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用于石墨电极微阵列修饰的重氮蛋白加合物:直接和定位电化学固定化

Diazonium-protein adducts for graphite electrode microarrays modification: direct and addressed electrochemical immobilization.

作者信息

Corgier Benjamin P, Marquette Christophe A, Blum Loïc J

机构信息

Laboratoire de Génie Enzymatique et Biomoléculaire, UMR 5013 EMB2, CNRS Université Claude Bernard Lyon 1, Bât CPE, 43, boulevard du 11 Novembre 1918, 69622 Villeurbanne, Cedex, France.

出版信息

J Am Chem Soc. 2005 Dec 28;127(51):18328-32. doi: 10.1021/ja056946w.

Abstract

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 mm2 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 cross-talk 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.

摘要

研究了重氮阳离子电沉积用于蛋白质的直接和电寻址固定化。首次将该反应直接引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这种固定化的活性载体。使用一个10微电极(八个工作电极,每个0.2平方毫米;一个参比电极;一个辅助电极)装置来研究该方法的寻址可能性。这些电极微阵列被证明能够通过电化学还原共价接枝重氮阳离子。循环伏安法和X射线光电子能谱用于表征在我们的SP石墨表面上的电化学接枝,并表明沉积了重氮单层。然后将兔和人免疫球蛋白(IgG)化学偶联到苯胺衍生物(4-羧甲基苯胺)上,接着进行重氮化以形成可用于电沉积的芳基重氮官能团。这些修饰的蛋白质都成功地在石墨电极表面进行了电寻址,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,检测限为50飞摩尔蛋白质。然后提出了一种固定显著不同生物实体很有前景的策略,提供了电寻址出色的空间特异性。

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