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Analogies Between Digital Radio and Chemical Orthogonality as a Method for Enhanced Analysis of Molecular Recognition Events

机译:数字无线电和化学正交性之间的类比作为一种增强的分子识别事件分析方法

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摘要

Acoustic wave biosensors are a real-time, label-free biosensor technology, which have been exploited for the detection of proteins and cells. One of the conventional biosensor approaches involves the immobilization of a monolayer of antibodies onto the surface of the acoustic wave device for the detection of a specific analyte. The method described within includes at least two immobilizations of two different antibodies onto the surfaces of two separate acoustic wave devices for the detection of several analogous analytes. The chemical specificity of the molecular recognition event is achieved by virtue of the extremely high (nM to pM) binding affinity between the antibody and its antigen. In a standard ELISA (Enzyme-Linked ImmunoSorbent Assay) test, there are multiple steps and the end result is a measure of what is bound so tightly that it does not wash away easily. The fact that this “gold standard” is very much not real time, masks the dance that is the molecular recognition event. X-Ray Crystallographer, Ian Wilson, demonstrated more than a decade ago that antibodies undergo conformational change during a binding event[1, 2]. Further, it is known in the arena of immunochemistry that some antibodies exhibit significant cross-reactivity and this is widely termed antibody promiscuity. A third piece of the puzzle that we will exploit in our system of acoustic wave biosensors is the notion of chemical orthogonality. These three biochemical constructs, the dance, antibody promiscuity and chemical orthogonality will be combined in this paper with the notions of in-phase (I) and quadrature (Q) signals from digital radio to manifest an approach to molecular recognition that allows a level of discrimination and analysis unobtainable without the aggregate. As an example we present experimental data on the detection of TNT, RDX, C4, ammonium nitrate and musk oil from a system of antibody-coated acoustic wave sensors.
机译:声波生物传感器是一种实时,无标签的生物传感器技术,已被用于检测蛋白质和细胞。一种常规的生物传感器方法涉及将单层抗体固定在声波装置的表面上,以检测特定的分析物。所描述的方法包括将两种不同抗体至少两次固定在两个单独的声波装置的表面上,用于检测几种类似的分析物。分子识别事件的化学特异性是通过抗体与其抗原之间的极高结合亲和力实现的。在标准ELISA(酶联免疫吸附测定)测试中,有多个步骤,最终结果是非常紧密地结合在一起以至于无法轻易洗去的度量。这个“金标准”不是实时的事实,掩盖了作为分子识别事件的舞蹈。 X射线晶体学专家Ian Wilson证明,十多年前,抗体在结合过程中发生构象变化[1,2]。此外,在免疫化学领域中已知某些抗体表现出显着的交叉反应性,这被广泛称为抗体混杂。我们将在声波生物传感器系统中利用的第三个难题是化学正交性的概念。本文将结合舞蹈,抗体混杂和化学正交性这三个生化结构与数字无线电的同相(I)和正交(Q)信号的概念相结合,以体现一种分子识别方法,该方法可以使没有汇总,就无法获得歧视和分析。作为示例,我们介绍了从抗体包被的声波传感器系统中检测TNT,RDX,C4,硝酸铵和麝香油的实验数据。

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