Sun Wei, Vanhooke Janeen L, Sondek John, Zhang Qisheng
Division of Medicinal Chemistry & Natural Products, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
J Biomol Screen. 2011 Aug;16(7):717-23. doi: 10.1177/1087057111408420. Epub 2011 May 18.
GTPase-activating proteins of ADP-ribosylation factors (ARFGAPs) play key cellular roles in vesicle production and trafficking, adhesion, migration, and development. Dysfunctional regulation of ARFGAPs has been implicated in various diseases, including cancer, Alzheimer disease, and autism. Unfortunately, there are few mechanistic details describing how ARFGAPs contribute to disease states. In this regard, it would be extremely helpful to have a set of small molecules that selectively and directly modulate specific ARFGAPs as probes to dissect ARFGAP-regulated cell signaling under various conditions. Currently, such probes are lacking, and their identification is hampered by the lack of a suitable high-throughput assay to monitor ARFGAP activity. Here, the authors describe and validate a robust high-throughput assay using fluorescence polarization to monitor the ability of diverse ARFGAPs to enhance the capacity of ARF1 to hydrolyze guanosine triphosphate.
ADP核糖基化因子(ARF)的GTP酶激活蛋白(ARFGAP)在囊泡产生与运输、黏附、迁移及发育过程中发挥着关键的细胞作用。ARFGAP的功能失调与包括癌症、阿尔茨海默病和自闭症在内的多种疾病有关。遗憾的是,关于ARFGAP如何导致疾病状态的机制细节很少。在这方面,拥有一组能够选择性且直接调节特定ARFGAP的小分子作为探针,以剖析各种条件下ARFGAP调节的细胞信号传导,将非常有帮助。目前,此类探针尚不存在,而且由于缺乏合适的高通量检测方法来监测ARFGAP活性,其鉴定工作受到阻碍。在此,作者描述并验证了一种强大的高通量检测方法,该方法利用荧光偏振来监测多种ARFGAP增强ARF1水解三磷酸鸟苷能力的情况。