{"title":"Biosensing with Virus Electrode Hybrids","authors":"Kritika Mohan, Reginald M. Penner, Gregory A. Weiss","doi":"10.1002/9780470559277.ch140213","DOIUrl":null,"url":null,"abstract":"<p>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. © 2015 by John Wiley & Sons, Inc.</p>","PeriodicalId":38051,"journal":{"name":"Current protocols in chemical biology","volume":"7 2","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2015-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current protocols in chemical biology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/9780470559277.ch140213","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 3
Abstract
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. © 2015 by John Wiley & Sons, Inc.
利用病毒电极杂交体进行生物传感
病毒电极解决了与生物传感相关的两个主要挑战。首先,病毒的表面可以很容易地与目标生物标志物进行特异性的、高亲和力的结合。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。为了进一步提高装置的灵敏度,可以将两种不同的配体附着在病毒表面,增加对生物标志物的表观亲和力。在本例中,这两种配体以双齿结合模式与分析物结合,具有基于螯合物的亲和力效应,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。该方法不需要酶扩增,并且允许无试剂,实时测量。本文介绍了这种生物传感器与修饰病毒的发展的一般方案,以增强检测任意靶蛋白。©2015 by John Wiley &儿子,Inc。
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