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基于 G-四链体 DNA 酶和 ABTS2-的胆固醇比色检测。

Colorimetric detection of cholesterol with G-quadruplex-based DNAzymes and ABTS2-.

机构信息

School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou, PR China.

出版信息

Anal Chim Acta. 2012 Apr 29;724:80-5. doi: 10.1016/j.aca.2012.02.015. Epub 2012 Feb 27.

Abstract

A novel colorimetric method for detection of cholesterol was developed with hemin-G-quadruplex DNAzyme by transducing oxidation of cholesterol into the color change of 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS(2-)). Oligonucleotide 5'-GTGGGTAGGGCGGGTTGG-3' (Oligo-1) formed G-quadruplex structure in the presence of K(+), it acted as a horseradish peroxidase (HRP) mimicking DNAzyme when binding hemin and catalyzed the oxidation of colorless ABTS(2-) to green ABTS(·-) by H(2)O(2), which was produced by the reaction of cholesterol and oxygen that catalyzed by cholesterol oxidase. Therefore, the oxidation of cholesterol could be transduced into the color change of ABTS(2-) by combining these two reactions. Under the optimum conditions, the absorbance was proportional to the concentration of cholesterol over the range of 1.0-30 μM, with a linear regression equation of A=0.362+0.0256C (C: μM, R=0.998) and a detection limit of 0.10 μM (3σ/slope). Moreover, the practicability of the assay in the detection of cholesterol in human serum was studied as well.

摘要

开发了一种基于血红素-G-四链体 DNA 酶的胆固醇比色检测新方法,通过将胆固醇的氧化转化为 2,2'-联氮双(3-乙基苯并噻唑啉-6-磺酸)二铵盐(ABTS(2-))的颜色变化来实现。寡核苷酸 5'-GTGGGTAGGGCGGGTTGG-3'(Oligo-1)在 K(+)存在下形成 G-四链体结构,当与血红素结合时,它充当辣根过氧化物酶(HRP)模拟 DNA 酶,并通过 H(2)O(2)催化无色 ABTS(2-)氧化为绿色 ABTS(·-),H(2)O(2)是由胆固醇氧化酶催化胆固醇和氧气反应生成的。因此,通过结合这两个反应,可以将胆固醇的氧化转化为 ABTS(2-)的颜色变化。在最佳条件下,吸光度与胆固醇浓度在 1.0-30 μM 范围内呈正比,线性回归方程为 A=0.362+0.0256C(C:μM,R=0.998),检测限为 0.10 μM(3σ/斜率)。此外,还研究了该测定法在人血清中胆固醇检测中的实用性。

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