用作目标 DNA 的放大检测的功能元件。在分析物 DNA 的存在下,一个发夹被打开,这触发了两个发夹的自动交叉打开使用链置换原理。这导致纳米线的形成,包括 HRP 模拟 DNA 酶。所得的 DNA 纳米线作为用于检测过程的比色或化学发光读出的催化标记(术语“无酶”是指无蛋白催化剂)。该分析平台允许检测分析物 DNA 的检测限对应于 1×10(-13)M。优化后的系统充当多功能传感平台,并且通过共添加“辅助”发夹结构,该系统可以分析任何 DNA 序列。这通过检测 BRCA1 致癌基因的检测限为 1×10(-13)M 得到了例证。