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

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

Analytica chimica acta (2012-04-10)
Ruimin Li, Cen Xiong, Zhiyou Xiao, Liansheng Ling
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.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Cholesterol Oxidase from microorganisms, lyophilized powder, ≥50 units/mg protein, recombinant, expressed in E. coli
Sigma-Aldrich
Cholesterol Oxidase from microorganisms, aqueous solution, ≥30 units/mg protein (biuret)
Sigma-Aldrich
Cholesterol Oxidase from Streptomyces sp., lyophilized powder, ≥20 units/mg protein
Sigma-Aldrich
Cholesterol Oxidase microbial, recombinant, lyophilized powder, ≥10 units/mg protein