Pierceall William E, Zhang Lixin, Hughes Dallas E
Cetek Corporation, Marlborough, MA, USA.
Methods Mol Biol. 2004;261:187-98. doi: 10.1385/1-59259-762-9:187.
Protein-protein interactions are instrumental in virtually all biological processes and their understanding will shed light on designing novel and effective drugs for therapeutic interventions targeting the pathways in which they function. Protein-protein interactions have been studied using many genetic and biochemical methods, most recently, affinity capillary electrophoresis (ACE). We used ACE as a high-throughput screening assay to establish and define binding interactions between a therapeutic target protein and chemical entities from natural product or synthetic chemical libraries. Furthermore, ACE has demonstrated its value in the measurement of binding constants, the estimation of kinetic rate constants, and the determination of the stoichiometry of protein-protein interactions. Herein, we will describe qualitatively several assay formats using ACE for detecting protein-protein interactions, and discuss their advantages and limitations.
蛋白质-蛋白质相互作用几乎在所有生物过程中都起着重要作用,对它们的理解将有助于设计针对其发挥作用的途径的新型有效治疗药物。人们已经使用了许多遗传和生化方法来研究蛋白质-蛋白质相互作用,最近又采用了亲和毛细管电泳(ACE)。我们将ACE用作高通量筛选分析方法,以建立并确定治疗靶点蛋白与天然产物或合成化学文库中的化学实体之间的结合相互作用。此外,ACE已在结合常数的测量、动力学速率常数的估算以及蛋白质-蛋白质相互作用化学计量的测定中展现出其价值。在此,我们将定性描述几种使用ACE检测蛋白质-蛋白质相互作用的分析形式,并讨论它们的优缺点。