Nucleic acid sensing by an orthogonal reporter system based on homo-DNA.

Matthias Stoop, Camille Désiron, Christian J Leumann
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引用次数: 4

Abstract

We have developed an assay for single strand DNA or RNA detection which is based on the homo-DNA templated Staudinger reduction of the profluorophore rhodamine-azide. The assay is based on a three component system, consisting of a homo-DNA/DNA hybrid probe, a set of homo-DNA reporter strands and the target DNA or RNA. We present two different formats of the assay (Omega probe and linear probe) in which the linear probe was found to perform best with catalytic turnover of the reporter strands (TON: 8) and a match/mismatch discrimination of up to 19. The advantage of this system is that the reporting (homo-DNA) and sensing (DNA) domain are decoupled from each other since the two pairing systems are bioorthogonal. This allows independent optimization of either domain which may lead to higher selectivity in in vivo imaging.

基于同源dna的正交报告系统的核酸传感。
我们已经开发了一种检测单链DNA或RNA的方法,该方法是基于同源DNA模板化的Staudinger还原的多氟罗丹明叠氮化物。该分析是基于一个三组分系统,包括一个同源DNA/DNA杂交探针,一组同源DNA报告链和目标DNA或RNA。我们提出了两种不同的检测格式(Omega探针和线性探针),其中线性探针被发现在报告链的催化周转(TON: 8)和匹配/不匹配辨别高达19方面表现最好。该系统的优点是由于两个配对系统是生物正交的,因此报告(同源DNA)和传感(DNA)结构域彼此解耦。这允许独立优化的领域,这可能导致更高的选择性在体内成像。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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