Lighting Up RNA-Cleaving DNAzymes for Biosensing.

IF 1.3 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Journal of Nucleic Acids Pub Date : 2012-01-01 Epub Date: 2012-11-08 DOI:10.1155/2012/958683
Kha Tram, Pushpinder Kanda, Yingfu Li
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引用次数: 23

Abstract

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.

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点亮用于生物传感的rna切割dna酶。
体外选择技术的发展已经允许从随机序列池中分离功能核酸,包括催化DNA分子(DNAzymes)。1994年,该技术首次获得催化DNA是一种切割RNA的DNAzyme。从那时起,许多其他类似rna的DNAzymes已经从多个体外选择研究中被报道出来。各种RNase DNAzymes的发现反过来刺激了这些酶物种在许多不同研究领域的创新应用的探索,包括治疗学,生物传感和DNA纳米技术。在过去的十年中,一个特别的研究课题是将RNase DNAzymes开发成生物传感应用的荧光报告基因。本文简要介绍了本研究课题中最重要的成果。
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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来源期刊
Journal of Nucleic Acids
Journal of Nucleic Acids BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
3.10
自引率
21.70%
发文量
5
审稿时长
12 weeks
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