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使用肼电催化剂制备用于生物分子检测的一次性传感器。

Fabrication of disposable sensors for biomolecule detection using hydrazine electrocatalyst.

作者信息

Shiddiky Muhammad J A, Rahman Md Aminur, Cheol Chang Seung, Shim Yoon-Bo

机构信息

Department of Chemistry and Center for Innovative BioPhysio Sensor Technology, Pusan National University, Busan 609-735, South Korea.

出版信息

Anal Biochem. 2008 Aug 15;379(2):170-5. doi: 10.1016/j.ab.2008.05.004. Epub 2008 May 7.

DOI:10.1016/j.ab.2008.05.004
PMID:18513487
Abstract

We have developed electrochemical DNA and protein sensors on screen-printed electrodes based on the catalytic activity of hydrazine. The sensors use carboxylic acid-functionalized conductive polymer, poly-5,2',5',2''-terthiophene-3'-carboxylic acid (polyTTCA) to make firm immobilization of dendrimer (DEN) through the covalent bond formation between the carboxylic acid groups of polymer and amine groups of dendrimer. The gold nanoparticles (AuNPs) were adsorbed on the remaining amine groups of dendrimer. The thiolated DNA probe or primary antibody was subsequently immobilized on the AuNP-covered dendrimer surfaces. Avidin-labeled hydrazine (Av-Hyd) was then immobilized on the sensor surfaces through the avidin-biotin interaction between the Av-Hyd unit and the biotinylated DNA or secondary antibody. The electrocatalytic reduction current of H(2)O(2) was measured by differential pulse voltammetry. The detection signal was amplified by the polyTTCA/DEN assembly loaded with AuNPs (approximately 3.5 nm) onto which target analyte-linked Av-Hyd was adsorbed. Linear dynamic ranges for the electrocatalytic detection of DNA and human immunoglobulin G (IgG) extending from 50 fM to 7.5 nM and from 40 fg/ml to 2.5 ng/ml, respectively, were observed along with detection limits of approximately 30 fM and 25 fg/ml, respectively. The low detection limit of the disposable sensors offers good promise for practical DNA and protein detection.

摘要

我们基于肼的催化活性,在丝网印刷电极上开发了电化学DNA和蛋白质传感器。这些传感器使用羧酸功能化的导电聚合物聚-5,2',5',2''-三联噻吩-3'-羧酸(聚TTCA),通过聚合物的羧酸基团与树枝状大分子的胺基团之间形成共价键,实现树枝状大分子(DEN)的牢固固定。金纳米颗粒(AuNPs)吸附在树枝状大分子剩余的胺基团上。随后,将硫醇化的DNA探针或一抗固定在覆盖有AuNP的树枝状大分子表面。然后,通过Av-Hyd单元与生物素化DNA或二抗之间的抗生物素蛋白-生物素相互作用,将抗生物素蛋白标记的肼(Av-Hyd)固定在传感器表面。通过差分脉冲伏安法测量H₂O₂的电催化还原电流。检测信号通过负载有AuNPs(约3.5 nm)的聚TTCA/DEN组装体进行放大,目标分析物连接的Av-Hyd吸附在该组装体上。观察到DNA和人免疫球蛋白G(IgG)电催化检测的线性动态范围分别从50 fM延伸至7.5 nM和从40 fg/ml延伸至2.5 ng/ml,检测限分别约为30 fM和25 fg/ml。这种一次性传感器的低检测限为实际的DNA和蛋白质检测提供了良好的前景。

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