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核酸内切酶
化学
DNA
荧光
分子生物学
DNA-(无嘌呤或无嘧啶位点)裂解酶
生物化学
生物物理学
DNA损伤
检出限
色谱法
生物
量子力学
物理
作者
Simin Fang,Lu Chen,Meiping Zhao
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2015-11-24
卷期号:87 (24): 11952-11956
被引量:54
标识
DOI:10.1021/acs.analchem.5b03939
摘要
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.
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