Baker R P, Urban S
Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Methods Enzymol. 2017;584:229-253. doi: 10.1016/bs.mie.2016.10.025. Epub 2016 Dec 7.
Intramembrane proteases are an ancient and diverse group of multispanning membrane proteins that cleave transmembrane substrates inside the membrane to effect a wide range of biological processes. As proteases, a clear understanding of their function requires kinetic dissection of their catalytic mechanism, but this is difficult to achieve for membrane proteins. Kinetic measurements in detergent systems are complicated by micelle fusion/exchange, which introduces an additional kinetic step and imposes system-specific behaviors (e.g., cooperativity). Conversely, kinetic analysis in proteoliposomes is hindered by premature substrate cleavage during coreconstitution, and lack of methods to quantify proteolysis in membranes in real time. In this chapter, we describe a method for the real-time kinetic analysis of intramembrane proteolysis in model liposomes. Our assay is inducible, because the enzyme is held inactive by low pH during reconstitution, and fluorogenic, since fluorescence emission from the substrate is quenched near lipids but restored upon proteolytic release from the membrane. The precise measurement of initial reaction velocities continuously in real time facilitates accurate steady-state kinetic analysis of intramembrane proteolysis and its inhibition inside the membrane environment. Using real data we describe a step-by-step strategy to implement this assay for essentially any intramembrane protease.
膜内蛋白酶是一类古老且多样的多跨膜蛋白,它们在膜内切割跨膜底物,以实现广泛的生物学过程。作为蛋白酶,要清楚了解其功能需要对其催化机制进行动力学剖析,但对于膜蛋白来说这很难实现。在去污剂系统中进行动力学测量会因胶束融合/交换而变得复杂,这会引入额外的动力学步骤并产生系统特异性行为(例如协同性)。相反,蛋白脂质体中的动力学分析受到重构过程中底物过早切割的阻碍,并且缺乏实时定量膜内蛋白水解的方法。在本章中,我们描述了一种用于在模型脂质体中对膜内蛋白水解进行实时动力学分析的方法。我们的测定是可诱导的,因为在重构过程中酶因低pH而保持无活性,并且是荧光性的,因为底物的荧光发射在脂质附近被淬灭,但在从膜上进行蛋白水解释放后恢复。实时连续精确测量初始反应速度有助于对膜内蛋白水解及其在膜环境中的抑制进行准确的稳态动力学分析。我们使用实际数据描述了一种逐步策略,用于对基本上任何膜内蛋白酶实施此测定。