Kruse Marlen, Laux Eva-Maria, Bier Frank F, Hölzel Ralph
Fraunhofer Institute for Cell Therapy and Immunology, Branch Bioanalytics and Bioprocesses (IZI-BB), Potsdam-Golm, Germany.
University of Potsdam, Institute of Biochemistry and Biology, Potsdam-Golm, Germany.
Methods Mol Biol. 2025;2901:191-202. doi: 10.1007/978-1-0716-4394-5_15.
Many viruses bind multivalently to their target. The understanding of these binding processes can be beneficial for the development of effective treatments. Here we describe a protocol for measuring the oligovalent binding interaction of an influenza A virus X31 and a DNA nanostructure presenting one or several specifically designed binding peptides. The DNA nanostructure with its coupled binding peptides is complementary to the binding sites of the target protein hemagglutinin on the viral membrane. A detailed description of the sample preparation and the use of a DRX device to measure the interaction is given. The device allows for real-time measurement of the binding interaction without the necessity of labeling the virus or the peptide.
许多病毒会以多价方式与其靶标结合。了解这些结合过程有助于开发有效的治疗方法。在此,我们描述了一种用于测量甲型流感病毒X31与呈现一种或几种经过特殊设计的结合肽的DNA纳米结构之间的多价结合相互作用的实验方案。带有偶联结合肽的DNA纳米结构与病毒膜上靶蛋白血凝素的结合位点互补。文中给出了样品制备以及使用DRX设备测量相互作用的详细说明。该设备能够实时测量结合相互作用,而无需对病毒或肽进行标记。