Institute of Chemistry, University Estadual Paulista (UNESP, São Paulo State University), CP 355, CEP 14800-900 Araraquara, São Paulo, Brazil.
Institute of Chemistry, University Estadual Paulista (UNESP, São Paulo State University), CP 355, CEP 14800-900 Araraquara, São Paulo, Brazil.
Biosens Bioelectron. 2014 Jul 15;57:96-102. doi: 10.1016/j.bios.2014.01.044. Epub 2014 Jan 31.
The transducer faradaic signals of molecularly receptive interfaces associated with specific target binding can be sensitively monitored by electrochemical impedance and/or capacitance spectroscopies. A comparative evaluation of both impedimetric (associated with charge transfer resistance) and capacitive (associated with faradaic density of states) approaches was undertaken using C-reactive protein (CRP) antigen and antibody interaction as biomolecular binding model. Aiming at constructing redox free (impedimetric) and redox tethered receptive (capacitive) interfaces engineered by self-assembly monolayer, CRP sensitivity and limit of detections were comparatively assessed regarding biosensor capabilities. Binding affinity constant between CRP and anti-CRP interfacial receptor sites were additionally evaluated by the Langmuir adsorption model. Both the impedimetric and capacitive approaches reported similar values of experimental analytical parameters albeit the latter was found to have the advantage of requiring no solution redox reporter thus making it highly suitable for use in multiplexing affinity arrays.
通过电化学阻抗和/或电容光谱,可以灵敏地监测与特定靶标结合相关的分子接受界面的换能器法拉第信号。使用 C 反应蛋白 (CRP) 抗原和抗体相互作用作为生物分子结合模型,对两种阻抗(与电荷转移电阻相关)和电容(与法拉第态密度相关)方法进行了比较评估。为了构建由自组装单层工程化的无氧化还原(阻抗)和氧化还原键合接受(电容)界面,针对生物传感器的能力,比较评估了 CRP 的敏感性和检测限。通过朗缪尔吸附模型进一步评估了 CRP 与抗 CRP 界面受体结合的结合亲和力常数。尽管后者具有不需要溶液氧化还原报告者的优势,使其非常适合用于多重亲和阵列,但是两种阻抗和电容方法都报告了类似的实验分析参数值。