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Diazonium-Protein Adducts for Graphite Electrode Microarrays Modification: Direct and Addressed Electrochemical Immobilization

机译:用于石墨电极微阵列修饰的重氮蛋白质加合物:直接和寻址的电化学固定

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摘要

Diazonium cation electrodeposition was investigated for the direct and electro-addressed immobilization of proteins.For the first time,this reaction was triggered directly onto diazonium-modified proteins.Screen-printed (SP) graphite electrode microarrays were studied as active support for this immobilization.A 10-microelectrode (eight working electrodes,0.2 mm~2 each; one reference; and one auxiliary) setup was used to study the addressing possibilities of the method.These electrode microarrays were shown to be able to covalently graft diazonium cations through electrochemical reduction.Cyclic voltammetry and X-ray photoelectron spectroscopy were used to characterize the electrochemical grafting onto our SP graphite surface and suggested that a diazonium monolayer was deposited.Rabbit and human immunoglobulins (IgGs) were then chemically coupled to an aniline derivative (4-carboxymethylaniline),followed by diazotation to form an aryl diazonium function available for the electrodeposition.These modified proteins were both successfully electro-addressed at the surface of the graphite electrodes without crosstalk or interference.The immuno-biochip obtained using this novel approach enabled the specific detection of anti-rabbit IgG antibodies with a detection limit of 50 fmol of protein.A promising strategy to immobilize markedly different biological entities was then presented,providing an excellent spatial specificity of the electro-addressing.
机译:研究了重氮阳离子电沉积对蛋白质的直接和电寻址固定化作用。首次将这种反应直接触发到重氮修饰的蛋白质上。研究了丝网印刷(SP)石墨电极微阵列作为该固定化的活性支持物。使用10个微电极(八个工作电极,每个0.2 mm〜2;一个参比电极和一个辅助电极)设置来研究该方法的寻址可能性。这些电极微阵列显示出能够通过电化学还原共价接枝重氮阳离子的方法。用循环伏安法和X射线光电子能谱表征SP石墨表面上的电化学接枝现象,表明沉积了重氮单层,然后将兔和人免疫球蛋白(IgG)化学偶联至苯胺衍生物(4-羧甲基苯胺)然后重氮化形成芳基重氮官能团,可用于电沉积这些修饰的蛋白都成功地在石墨电极表面进行了电寻址,而没有串扰或干扰。使用这种新方法获得的免疫生物芯片能够特异性检测抗兔IgG抗体,其检测极限为50 fmol。然后提出了一种有前途的策略来固定明显不同的生物实体,从而提供了电寻址的出色空间特异性。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2005年第51期|p.18328-18332|共5页
  • 作者单位

    Contribution from the Laboratoire de Genie Enzymatique et Biomoleculaire,UMR 5013 EMB2,CNRS Universite Claude Bernard Lyon 1,Bat CPE,43,boulevard du 11 Novembre 1918,69622 Villeurbanne,Cedex,France;

    Contribution from the Laboratoire de Genie Enzymatique et Biomoleculaire,UMR 5013 EMB2,CNRS Universite Claude Bernard Lyon 1,Bat CPE,43,boulevard du 11 Novembre 1918,69622 Villeurbanne,Cedex,France;

    Contribution from the Laboratoire de Genie Enzymatique et Biomoleculaire,UMR 5013 EMB2,CNRS Universite Claude Bernard Lyon 1,Bat CPE,43,boulevard du 11 Novembre 1918,69622 Villeurbanne,Cedex,France;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

  • 入库时间 2022-08-18 03:24:23

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