Aptamer/thrombin/aptamer-AuNPs sandwich enhanced surface plasmon resonance sensor for the detection of subnanomolar thrombin

被引:149
作者
Bai, Yunfeng [1 ,2 ]
Feng, Feng [1 ,2 ]
Zhao, Lu [2 ]
Wang, Chunyu [2 ]
Wang, Haiyan [2 ]
Tian, Maozhong [2 ]
Qin, Jun [2 ]
Duan, Yali [1 ]
He, Xiaoxiao [3 ]
机构
[1] Shanxi Normal Univ, Sch Chem & Mat Sci, Linfen 041004, Peoples R China
[2] Shanxi Datong Univ, Coll Chem & Chem Engn, Datong 037009, Peoples R China
[3] Hunan Univ, State Key Lab Chemo Biosensing & Chemometr, Coll Biol, Changsha 410082, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Surface plasmon resonance; Aptamer; Thrombin; Gold nanoparticles; Sandwich assay; AMPLIFIED ELECTROCHEMICAL APTASENSOR; ULTRASENSITIVE DETECTION; AU NANOPARTICLES; LABEL-FREE; IN-VITRO; APTAMER; BIOSENSOR; SELECTION; ASSAY; BIND;
D O I
10.1016/j.bios.2013.02.004
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
A sensitive and selective aptamer/thrombin/aptamer-AuNPs sandwich enhanced surface plasmon resonance (SPR) sensor has been developed for real-time detection of subnanomolar thrombin. In this protocol, one thiol-modified thrombin aptamer (TBA29) was immobilized on gold nanoparticles (AuNPs) via Au-S bonding. The other biotinylated thrombin aptamer (TBA15) was grafted onto streptavidin pretreated SPR gold film through biotin-streptavidin recognition. The presence of thrombin would then induce the formation of a double aptamer sandwich structure on the SPR gold film and results in obvious enhancement of SPR signal, which was proportional to the concentration of thrombin. This proposed assay took advantage of sandwich binding of two affinity aptamers for increased specificity, AuNPs for signal enhancement, as well as SPR signal readout for real-time detection. The SPR signal had a good linear relationship with thrombin concentration in the range of 0.1-75 nM, and the detection limit for thrombin was determined to be as low as 0.1 nM. It was found that aptamer functionalized AuNPs enhanced the signal of SPR response and thus increased the limit of detection 4-fold and 5-fold compared to direct detection format without AuNPs. This sensor also showed good selectivity for thrombin without being affected by some other proteins, such as BSA and lysozyme. Furthermore, this proposed SPR sensing platform was successfully applied to thrombin analysis in diluted human serum samples. (C) 2013 Published by Elsevier B.V.
引用
收藏
页码:265 / 270
页数:6
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