Dual atom transfer radical polymerization for ultrasensitive electrochemical DNA detection

被引:12
作者
Zheng, Xiaoke [1 ]
Liu, Qianrui [2 ]
Li, Manman [1 ]
Feng, Weisheng [1 ]
Yang, Huaixia [1 ]
Kong, Jinming [2 ]
机构
[1] Henan Univ Chinese Med, Pharm Coll, Zhengzhou 450046, Peoples R China
[2] Nanjing Univ Sci & Technol, Sch Environm & Biol Engn, Nanjing 210094, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrochemistry; Biosensor; Dual surface-initiated polymerization; DNA; STAR POLYMERS; LABEL-FREE; ARGET ATRP; AMPLIFICATION; GROWTH; COPOLYMERS; EATRP;
D O I
10.1016/j.bioelechem.2020.107462
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Atom transfer radical polymerization as a form of controlled/living radical polymerization is particularly attractive. In this work, dual atom transfer radical polymerization (ATRP) is reported for ultrasensitive DNA detection. Firstly, a peptide nucleic acid (PNA) modified with a thiol group was self-assembled on an electrode surface to capture target DNA (TDNA). The initiator of the first ATRP (ATRP-1), alpha-bromoisobutyric acid (BIBA), was linked to forming PNA/DNA heteroduplexes via coordination of Zr4+. The polymer chain formed by the monomer of ATRP-1 (2-(2-bromoisobutyryloxy) ethyl methacrylate, BIEM) was also one of initiators of the second ATRP (eATRP-2). The other initiator of eATRP-2 was additional BIBA. ATRP-1 involves activator regeneration by electron transfer (ARGET) ATRP, regulated via excess reducing agent. eATRP-2 is electrochemically mediated ATRP which can control the polymerization via an appropriate applied potential. Compared with one ATRP, more monomers of eATRP-2 modified with ferrocene are attached to electrode surface. Under optimal conditions, this dual ATRP strategy provides a low limit of detection (25 aM, similar to 150 molecules) with satisfactory selectivity and stability. Importantly, this strategy presents a useful prospect for the field of biomolecule detection. (C) 2020 Elsevier B.V. All rights reserved.
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页数:8
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