Site-specific immobilization of a (His)6-tagged acetylcholinesterase on nickel nanoparticles for highly sensitive toxicity biosensors

被引:55
作者
Ganesana, Mallikarjunarao [1 ]
Istarnboulie, Georges [2 ]
Marty, Jean-Louis [2 ]
Noguer, Thierry [2 ]
Andreescu, Silvana [1 ]
机构
[1] Clarkson Univ, Dept Chem & Biomol Sci, Potsdam, NY 13699 USA
[2] Univ Perpignan, IMAGES EA4218, F-66860 Perpignan, France
基金
美国国家科学基金会;
关键词
His-tag affinity immobilization; Nickel nanoparticles; Acetylcholinesterase biosensor; Pesticides; HISTIDINE-TAGGED PROTEINS; SCREEN-PRINTED ELECTRODES; ORGANOPHOSPHORUS INSECTICIDES; GOLD NANOPARTICLES; CHOLINESTERASE; PESTICIDES; ENZYMES; SURFACE; FILMS;
D O I
10.1016/j.bios.2011.08.024
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
This paper reports site-specific affinity immobilization of(His)6-tagged acetylcholinesterase (AChE) onto Ni/NiO nanoparticles for the development of an electrochemical screen-printed biosensor for the detection of organophosphate pesticides. The method is based on the specific affinity binding of the His-tagged enzyme to oxidized nickel nanoparticle surfaces in the absence of metal chelators. This approach allows stable and oriented attachment of the enzyme onto the oxidized nickel through the external His residue in one-step procedure, allowing for fast and sensitive detection of paraoxon in the concentration range from 10(-8) to 10(-13) M. A detection limit of 10(-12) M for paraoxon was obtained after 20 min incubation. This method can be used as a generic approach for the immobilization of other His-tagged enzymes for the development of biosensors. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:43 / 48
页数:6
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