Base-Excision-Repair-Induced Construction of a Single Quantum-Dot-Based Sensor for Sensitive Detection of DNA Glycosylase Activity

被引:65
作者
Wang, Li-juan [1 ]
Ma, Fei [1 ]
Tang, Bo [1 ]
Zhang, Chun-yang [1 ]
机构
[1] Shandong Normal Univ, Coll Chem Chem Engn & Mat Sci,Key Lab Mol & Nano, Minist Educ,Shandong Prov Key Lab Clean Prod Fine, Collaborat Innovat Ctr Functionalized Probes Chem, Jinan 250014, Peoples R China
关键词
RESONANCE ENERGY-TRANSFER; LUNG-CANCER; 8-OXOGUANINE-DNA GLYCOSYLASE; SIGNAL AMPLIFICATION; MULTIPLEX DETECTION; CHINESE POPULATION; MOLECULE DETECTION; IN-VITRO; ASSAY; DAMAGE;
D O I
10.1021/acs.analchem.6b00664
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
DNA glycosylase is an initiating enzyme of cellular base excision repair pathway which is responsible for the repair of various DNA lesions and the maintenance of genomic stability, and the dysregulation of DNA glycosylase activity is associated with a variety of human pathology. Accurate detection of DNA glycosylase activity is critical to both clinical diagnosis and therapeutics, but conventional methods for the DNA glycosylase assay are usually time-consuming with poor sensitivity. Here, we demonstrate the base-excision-repair-induced construction of a single quantum dot (QD)-based sensor for highly sensitive measurement of DNA glycosylase activity. We use human 8-oxoguanine-DNA glycosylase 1 (hOGG1), which is responsible for specifically repairing the damaged 8-hydroxyguanine (8-oxoG, one of the most abundant and widely studied DNA damage products), as a model DNA glycosylase. In the presence of biotin-labeled DNA substrate, the hOGG1 may catalyze the removal of 8-oxo G from 8-oxoG center dot C base pairs to generate an apurinic/apyrimidinic (AP) site. With the assistance of apurinic/apyrimidinic endonuclease (APE1), the cleavage of the AP site results in the generation of a single-nucleotide gap. Subsequently, DNA polymerase,5 incorporates a Cy5-labeled dGTP into the DNA substrate to fill the gap. With the addition of streptavidin-coated QDs, a QD-DNA-Cy5 nanostructure is formed via specific biotin streptavidin binding, inducing the occurrence of fluorescence resonance energy transfer (FRET) from the QD to Cy5. The resulting Cy5 signal can be simply monitored by total internal reflection fluorescence (TIRF) imaging. The proposed method enables highly sensitive measurement of hOGG1 activity with a detection limit of 1.8 x 10(-6) U/mu L. Moreover, it can be used to measure the enzyme kinetic parameters and detect the hOGG1 activity in crude cell extracts, offering a powerful tool for biomedical research and clinical diagnosis.
引用
收藏
页码:7523 / 7529
页数:7
相关论文
共 47 条
[21]   Oxidative DNA damage and 8-hydroxy-2-deoxyguanosine DNA glycosylase/apurinic lyase in human breast cancer [J].
Li, DH ;
Zhang, WQ ;
Zhu, JJ ;
Chang, P ;
Sahin, A ;
Singletary, E ;
Bondy, M ;
Mitra, S ;
Lau, SS ;
Shen, JJ ;
DiGiovanni, J .
MOLECULAR CARCINOGENESIS, 2001, 31 (04) :214-223
[22]   Quality control by DNA repair [J].
Lindahl, T ;
Wood, RD .
SCIENCE, 1999, 286 (5446) :1897-1905
[23]   Label-free colorimetric assay for base excision repair enzyme activity based on nicking enzyme assisted signal amplification [J].
Liu, Xiaojuan ;
Chen, Mingqin ;
Hou, Ting ;
Wang, Xiuzhong ;
Liu, Shufeng ;
Li, Feng .
BIOSENSORS & BIOELECTRONICS, 2014, 54 :598-602
[24]   Multiplex detection of histone-modifying enzymes by total internal reflection fluorescence-based single-molecule detection [J].
Ma, Fei ;
Liu, Meng ;
Wang, Zi-yue ;
Zhang, Chun-yang .
CHEMICAL COMMUNICATIONS, 2016, 52 (06) :1218-1221
[25]   hOGG1 Ser326Cys polymorphism is associated with risk of bladder cancer in a Chinese population: A case-control study [J].
Ma, Lan ;
Chu, Haiyan ;
Wang, Meilin ;
Shi, Danni ;
Zhong, Dongyan ;
Li, Pu ;
Tong, Na ;
Yin, Changjun ;
Zhang, Zhengdong .
CANCER SCIENCE, 2012, 103 (07) :1215-1220
[26]   Imaging with total internal reflection fluorescence microscopy for the cell biologist [J].
Mattheyses, Alexa L. ;
Simon, Sanford M. ;
Rappoport, Joshua Z. .
JOURNAL OF CELL SCIENCE, 2010, 123 (21) :3621-3628
[27]   Base excision repair of oxidative DNA damage and association with cancer and aging [J].
Maynard, Scott ;
Schurman, Shepherd H. ;
Harboe, Charlotte ;
de Souza-Pinto, Nadja C. ;
Bohr, Vilhelm A. .
CARCINOGENESIS, 2009, 30 (01) :2-10
[28]   How DNA lesions are turned into mutations within cells? [J].
Pagès, V ;
Fuchs, RPP .
ONCOGENE, 2002, 21 (58) :8957-8966
[29]   Lighting-up the dynamics of telomerization and DNA replication by CdSe-ZnS quantum dots [J].
Patolsky, F ;
Gill, R ;
Weizmann, Y ;
Mokari, T ;
Banin, U ;
Willner, I .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (46) :13918-13919
[30]   DNA repair activity for oxidative damage and risk of lung cancer [J].
Paz-Elizur, T ;
Krupsky, M ;
Blumenstein, S ;
Elinger, D ;
Schechtman, E ;
Livneh, Z .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2003, 95 (17) :1312-1319