A surface-initiated enzymatic polymerization strategy for electrochemical DNA sensors

被引:47
作者
Wan, Ying [1 ]
Xu, Hui [2 ]
Su, Yan [1 ]
Zhu, Xinhua [1 ]
Song, Shiping [3 ]
Fan, Chunhai [3 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Mech Engn, Nanjing 210094, Jiangsu, Peoples R China
[2] Ludong Univ, Sch Chem & Mat Sci, Yantai 264025, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Appl Phys, Phys Biol Lab, Shanghai 201800, Peoples R China
基金
美国国家科学基金会;
关键词
Electrochemical DNA (E-DNA) sensor; Surface initiated enzymatic polymerization (SIEP); Terminal deoxynucleotidyl transferase (TdT); TdT-mediated extension reaction; ROLLING CIRCLE AMPLIFICATION; SEQUENCE-SPECIFIC DETECTION; STRAND-DISPLACEMENT AMPLIFICATION; MEDIATED ISOTHERMAL AMPLIFICATION; FEMTOMOLAR DNA; CHRONOCOULOMETRIC DNA; HYBRIDIZATION; BIOSENSORS; TRANSDUCTION; GENERATION;
D O I
10.1016/j.bios.2012.09.017
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this work, we report a novel strategy of electrochemical DNA (E-DNA) sensor based on surface initiated enzymatic polymerization (SIEP). This DNA sensor employs a capture DNA probe labeled with thiol at its 3' terminal to be immobilized at gold electrode via gold-thiol chemistry. Oligo (ethylene glycol) -terminated thiols (SH-OEGs) are then used to prepare an oligonucleotide-incorporated nonfouling surface (ONS). After the sequence-specific recognition of target DNA, terminal deoxynucleotidyl transferase (TdT) is employed to catalyze the sequential addition of deoxynucleotides (dNTPs) at the 3'-OH group of target DNA without template. During the TdT-mediated extension reaction, by using biotinlated 2'-deoxyadenosine 5'-triphosphate (biotin-dATP), biotin labels are incorporated into the SIEP-generated long single-stranded DNA (ssDNA). Specific binding of avidin-horseradish peroxidase (Av-HRP) to the biotin label leads to enzyme turnover-based signal transduction. By using this new strategy, we demonstrated the high picomolar sensitivity and a broad detection range of six orders of magnitude. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:526 / 531
页数:6
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