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Dynamic sandwich-type electrochemical assay for protein quantification and protein-protein interaction

机译:蛋白质定量和蛋白质 - 蛋白质相互作用的动态夹心式电化学测定

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摘要

The study of protein-protein interactions (PPIs) plays an important role in the understanding of biological systems; however, the established methods for PPI analysis often involve cumbersome sample preparation, multiple detecting steps, and costly instruments. Here we report a versatile and sensitive electrochemical method based on PPI-induced distinctive migration behavior of DNA deoxyribozyme (DNAzyme) on an electrode surface. In this method, the cleavage activity of DNAzyme toward the substrate DNA modified on the electrode surface is inversely correlated with the hydrodynamic diameter of the macromolecule attached to it. By making full use of this principle in an inexpensive electrochemical format that is named the dynamic sandwich-type electrochemical assay (dSTEA), we can probe into the presence of large macromolecules in a single-step procedure. Moreover, we can not only detect subpicomolar protein interaction events but also analyze the assembly of kinase in the whole cell extract. This novel signaling mechanism proposed in this work may broaden the applicability of DNAzyme-based electrochemical assays and it may also have great potential for applications in other interfacial sensor developments.
机译:蛋白质 - 蛋白质相互作用(PPI)的研究在理解生物系统中起重要作用;然而,PPI分析的建立方法通常涉及麻烦的样品制备,多种检测步骤和昂贵的仪器。在这里,我们报告了基于PPI诱导的DNA脱氧酶(DNAzyme)在电极表面上的敏感电化学方法。在该方法中,DNAzyme朝向在电极表面上改性的底物DNA的切割活性与附着于其上的大分子的液动力直径与其相反。通过以廉价的电化学形式充分利用该原理,该原理被称为动态夹层型电化学测定(DSTEA),我们可以在单步过程中探测大型大分子的存在。此外,我们不仅可以检测亚皮质摩尔蛋白相互作用事件,还可以分析全细胞提取物中激酶的组装。本作作品中提出的这种新的信号机制可以扩大基于DNAzyme的电化学测定的适用性,并且在其他界面传感器发射中也可能具有很大的应用潜力。

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