A Target-Triggered DNAzyme Motor Enabling Homogeneous, Amplified Detection of Proteins

被引:124
作者
Chen, Junbo [1 ,2 ]
Zuehlke, Albert [2 ]
Deng, Bin [2 ]
Peng, Hanyong [2 ]
Hou, Xiandeng [1 ,3 ]
Zhang, Hongquan [2 ]
机构
[1] Sichuan Univ, Analyt & Testing Ctr, 29 Wangjiang Rd, Chengdu 610064, Sichuan, Peoples R China
[2] Univ Alberta, Fac Med & Dent, Dept Lab Med & Pathol, Div Analyt & Environm Toxicol, Edmonton, AB T6G 2G3, Canada
[3] Sichuan Univ, Coll Chem, 29 Wangjiang Rd, Chengdu 610064, Sichuan, Peoples R China
基金
加拿大自然科学与工程研究理事会;
关键词
DNA WALKER; GOLD NANOPARTICLES; MOLECULAR MOTOR; LIVING CELLS; ENZYME; NANOMACHINES; MECHANISM; HYBRIDIZATION; DEGRADATION; TRANSPORT;
D O I
10.1021/acs.analchem.7b03529
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We report here the concept of a self-powered, target-triggered DNA motor constructed by engineering a DNAzyme to adapt into binding-induced DNA assembly. An affinity ligand was attached to the DNAzyme motor via a DNA spacer, and a second affinity ligand was conjugated to the gold nanoparticle (AuNP) that was also decorated with hundreds of substrate strands serving as a high-density, three-dimensional track for the DNAzyme motor. Binding of a target molecule to the two ligands induced hybridization between the DNAzyme and its substrate on the AuNP, which are otherwise unable to spontaneously hybridize. The hybridization of DNAzyme with the substrate initiates the cleavage of the substrate and the autonomous movement of the DNAzyme along the AuNP. Each moving step restores the fluorescence of a dye molecule, enabling monitoring of the operation of the DNAzyme motor in real time. A simple addition or depletion of the cofactor Mg2+ allows for fine control of the DNAzyme motor. The motor can translate a single binding event into cleavage of hundreds of substrates, enabling amplified detection of proteins at room temperature without the need for separation.
引用
收藏
页码:12888 / 12895
页数:8
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