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以二茂铁基萘二酰亚胺作为四链体DNA特异性结合剂的电化学端粒酶检测法。

Electrochemical telomerase assay with ferrocenylnaphthalene diimide as a tetraplex DNA-specific binder.

作者信息

Sato Shinobu, Kondo Hiroki, Nojima Takahiko, Takenaka Shigeori

机构信息

Department of Biochemical Engineering and Science, Kyushu Institute of Technology, Iizuka, Japan.

出版信息

Anal Chem. 2005 Nov 15;77(22):7304-9. doi: 10.1021/ac0510235.

Abstract

Spectroscopic studies revealed that ferrocenylnaphthalene diimide (1) can bind to tetraplex DNA at high potassium ion concentration. The tetraplex DNA was stabilized by the binding of 1, and this effect was larger than that of any other tetraplex stabilizers, which are known as a telomerase inhibitor. Quantitative analysis with circular dichroism and a quartz crystal microbalance strongly suggested a 3:1 binding stoichiometry of 1 to the tetraplex DNA. The telomere sequence could be extended by telomerase with the telomerase substrate primer on the surface of an electrode as proven by an increased current signal of 1 bound to the tetraplex DNA formed on the electrode. This is the first example of electrochemical detection of telomerase activity without relying on PCR.

摘要

光谱研究表明,二茂铁基萘二亚胺(1)在高钾离子浓度下可与四链体DNA结合。1的结合使四链体DNA得以稳定,且这种作用比任何其他已知作为端粒酶抑制剂的四链体稳定剂都更强。圆二色光谱和石英晶体微天平的定量分析有力地表明1与四链体DNA的结合化学计量比为3:1。如电极表面结合到四链体DNA上的1的电流信号增加所证明的,端粒酶可利用电极表面的端粒酶底物引物延长端粒序列。这是首个不依赖聚合酶链式反应(PCR)进行端粒酶活性电化学检测的实例。

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