A fabrication strategy for protein sensors based on an electroactive molecularly imprinted polymer: Cases of bovine serum albumin and trypsin sensing

被引:16
作者
Zhao, Wei [1 ]
Li, Bing [1 ]
Xu, Sheng [1 ]
Zhu, Ye [2 ]
Liu, Xiaoya [1 ]
机构
[1] Jiangnan Univ, Sch Chem & Mat Engn, Key Lab Synthet & Biol Colloids, Minist Educ, Wuxi 214122, Jiangsu, Peoples R China
[2] Jiangnan Univ, Int Joint Res Ctr Photorespons Mol & Mat, 1800 Lihu Ave, Wuxi 214122, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Molecularly imprinted polymer; Self-assembly; Protein recognition; Electrochemistry; DRUG-DELIVERY; SOLID-PHASE; NANOPARTICLES; RECOGNITION; BIOSENSOR; LIQUID; COMPOSITES; PROTAMINE; ELECTRODE; ANTIBODY;
D O I
10.1016/j.aca.2020.04.023
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A high-performance molecularly imprinted sensing platform inspired by natural recognition mechanisms was fabricated to detect protein by employing a linear electro-polymerizable molecularly imprinted polymer as macromonomer. This was achieved via the combination of a biosensor fabrication with a self-assembly imprinting technique without the use of chemical labels. An amphipathic electroactive copolymer was designed as macro-monomer to maintain structural integrity of the protein template via self-assembly, resulting in generation of a 3D construction around the protein molecule to form imprinted sites. Electro-polymerization was utilized not only to anchor imprinted sites but also to enhance electron transfer. The adaptable sensing platform was based on a strengthened recognition reaction between the MIP layer and template protein after the generation of an electroactive network. Bovine serum albumin (BSA) and trypsin were used as model proteins to investigate the method's generality, which gave broad detection ranges of 10(-14)-10(-5) mg mL(-1) for BSA and 10(-13)-10(-8) mg mL(-1) for trypsin. These results indicate that the proposed fabrication offers an effective and versatile strategy for protein recognition. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:25 / 34
页数:10
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