A novel aptasensor strategy for protein detection based on G-quadruplex and exonuclease Ⅲ-aided recycling amplification

被引:6
作者
Huan Shi [1 ,2 ]
Tian Jin [1 ,2 ]
Jiewen Zhang [1 ]
Xiaoting Huang [1 ,2 ]
Chunyan Tan [1 ,2 ]
Yuyang Jiang [1 ,3 ]
Ying Tan [1 ,2 ]
机构
[1] State Key Laboratory of Chemical Oncogenomics, Key Laboratory of Chemical Biology, the Graduate School at Shenzhen, Tsinghua University
[2] Department of Chemistry, Tsinghua University
[3] Department of Pharmacology and Pharmaceutical Sciences, School of Medicine, Tsinghua University
关键词
Aptasensor; Exonuclease Ⅲ-aided recycling; amplification; G-quadruplex; Magnetic beads; MUC1;
D O I
暂无
中图分类号
R446 [实验室诊断]; TP212 [发送器(变换器)、传感器];
学科分类号
100208 ; 080202 ;
摘要
The detection of biomarkers is of great significance in the diagnosis of numerous diseases,especially cancer.Herein,we developed a sensitive and universal fluorescent aptasensor strategy based on magnetic beads,DNA G-quadruplex,and exonuclease III(Exo III).In the presence of a target protein,a label-free single strand DNA(ssDNA) hybridized with the aptamer was released as a trigger DNA due to specific recognition between the aptamer and target.Subsequently,ssDNA initiates the Exo Ⅲ-aided recycling to amplify the fluorescence signal,which was caused by N-methylmesoporphyrin IX(NMM)insertion into the G-quadruplex structure.This proposed strategy combines the excellent specificity between the aptamer and target,high sensitivity of the fluorescence signal by G-quadruplex and Exo Ⅲ-aided recycling amplification.We selected(50-1200 nmol/L) MUC1,a common tumor biomarker,as the proof-of-concept target to test the specificity of our aptasenso r.Results reveal that the sensor sensitively and selectively detected the target protein with limits of detection(LODs) of 3.68 and 12.83 nmol/L in buffer solution and 10% serum system,respectively.The strategy can be easily applied to other targets by simply substituting corresponding aptamers and has great potential in the diagnosis and monitoring of several diseases.
引用
收藏
页码:155 / 158
页数:4
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