Mohan Kritika, Penner Reginald M, Weiss Gregory A
Department of Chemistry, University of California, Irvine, California.
Department of Chemical Engineering and Materials Science, University of California, Irvine, California.
Curr Protoc Chem Biol. 2015 Jun 1;7(2):53-72. doi: 10.1002/9780470559277.ch140213.
Virus electrodes address two major challenges associated with biosensing. First, the surface of the viruses can be readily tailored for specific, high affinity binding to targeted biomarkers. Second, the viruses are entrapped in a conducting polymer for electrical resistance-based, quantitative measurement of biomarker concentration. To further enhance device sensitivity, two different ligands can be attached to the virus surface, and increase the apparent affinity for the biomarker. In the example presented here, the two ligands bind to the analyte in a bidentate binding mode with a chelate-based avidity effect, and result in a 100 pM experimentally observed limit of detection for the cancer biomarker prostate-specific membrane antigen. The approach does not require enzymatic amplification, and allows reagent-free, real-time measurements. This article presents general protocols for the development of such biosensors with modified viruses for the enhanced detection of arbitrary target proteins.
病毒电极解决了与生物传感相关的两个主要挑战。首先,病毒表面可以很容易地进行定制,以实现与目标生物标志物的特异性、高亲和力结合。其次,病毒被包裹在导电聚合物中,用于基于电阻的生物标志物浓度定量测量。为了进一步提高设备灵敏度,可以将两种不同的配体连接到病毒表面,从而增加对生物标志物的表观亲和力。在本文给出的示例中,这两种配体以双齿结合模式与分析物结合,具有基于螯合的亲和力效应,实验观察到癌症生物标志物前列腺特异性膜抗原的检测限为100 pM。该方法不需要酶放大,并且允许进行无试剂实时测量。本文介绍了开发此类生物传感器的一般方案,该生物传感器使用经过修饰的病毒来增强对任意目标蛋白质的检测。