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Lighting Up RNA-Cleaving DNAzymes for Biosensing

机译:点亮切割RNA的DNA酶以进行生物传感

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摘要

The development of the in vitro selection technique has allowed the isolation of functional nucleic acids, including catalytic DNA molecules (DNAzymes), from random-sequence pools. The first-ever catalytic DNA obtained by this technique in 1994 is a DNAzyme that cleaves RNA. Since then, many other RNase-like DNAzymes have been reported from multiple in vitro selection studies. The discovery of various RNase DNAzymes has in turn stimulated the exploration of these enzymatic species for innovative applications in many different areas of research, including therapeutics, biosensing, and DNA nanotechnology. One particular research topic that has received considerable attention for the past decade is the development of RNase DNAzymes into fluorescent reporters for biosensing applications. This paper provides a concise survey of the most significant achievements within this research topic.
机译:体外选择技术的发展已允许从随机序列库中分离出功能性核酸,包括催化性DNA分子(DNA酶)。 1994年通过此技术获得的第一个催化DNA是切割RNA的DNA酶。从那时起,从多个体外选择研究中已经报道了许多其他的RNase样DNA酶。各种RNase DNA酶的发现反过来刺激了对这些酶物种的探索,以在许多不同领域的研究中进行创新应用,包括治疗,生物传感和DNA纳米技术。在过去的十年中,受到广泛关注的一个特殊研究主题是将RNase DNA酶发展为用于生物传感应用的荧光报告基因。本文对本研究主题中最重要的成就进行了简要概述。

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