Collapse of DNA Tetrahedron Nanostructure for "Off On" Fluorescence Detection of DNA Methyltransferase Activity

被引:58
作者
Zhou, Xiaoyan [1 ,2 ]
Zhao, Min [1 ]
Duan, Xiaolei [1 ]
Guo, Bin [1 ]
Cheng, Wei [3 ]
Ding, Shijia [1 ]
Ju, Huangxian [1 ,4 ]
机构
[1] Chongqing Med Univ, Coll Lab Med, Minist Educ, Key Lab Clin Lab Diagnost, Chongqing 400016, Peoples R China
[2] Qingdao Univ, Affiliated Hosp, Dept Clin Lab, Med Coll, Qingdao 266101, Peoples R China
[3] Chongqing Med Univ, Ctr Clin Mol Med Detect, Affiliated Hosp 1, Chongqing 400016, Peoples R China
[4] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210023, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
DNA nanotechnology; DNA tetrahedron; DNA methyltransferases; fluorescence biosensor; DNA methyltransferase inhibitors; HYBRIDIZATION CHAIN-REACTION; LIVING CELLS; IN-VIVO; CYTOSINE-5; METHYLTRANSFERASE; ELECTROCHEMICAL DETECTION; MOLECULAR BEACON; MESSENGER-RNA; ENZYME-FREE; METHYLATION; AMPLIFICATION;
D O I
10.1021/acsami.7b13551
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
As a potential detection technique, highly rigid and versatile functionality of DNA tetrahedron nanostructures is often used in biosensing systems. In this work, a novel multifunctional nanostructure has been developed as an "off-on" fluorescent probe for detection of target methyltransferase by integrating the elements of DNA tetrahedron, target recognition, and dual-labeled reporter. This sensing system is initially in an "OFF" state owing to the close proximity of fluorophores and quenchers. After the substrate is recognized by target methyltransferase, the DNA tetrahedron can be methylated to produce methylated DNA sites. These sites can be recognized and cut by the restriction endonuclease DpnI to bring about the collapse of the DNA tetrahedron, which leads to the separation of the dual-labeled reporters from the quenchers, and thus the recovery of fluorescence signal to produce an "ON" state. The proposed DNA tetrahedron-based sensing method can detect Dam methyltransferase in the range of 0.1-90 U mL(-1) with a detection limit of 0.045 U mL(-1) and shows good specificity and reproducibility for detection of Dam methyltransferase in a real sample. It has been successfully applied for screening various methylation inhibitors. Thus, this work possesses a promising prospect for detection of DNA methyltransfrase in the field of clinical diagnostics.
引用
收藏
页码:40087 / 40093
页数:7
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