Protein-responsive rolling circle amplification as a tandem template to drive amplified transduction of fluorescence signal probes for highly sensitive immunoassay

被引:40
|
作者
Yang, Wenting [1 ]
Shen, Yu [1 ]
Zhang, Danyang [1 ]
Xu, Wenju [1 ]
机构
[1] Southwest Univ, Sch Chem & Chem Engn, Minist Educ, Key Lab Luminescent & Real Time Analyt Chem, Chongqing 400715, Peoples R China
基金
中国国家自然科学基金;
关键词
DNA STRAND DISPLACEMENT; HELIX MOLECULAR SWITCH; PROXIMITY LIGATION; NUCLEIC-ACIDS; ULTRASENSITIVE DETECTION; SENSING PLATFORM; CANCER; BIOSENSOR; NANOMACHINE; TELOMERASE;
D O I
10.1039/c8cc04395g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Proximity binding-induced DNA assemblies possessing outstanding flexibility and diversity can provide great accessibility for output translation of amplifiable DNA probes or directly detectable signals. Based on a novel protein-responsive DNA assembly constructed via proximity binding-initiated rolling circle amplification (RCA), we present a sensitive and specific fluorescence resonance energy transfer (FRET) strategy for the immunoassay of mucin 1 (MUC1). The resultant RCA product containing numerous and continuous repeats as the tandem template accelerates the transduction of signal probes through the disassembly of triple-helix stem structure (THSS), achieving a significantly amplified FRET signal readout.
引用
收藏
页码:10195 / 10198
页数:4
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