An ultrasensitive label-free assay of 8-hydroxy-2′-deoxyguanosine based on the conformational switching of aptamer

被引:25
作者
Wang, Jia-Cheng [1 ,2 ]
Wang, Yong-Sheng [1 ]
Xue, Jin-Hua [1 ]
Zhou, Bin [1 ]
Qian, Qiu-Mei [1 ]
Wang, Yong-Song [1 ]
Yin, Ji-Cheng [1 ]
Zhao, Hui [1 ]
Liu, Hui [1 ]
Liu, Shan-Du [1 ]
机构
[1] Univ South China, Coll Publ Hlth, Hengyang 421001, Peoples R China
[2] Dali Univ, Coll Publ Hlth, Dali 671000, Peoples R China
基金
中国国家自然科学基金;
关键词
Ultrasensitive assay; Aptamer; Gold nanoparticles; 8-hydroxy-2 '-deoxyguanosine; Conformational switching; Resonance light scattering; FUNCTIONALIZED GOLD NANOPARTICLES; OXIDATIVE DNA-DAMAGE; LIGHT-SCATTERING; COLORIMETRIC DETECTION; CANCER-PATIENTS; G-QUADRUPLEXES; SENSOR; BIOMARKER; SELECTION; CYSTEINE;
D O I
10.1016/j.bios.2014.02.047
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We developed a highly sensitive label-free assay of 8-hydroxy-2 '-deoxyguanosine (8-OHdG) using 8-OHdG-aptamer (Apt) as the recognition element. The Apt was adsorbed onto the surface of gold nanoparticles (AuNPs), which prevents them from aggregating under high-salt conditions. Upon addition of 8-OHdG, the conformation of the Apt changes to form a G-quadruplex structure, which leads to the aggregation of the AuNPs along with the increase of the resonance light scattering intensity. The mechanism of 8-OHdG that induces Apt to form G-quadruplexes structure was studied by circular dichroism. The response signals linearly correlated with the concentration of 8-OHdG ranging from 90.8 pM to 14.1 nM with a detection limit of 27.3 pM, which is much lower than that obtained by other methods. This method does not need any label steps and sophisticated equipment. The application for detection of 8-OHdG in real samples further demonstrated its reliability. This strategy would be helpful for developing a universal analytical method by simply replacing corresponding aptamers for various target molecules. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:22 / 26
页数:5
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