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Real Time Measurements of Membrane Protein:Receptor Interactions Using Surface Plasmon Resonance (SPR)

机译:膜蛋白的实时测量:使用表面等离子体共振(SPR)的受体相互作用

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摘要

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).
机译:蛋白质-蛋白质相互作用对于大多数(如果不是全部)生理过程至关重要,而了解这种相互作用的性质是生物学研究的中心步骤。表面等离子体共振(SPR)是一种灵敏的检测技术,可实时进行无标记的生物分子相互作用研究。在典型的SPR实验中,一种成分(通常是蛋白质,称为“配体”)被固定在传感器芯片表面上,而另一种成分(“分析物”)在溶液中游离并注入到表面上。测量分析物与配体的缔合和解离,并实时绘制在称为感觉图的图表上,从中得出平衡前和平衡数据。由于无标签,消耗少量材料并提供平衡前动力学数据,因此在研究蛋白质相互作用动力学时,SPR通常成为首选方法。但是,必须记住,由于该方法的高灵敏度,因此需要仔细分析获得的数据,并需要其他生化方法的支持。 SPR由于消耗少量的纯化物质,并且与脂质和去污剂相容,因此特别适用于研究膜蛋白。该协议描述了表征膜蛋白(ABC转运蛋白)和可溶性蛋白(转运蛋白的同源底物结合蛋白)相互作用的动力学特性的SPR实验。

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