4.8 Article

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

期刊

BIOSENSORS & BIOELECTRONICS
卷 30, 期 1, 页码 43-48

出版社

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2011.08.024

关键词

His-tag affinity immobilization; Nickel nanoparticles; Acetylcholinesterase biosensor; Pesticides

资金

  1. National Science Foundation [0727861, 0954919]
  2. Direct For Mathematical & Physical Scien
  3. Division Of Materials Research [0954919] Funding Source: National Science Foundation
  4. Office Of The Director
  5. Office Of Internatl Science &Engineering [0727861] Funding Source: National Science Foundation

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据