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使用双芘修饰的RNA探针进行RNA的固相检测。

Solid-phase detection of RNA using bispyrene-modified RNA probe.

作者信息

Sakamoto Takashi, Kobori Akio, Murakami Akira

机构信息

Department of Biomolecular Engineering, Kyoto Institute of Technology, Sakyo-ku, Kyoto 606-8585, Japan.

出版信息

Nucleic Acids Symp Ser (Oxf). 2006(50):215-6. doi: 10.1093/nass/nrl107.

Abstract

Bispyrene modified 2'-O-methyl oligoRNA (OMUpy2), which is a useful fluorescent probe for specific RNA detection, was immobilized on a glass substrate via various linker molecules to develop a more convenient RNA detection chip for gene expression study. As the fluorescence intensity of OMUpy2 enhanced greatly when it hybridized with its complementary RNA, it was expected that RNA detection by OMUpy2-immobilized chip (RNA-chip) required neither fluorescent labels to target nucleic acid nor washing protocol after the hybridization. As the linker molecules, oligo(dT), agarose, and poly(ethylene glycol) (PEG) were chosen, and the fluorescence from the chip was measured by a fluorescence microscope. Results indicated that the RNA-chip was able to detect the complementary oligoribonucleotide (cORN) without target labeling and washing protocols. Furthermore, the background emission was reduced as the length of the linker increased. In the case of PEG linker, 25-fold enhancement of the fluorescence intensity of the OMUpy2 was observed upon the addition of cORN.

摘要

双芘修饰的2'-O-甲基寡核糖核酸(OMUpy2)是一种用于特异性RNA检测的有用荧光探针,通过各种连接分子固定在玻璃基板上,以开发一种用于基因表达研究的更便捷的RNA检测芯片。由于OMUpy2与其互补RNA杂交时荧光强度大大增强,预计通过固定有OMUpy2的芯片(RNA芯片)进行RNA检测既不需要对靶核酸进行荧光标记,也不需要在杂交后进行洗涤操作。作为连接分子,选择了寡聚(dT)、琼脂糖和聚乙二醇(PEG),并通过荧光显微镜测量芯片发出的荧光。结果表明,RNA芯片能够在无需靶标标记和洗涤操作的情况下检测互补寡核糖核苷酸(cORN)。此外,随着连接分子长度的增加,背景发射降低。在使用PEG连接分子的情况下,加入cORN后观察到OMUpy2的荧光强度增强了25倍。

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