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基于分子信标的连接探针,通过真正的靶触发酶循环扩增,实现高效的核酸检测。

Molecular beacon-based junction probes for efficient detection of nucleic acids via a true target-triggered enzymatic recycling amplification.

出版信息

Anal Chem. 2011 Jan 1;83(1):14-7. doi: 10.1021/ac1025072. Epub 2010 Nov 30.

Abstract

This work reports the development of a new molecular beacon-based junction sensing system with highly sensitive DNA detection and a strong capability to identify SNPs. The single linear probe typically labels the midsection of the oligonucleotide, but our next-generation junction sensing system uses a hairpin-structured MB with labels on each end of the oligonucleotide to maintain the cleaving activity of our newly designed ssDNA-cleaved endonuclease, Nt.BbvCI, rather than the typical dsDNA-cleaved endonuclease. These design improvements guarantee a true and efficient target-triggered enzymatic recycling amplification process in our sensing system. They also afford a faster and more sensitive response toward target DNA than the first-generation junction sensing system.

摘要

本工作报道了一种新的分子信标基于连接点传感系统的开发,该系统具有高灵敏度的 DNA 检测和强大的单核苷酸多态性(SNP)识别能力。传统的线性探针通常标记寡核苷酸的中段,而我们的新一代连接点传感系统使用带有寡核苷酸两端标记的发夹结构的分子信标,以维持我们新设计的单链 DNA 切割内切酶 Nt.BbvCI 的切割活性,而不是典型的双链 DNA 切割内切酶。这些设计改进保证了传感系统中真正有效的靶标触发酶循环扩增过程。与第一代连接点传感系统相比,它们还提供了更快、更灵敏的靶 DNA 响应。

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