Au-NPs enhanced SPR biosensor based on hairpin DNA without the effect of nonspecific adsorption

被引:25
作者
Luan, Qingfen [1 ]
Zhou, Kebin [1 ]
Tan, Haina [1 ]
Yang, Dan [1 ]
Yao, Xin [1 ,2 ]
机构
[1] Chinese Acad Sci, Grad Univ, Coll Chem & Chem Engn, Beijing 100049, Peoples R China
[2] Peking Univ, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
Gold nanoparticles; Hairpin DNA; Surface plasmon resonance; RsaI endonuclease; Nonspecific adsorption; SURFACE-PLASMON RESONANCE; SELF-ASSEMBLED MONOLAYERS; SEQUENCE-SPECIFIC DETECTION; ENERGY-TRANSFER ASSAY; LABEL-FREE DETECTION; MOLECULAR BEACONS; LIGASE; NANOPARTICLES; HYBRIDIZATION; SPECTROSCOPY;
D O I
10.1016/j.bios.2010.10.035
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Gold nanoparticles (Au-NPs) are usually used to amplify surface plasmon resonance (SPR) signals, however, the serious nonspecific adsorption has largely limited their practical applications. Here, we developed a novel Au-NPs enhanced biosensor without the effect of nonspecific adsorption: cutting Au-NPs off from the biosensor surface by Rsal endonuclease. In order to further improve the sensitivity, the probe DNA was designed specially. After the cleavage reaction, the residual probe DNA formed hairpin structure, which also resulted in a great change in SPR dip shift. Then, with the coaction of Au-NPs and conformation change of probe DNA, the SPR signal was amplified greatly. Using this method, we monitored the process of DNA cleavage in real-time and achieved a detection level of 5 x 10(-8) M. Moreover, the result of X-ray photoelectron spectroscopy (XPS) experiment further confirmed that large nonspecific adsorption existed. However, because SPR recorded a process in which the Au-NPs were cut off, the serious nonspecific adsorption did not affect the experimental result. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:2473 / 2477
页数:5
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