Livnat Levanon Nurit, Vigonsky Elena, Lewinson Oded
Department of Biochemistry, The Bruce and Ruth Rappaport Faculty of Medicine, The Technion-Israel Institute of Technology.
Department of Biochemistry, The Bruce and Ruth Rappaport Faculty of Medicine, The Technion-Israel Institute of Technology;
J Vis Exp. 2014 Nov 29(93):e51937. doi: 10.3791/51937.
Protein-protein interactions are pivotal to most, if not all, physiological processes, and understanding the nature of such interactions is a central step in biological research. Surface Plasmon Resonance (SPR) is a sensitive detection technique for label-free study of bio-molecular interactions in real time. In a typical SPR experiment, one component (usually a protein, termed 'ligand') is immobilized onto a sensor chip surface, while the other (the 'analyte') is free in solution and is injected over the surface. Association and dissociation of the analyte from the ligand are measured and plotted in real time on a graph called a sensogram, from which pre-equilibrium and equilibrium data is derived. Being label-free, consuming low amounts of material, and providing pre-equilibrium kinetic data, often makes SPR the method of choice when studying dynamics of protein interactions. However, one has to keep in mind that due to the method's high sensitivity, the data obtained needs to be carefully analyzed, and supported by other biochemical methods. SPR is particularly suitable for studying membrane proteins since it consumes small amounts of purified material, and is compatible with lipids and detergents. This protocol describes an SPR experiment characterizing the kinetic properties of the interaction between a membrane protein (an ABC transporter) and a soluble protein (the transporter's cognate substrate binding protein).
蛋白质-蛋白质相互作用对于大多数(即便不是所有)生理过程都至关重要,而了解此类相互作用的本质是生物学研究的核心步骤。表面等离子体共振(SPR)是一种用于实时无标记研究生物分子相互作用的灵敏检测技术。在典型的SPR实验中,一种成分(通常是一种蛋白质,称为“配体”)固定在传感器芯片表面,而另一种成分(“分析物”)在溶液中是游离的,并注入到表面上方。分析物与配体的结合和解离会被实时测量并绘制在一张称为传感图的图表上,由此可得出平衡前和平衡数据。由于无标记、消耗材料量低且能提供平衡前动力学数据,SPR常常成为研究蛋白质相互作用动力学时的首选方法。然而,必须牢记,由于该方法灵敏度高,所获得的数据需要仔细分析,并由其他生化方法加以佐证。SPR特别适合研究膜蛋白,因为它消耗少量纯化材料,并且与脂质和去污剂兼容。本方案描述了一个SPR实验,该实验表征了一种膜蛋白(一种ABC转运蛋白)与一种可溶性蛋白(该转运蛋白的同源底物结合蛋白)之间相互作用的动力学特性。