| Literature DB >> 24607618 |
Jia-Cheng Wang1, Yong-Sheng Wang2, Jin-Hua Xue3, Bin Zhou3, Qiu-Mei Qian3, Yong-Song Wang3, Ji-Cheng Yin3, Hui Zhao3, Hui Liu3, Shan-Du Liu3.
Abstract
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 90.8pM to 14.1nM with a detection limit of 27.3pM, 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.Entities:
Keywords: 8-hydroxy-2′-deoxyguanosine; Aptamer; Conformational switching; Gold nanoparticles; Resonance light scattering; Ultrasensitive assay
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Year: 2014 PMID: 24607618 DOI: 10.1016/j.bios.2014.02.047
Source DB: PubMed Journal: Biosens Bioelectron ISSN: 0956-5663 Impact factor: 10.618