基于Vroman效应的表面等离子体共振生物传感器:面向癌症生物标志物检测

Seokheun Choi, J. Chae
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引用次数: 9

摘要

我们报道了一种利用Vroman效应在微流控装置中检测蛋白质的新技术。该传感器依赖于蛋白质在表面上吸附的竞争性质,直接取决于蛋白质的吸附强度。该传感器利用SPR(表面等离子体共振)进行高灵敏度的生物分子相互作用检测,利用Vroman效应进行高选择性检测。靶蛋白取代预吸附的弱亲和蛋白;然而,预吸附的强亲和力蛋白不会被靶蛋白取代。在一个微流体装置中,我们设计了两个金表面,上面覆盖着两种已知的蛋白质。该传感器允许选择性蛋白质检测,通过被目标蛋白质仅在一个表面上取代。SPR传感器图显示,白蛋白(Alb)、免疫球蛋白G (IgG)、纤维蛋白原(Fib)和甲状腺球蛋白(Tg) 4种不同的人血清蛋白对表面具有不同的吸附强度,个体间的竞争吸附控制着交换序列。基于交换反应,我们证明了该传感器对甲状腺癌生物标志物Tg具有高选择性。通过使用这项技术,我们绕过了必须依赖生物受体及其与传感器的连接,这是一个已知复杂且耗时的过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Surface plasmon resonance biosensor based on Vroman effect : Towards cancer biomarker detection
We report a new sensing technique of proteins using the Vroman effect in a microfluidic device. The sensor relies on the competitive nature of protein adsorption onto a surface, directly depending upon protein's adsorption strength. The sensor uses SPR (surface plasmon resonance) for highly sensitive biomolecular interactions detection and the Vroman effect for highly selective detection. A target protein displaces a pre-adsorbed weak-affinity protein; however a pre-adsorbed strong-affinity protein is not displaced by the target protein. In a microfluidic device, we engineer two gold surfaces covered by two known proteins. The sensor allows selective protein detection by being displaced by a target protein on only one of the surfaces. The SPR sensorgrams show that four different human serum proteins, albumin (Alb), immunoglobulin G (IgG), fibrinogen (Fib), and thyroglobulin (Tg) have different adsorption strengths to the surface and the competitive adsorption of individuals controls the exchange sequence. Based on the exchange reaction, we demonstrate that the sensor has a high selectivity for Tg which is a thyroid cancer biomarker. By using the technique, we bypass having to rely on bio-receptors and their attachment to transducers, a process known to be complex and time-consuming.
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