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用于一步法定量测量生物样品中人脱嘌呤/脱嘧啶核酸内切酶 1 活性的单分子化学修饰 DNA 荧光探针。

Unimolecular Chemically Modified DNA Fluorescent Probe for One-Step Quantitative Measurement of the Activity of Human Apurinic/Apyrimidinic Endonuclease 1 in Biological Samples.

机构信息

Beijing National Laboratory for Molecular Sciences, MOE Key Laboratory of Bioorganic Chemistry and Molecular Engineering, College of Chemistry and Molecular Engineering, Peking University , Beijing 100871, China.

出版信息

Anal Chem. 2015 Dec 15;87(24):11952-6. doi: 10.1021/acs.analchem.5b03939. Epub 2015 Nov 25.

Abstract

A novel DNA structure containing a 3' internal-loop modified abasic site has been constructed which enables effective differentiation between apurinic/apyrimidinic endonuclease (APE1) and nonspecific endonuclease (DNase I). When this unique substrate structure is employed, a double-loop frayed-end chimeric fluorescent probe is successfully developed for quantitative measurement of the activity of APE1 in biological samples without the need of additional cleanup or preconcentration steps. The method is simple and rapid and has a single-step with a linear working range between 0.1 and 5.0 U/mL and a lower limit of detection of 0.1 U/mL. It holds great potential in real-time monitoring of the variation of intracellular and extracellular APE1, which will be very useful for further understanding of the DNA repair pathways in different organisms.

摘要

已构建了一种含有 3' 内部环修饰的无碱基位点的新型 DNA 结构,该结构可有效区分脱嘌呤/脱嘧啶核酸内切酶 (APE1) 和非特异性核酸内切酶 (DNase I)。当使用这种独特的底物结构时,成功开发了一种双环磨损末端嵌合荧光探针,可定量测量生物样品中 APE1 的活性,而无需额外的清洗或预浓缩步骤。该方法简单快速,具有单步线性工作范围在 0.1 和 5.0 U/mL 之间,检测限低至 0.1 U/mL。它在实时监测细胞内和细胞外 APE1 的变化方面具有巨大潜力,这对于进一步了解不同生物体中的 DNA 修复途径将非常有用。

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