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Label-free and sensitive detection of coralyne and heparin based on target-induced G-quadruplex formation

机译:基于靶标诱导的G-四链体形成的无标记和灵敏的珊瑚和肝素检测

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Herein we propose a label-free and sensitive detection method for coralyne and heparin, based on utilizing the complex of adenosine16 (A16) and coralyne to induce the formation of a G-quadruplex scaffold. In the present work, two specific oligonucleotide strands were designed. Upon addition of coralyne, the two oligonucleotide strands formed a double chain through A2–coralyne–A2 coordination, which induced the formation of an intermolecular G-quadruplex accompanied by the proximity of two G-rich sequences. An increase in system fluorescence was observed after the addition of N-methylmorpholine (NMM). In the presence of heparin, the formation of the heparin–coralyne complex caused coralyne to be removed from the A16–coralyne complex, leading to a weaker fluorescence output. At optimal concentrations, a linear coralyne response could be observed from 0.01–5 μM and the detection limit was estimated to be 5.8 nM. The detection limit of the heparin probe was as low as 1 nM, with a linear range from 1–100 nM. Overall, this study offers a sensitive and practical assay for coralyne and heparin detection.
机译:在此,我们基于腺苷16(A16)和珊瑚蛋白的复合物诱导G-四链体支架的形成,提出了一种针对珊瑚蛋白和肝素的无标记且灵敏的检测方法。在本工作中,设计了两条特定的寡核苷酸链。加入珊瑚素后,两条寡核苷酸链通过A2-珊瑚素-A2配位形成一条双链,从而诱导了分子间G-四链体的形成,并伴随着两​​个富含G的序列的接近。加入N-甲基吗啉(NMM)后观察到系统荧光增加。在肝素的存在下,肝素-珊瑚炔复合物的形成导致珊瑚素从A16-珊瑚炔复合物中被去除,导致荧光输出减弱。在最佳浓度下,可以观察到0.01–5μM的线性珊瑚反应,检测极限估计为5.8 nM。肝素探针的检出限低至1 nM,线性范围为1–100 nM。总的来说,这项研究为珊瑚和肝素的检测提供了一种灵敏而实用的检测方法。

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