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用于阻抗检测活化蛋白C的富含树枝状大分子的一次性适体传感器。

Dendrimer enriched single-use aptasensor for impedimetric detection of activated protein C.

作者信息

Erdem Arzum, Congur Gulsah

机构信息

Ege University, Faculty of Pharmacy, Analytical Chemistry Department, 35100 Bornova, Izmir, Turkey; Ege University, The Institute of Natural and Applied Sciences, Biotechnology Department, 35100 Bornova, Izmir, Turkey.

Ege University, Faculty of Pharmacy, Analytical Chemistry Department, 35100 Bornova, Izmir, Turkey; Ege University, The Institute of Natural and Applied Sciences, Biotechnology Department, 35100 Bornova, Izmir, Turkey.

出版信息

Colloids Surf B Biointerfaces. 2014 May 1;117:338-45. doi: 10.1016/j.colsurfb.2014.03.003. Epub 2014 Mar 12.

Abstract

A novel impedimetric aptasensor for detection of human activated protein C (APC) was introduced for the first time in the present study. An enhanced sensor response was obtained using poly(amidoamine) (PAMAM) dendrimer having 16 succinamic acid surface groups (generation 2, G2-PS), that was modified onto the surface of screen printed graphite electrode (G2-PS/SPE). An amino modified DNA aptamer was then immobilized onto the surface of G2-PS modified SPE. The selective interaction of APT with its cognate protein, APC was investigated using different electrochemical techniques; differential pulse voltammetry (DPV), cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The microscopic characterization was consecutively performed before/after each modification/interaction step using scanning electron microscopy (SEM) and atomic force microscopy (AFM). The selectivity of aptasensor was tested in the presence of numerous proteins; protein C, thrombin, bovine serum albumin, factor Va and chromogenic substrate in different buffer mediums. The APC detection in the artificial serum; fetal bovine serum (FBS) was also performed impedimetrically. This dendrimer modified aptasensor technology brings several advantages: being single-use, fast screening with low-cost per measurement and resulting in sensitive detection of APC with the detection limits of 0.74 μg/mL (0.46 pmol in 35 μL sample) in buffer medium, and 2.03 μg/mL (1.27 pmol in 35 μL sample) in serum.

摘要

本研究首次介绍了一种用于检测人活化蛋白C(APC)的新型阻抗适配体传感器。使用具有16个琥珀酰胺酸表面基团的聚(酰胺胺)(PAMAM)树枝状大分子(第2代,G2-PS)获得了增强的传感器响应,该树枝状大分子被修饰在丝网印刷石墨电极(G2-PS/SPE)表面。然后将氨基修饰的DNA适配体固定在G2-PS修饰的SPE表面。使用不同的电化学技术研究了APT与其同源蛋白APC的选择性相互作用;差分脉冲伏安法(DPV)、循环伏安法(CV)和电化学阻抗谱(EIS)。在每个修饰/相互作用步骤之前/之后,依次使用扫描电子显微镜(SEM)和原子力显微镜(AFM)进行微观表征。在存在多种蛋白质的情况下测试了适配体传感器的选择性;蛋白C、凝血酶、牛血清白蛋白、因子Va和不同缓冲介质中的显色底物。还通过阻抗法在人工血清中检测了APC;胎牛血清(FBS)。这种树枝状大分子修饰的适配体传感器技术具有几个优点:一次性使用、每次测量成本低的快速筛选,并且能够灵敏地检测APC,在缓冲介质中的检测限为0.74μg/mL(35μL样品中为0.46pmol),在血清中的检测限为2.03μg/mL(35μL样品中为1.27pmol)。

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