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点亮用于生物传感的RNA切割脱氧核酶

Lighting Up RNA-Cleaving DNAzymes for Biosensing.

作者信息

Tram Kha, Kanda Pushpinder, Li Yingfu

机构信息

Departments of Biochemistry and Biomedical Sciences and Chemistry and Chemical Biology, Michael G. DeGroote Institute for Infectious Disease Research, McMaster University, 1280 Main Street West, Hamilton, ON, Canada L8S 4K1.

出版信息

J Nucleic Acids. 2012;2012:958683. doi: 10.1155/2012/958683. Epub 2012 Nov 8.

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.

摘要

体外筛选技术的发展使得从随机序列库中分离出功能性核酸成为可能,其中包括催化性DNA分子(DNA酶)。1994年通过该技术获得的首个催化性DNA是一种可切割RNA的DNA酶。从那时起,多项体外筛选研究报告了许多其他类似核糖核酸酶的DNA酶。各种核糖核酸酶DNA酶的发现反过来又激发了人们对这些酶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。在过去十年中受到相当多关注的一个特定研究课题是将核糖核酸酶DNA酶开发成用于生物传感应用的荧光报告分子。本文简要概述了该研究课题中最重要的成果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff8e/3503364/0e1b46c6d105/JNA2012-958683.001.jpg

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