Kaserer Alla O, Andi Babak, Cook Paul F, West Ann H
Department of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma, USA.
Methods Enzymol. 2010;471:59-75. doi: 10.1016/S0076-6879(10)71004-1. Epub 2010 Mar 1.
For both prokaryotic and eukaryotic His-Asp phosphorelay signaling pathways, the rates of protein phosphorylation and dephosphorylation determine the stimulus-to-response time frame. Thus, kinetic studies of phosphoryl group transfer between signaling partners are important for gaining a full understanding of how the system is regulated. In many cases, the phosphotransfer reactions are too fast for rates to be determined by manual experimentation. Rapid quench flow techniques thus provide a powerful method for studying rapid reactions that occur in the millisecond time frame. In this chapter, we describe experimental design and procedures for kinetic characterization of the yeast SLN1-YPD1-SSK1 osmoregulatory phosphorelay system using a rapid quench flow kinetic instrument.
对于原核生物和真核生物的组氨酸-天冬氨酸磷酰基转移信号通路而言,蛋白质磷酸化和去磷酸化的速率决定了刺激到反应的时间框架。因此,对信号传导伙伴之间磷酰基转移进行动力学研究,对于全面理解该系统的调控方式至关重要。在许多情况下,磷酸转移反应太快,以至于无法通过人工实验来测定其速率。因此,快速淬灭流动技术为研究在毫秒时间框架内发生的快速反应提供了一种强大的方法。在本章中,我们描述了使用快速淬灭流动动力学仪器对酵母SLN1-YPD1-SSK1渗透调节磷酰基转移系统进行动力学表征的实验设计和程序。