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Real-Time, Label-Free Detection of Biomolecular Interactions in Sandwich Assays by the Oblique-Incidence Reflectivity Difference Technique

机译:斜入射反射率差异技术实时,无标记地检测夹心测定中的生物分子相互作用

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One of the most important goals in proteomics is to detect the real-time kinetics of diverse biomolecular interactions. Fluorescence, which requires extrinsic tags, is a commonly and widely used method because of its high convenience and sensitivity. However, in order to maintain the conformational and functional integrality of biomolecules, label-free detection methods are highly under demand. We have developed the oblique-incidence reflectivity difference (OI-RD) technique for label-free, kinetic measurements of protein-biomolecule interactions. Incorporating the total internal refection geometry into the OI-RD technique, we are able to detect as low as 0.1% of a protein monolayer, and this sensitivity is comparable with other label-free techniques such as surface plasmon resonance (SPR). The unique advantage of OI-RD over SPR is no need for dielectric layers. Moreover, using a photodiode array as the detector enables multi-channel detection and also eliminates the over-time signal drift. In this paper, we demonstrate the applicability and feasibility of the OI-RD technique by measuring the kinetics of protein-protein and protein-small molecule interactions in sandwich assays.
机译:蛋白质组学最重要的目标之一是检测各种生物分子相互作用的实时动力学。需要外部标签的荧光,由于其便利性和敏感性高,是一种普遍且广泛使用的方法。然而,为了维持生物分子的构象和功能完整性,无标记检测方法的需求量很大。我们已经开发了斜入射反射率差异(OI-RD)技术,用于无标记的蛋白质-生物分子相互作用的动力学测量。将总内部复染几何结构整合到OI-RD技术中,我们能够检测到低至0.1%的蛋白质单层,并且这种灵敏度可与其他无标记技术(例如表面等离振子共振(SPR))媲美。 OI-RD优于SPR的独特优势是不需要介电层。此外,使用光电二极管阵列作为检测器可以进行多通道检测,并且还消除了超时信号漂移。在本文中,我们通过在三明治试验中测量蛋白质-蛋白质和蛋白质-小分子相互作用的动力学来证明OI-RD技术的适用性和可行性。

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