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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Preparation of novel fluorescent DNA bio-dots and their application for biothiols and glutathione reductase activity detection
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Preparation of novel fluorescent DNA bio-dots and their application for biothiols and glutathione reductase activity detection

机译:新型荧光DNA生物点的制备及其在生物硫醇和谷胱甘肽还原酶活性检测中的应用

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A new class of fluorescent bin-dots have been successfully prepared by hydrothermal treatment of polycytosine DNA at low temperature down to 80 degrees C. The inter-molecule interaction of aromatic cytosine bases forms sp(2) carbon-like centers as the luminescence centers or chromophores. In the presence of Ag+, the formation of C-Ag+-C base pairs results in the destroying of the luminescence centers and thus the fluorescence (FL) quenching of the bio-dots. However, with the addition of biothiols, Ag+ prefers to react with biothiols to form the Ag+-S bond, hence a restoration of FL emission can be observed. Moreover, by employing the classic glutathione reductase (GR) catalyzed enzymatic reaction, this concept can be readily applied to the selective quantification of oxidized glutathione (GSSG) as well as the activity of GR with a very robust, simple, and rapid procedure. It is worth looking forward to design DNAs with a specific function to prepare fluorescent bin-dots for simple biological applications. (C) 2015 Elsevier B.V. All rights reserved.
机译:通过在低至80摄氏度的低温下对多胞嘧啶DNA进行水热处理,已成功制备了新型的荧光bin-dots。芳香族胞嘧啶碱基的分子间相互作用形成sp(2)碳状中心作为发光中心或发色团。在存在Ag +的情况下,C-Ag + -C碱基对的形成导致发光中心的破坏,从而导致生物点的荧光(FL)猝灭。但是,通过添加生物硫醇,Ag +倾向于与生物硫醇反应形成Ag + -S键,因此可以观察到FL发射的恢复。此外,通过采用经典的谷胱甘肽还原酶(GR)催化的酶促反应,该概念可以很容易地应用于氧化谷胱甘肽(GSSG)的选择性定量以及GR的活性,方法非常可靠,简单且快速。值得期待的是设计具有特定功能的DNA,以制备用于简单生物学应用的荧光bin-dot。 (C)2015 Elsevier B.V.保留所有权利。

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