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基于凝血酶结合DNA适体-肽共轭物的荧光钾离子传感探针的合成

Synthesis of Fluorescent Potassium Ion-Sensing Probes Based on a Thrombin-Binding DNA Aptamer-Peptide Conjugate.

作者信息

Takenaka Shigeori

机构信息

Department of Applied Chemistry, Kyushu Institute of Technology, Kitakyushu, Japan.

出版信息

Curr Protoc Nucleic Acid Chem. 2015 Sep 1;62:8.9.1-8.9.9. doi: 10.1002/0471142700.nc0809s62.

Abstract

This unit provides a procedure for synthesis of the potassium-sensing peptide-oligodeoxyribonucleotide conjugate PSO-5 for visualizing potassium ions (K(+) ) in living cells. It is constructed by combining an oligodeoxyribonucleotide carrying a thrombin-binding DNA aptamer (TBA) sequence with an uncharged peptide carrying biotin and the fluorescence tags fluorescein (FAM) and tetramethylrhodamine (TAMRA). The PSO-5 and biotin-modified nuclear export signal peptide are conjugated through streptavidin, and this sensing molecule is introduced into the cell where it is localized in the cytoplasm. The TBA part of PSO-5 shows a conformational change from a random coil to a tetraplex structure induced by K(+) and a change in the fluorescence resonance energy transfer (FRET) efficiency between FAM and TAMRA arising from its conformational change, enabling fluorometric detection of changes in K(+) concentration.

摘要

本单元提供了一种合成钾离子感应肽 - 寡脱氧核糖核苷酸共轭物PSO - 5的方法,用于可视化活细胞中的钾离子(K⁺)。它是通过将携带凝血酶结合DNA适配体(TBA)序列的寡脱氧核糖核苷酸与携带生物素以及荧光标签荧光素(FAM)和四甲基罗丹明(TAMRA)的不带电荷的肽相结合而构建的。PSO - 5和生物素修饰的核输出信号肽通过链霉亲和素共轭,并且这种传感分子被引入细胞并定位在细胞质中。PSO - 5的TBA部分在K⁺诱导下显示出从无规卷曲到四重结构的构象变化,并且由于其构象变化导致FAM和TAMRA之间的荧光共振能量转移(FRET)效率发生变化,从而能够通过荧光法检测K⁺浓度的变化。

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