Assembly of DNA Probes into Superstructures for Dramatically Enhancing Enzymatic Stability and Signal-to-Background Ratio

被引:10
|
作者
Wang, Fengchao [1 ,2 ]
Li, Qiang [1 ,2 ]
Zhang, Pengjuan [1 ,2 ]
Liu, Xuehui [1 ,2 ]
Li, Ang [3 ]
Yang, Jie [1 ,2 ]
Liu, Dingbin [1 ,2 ,3 ,4 ]
机构
[1] Nankai Univ, Coll Chem, Res Ctr Analyt Sci, Tianjin 300071, Peoples R China
[2] Nankai Univ, Tianjin Key Lab Mol Recognit & Biosensing, Tianjin 300071, Peoples R China
[3] Nankai Univ, State Key Lab Med Chem Biol, Tianjin 300071, Peoples R China
[4] Collaborat Innovat Ctr Chem Sci & Engn, Tianjin 300071, Peoples R China
来源
ACS SENSORS | 2018年 / 3卷 / 12期
基金
中国国家自然科学基金;
关键词
DNA probes; biological detection; assembly; gold nanoparticles; enhanced enzyme resistance; MESSENGER-RNA DETECTION; NANO-FLARES;
D O I
10.1021/acssensors.8b01247
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
DNA fluorescent probes are versatile tools that are widely used for biological detection in tubes. Using DNA probes in living systems, however, represents a significant challenge because of the endogenous nuclease-induced DNA degradation and strong background fluorescence in complex biological environments. Here, we show that assembling DNA probes into core-satellite gold nanoparticle (AuNP) superstructures could unprecedentedly enhance enzymatic stability and reduce background interference. The embedded DNA probes are protected from interaction with nuclease, eliminating the enzymatic degradation. In the meantime, the AuNP superstructures show extremely high quenching efficiency (>98%) toward the embedded DNA probes, whose fluorescence can be instantly turned on by the target binding, resulting in high signal-to-background ratio. To demonstrate these distinct properties, we made use of the assembled nanoprobes to monitor the ATP levels under different stimuli in living cells. The assembly strategy leads to a new opportunity for accurately sensing targets in living systems.
引用
收藏
页码:2702 / 2708
页数:13
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