Label-free triple-helix aptamer as sensing platform for "signal-on" fluorescent detection of thrombin

被引:30
|
作者
Xu, Nan [1 ]
Wang, Quanbo [1 ]
Lei, Jianping [1 ]
Liu, Lin [1 ]
Ju, Huangxian [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210093, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Triple-helix aptamer; label-free; fluorescent detection; graphene oxide; thrombin; IN-VITRO; NUCLEIC-ACID; DNA; COMPLEX; APTASENSOR; BIOSENSOR; AMPLIFICATION; BEACONS; DESIGN; PROBE;
D O I
10.1016/j.talanta.2014.09.031
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The design of a label-free aptamer for separation of recognition sequence from signal reporter is significant to ensure the high-efficiency affinity between aptamer and target. This work develops a label-free triple-helix aptamer (THA) as sensing platform for "signal-on" fluorescent detection of thrombin. THA was composed of aptamer sequence and help DNA 1 (H1), which contained the complementary sequence of hexachloro-fluorescein (HEX) labeled help DNA 2 (H2). The specific recognition event between aptamer and thrombin triggered the dismission of THA to release H1. The released H1 then reacted with the signal probe of H2/graphene oxide (GO) nanocomposite to form H1-H2 duplex, leading to the fluorescence recovery of H2 due to the detachment of Hl-H2 duplex from the surface of GO. With employment of THA as a signal transducer and GO as a "superquencher", this method shows a sensitive response to thrombin with a wide concentration range from 5 to 1200 nM. The limit of detection is 1.8 nM (S/N =3) with excellent selectivity. Considering the universality of THA, the proposed aptasensor would provide a platform for homogeneous fluorescent detection of a wide range of analytes. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:387 / 391
页数:5
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