Zaoui Kossay, Duhamel Stephanie
Department of Biochemistry, McGill University, Montreal, Quebec, Canada.
Rosalind and Morris Goodman Cancer Centre, McGill University, Montreal, Quebec, Canada.
Bio Protoc. 2020 May 5;10(9):e3609. doi: 10.21769/BioProtoc.3609.
The Ras homologous protein (Rho) GTPase subfamily, including RhoA, RhoB, and RhoC are small molecules (~21 kDa) that act as molecular switches in a wide range of signaling pathways to orchestrate biological processes associated with both physiological and tumorigenic cellular states. The Rho GTPases are crucial regulators of actin cytoskeleton rearrangements and FA dynamics and are required for effective cell migration and invasion, as well as cell cycle progression and apoptosis. The Rho GTPases activity is regulated by conformational switching between GTP-bound (active) and GDP-bound (inactive) states. This GTP/GDP cycling is tightly controlled by the guanine nucleotide exchange factors (GEFs), which function as activators by catalyzing the exchange of GDP for GTP and by the GTPase-activating proteins (GAPs), which enable hydrolysis of GTP leading to the Rho GTPase inactivation. Here, we describe a detailed protocol to perform a RhoB G-LISA activation assay to detect the level of GTP-loaded RhoB . This is the first colorimetric assay designed to specifically measure RhoB activation. This method was developed by adapting the RhoA G-LISA Activation Assay Kit (Cytoskeleton, Inc.) and allow the precise measurement of RhoB activity in less than 3 hours. This rapid methodology can be broadly used to assess the level of GTP-loaded RhoB in any kind of cellular models, to appreciate either the role RhoB activation in physiological processes, diseases, oncogenic transformation or for drug discovery in high throughput screens.
Ras同源蛋白(Rho)GTP酶亚家族,包括RhoA、RhoB和RhoC,是小分子(约21 kDa),在广泛的信号通路中充当分子开关,以协调与生理和致瘤细胞状态相关的生物学过程。Rho GTP酶是肌动蛋白细胞骨架重排和粘着斑动态变化的关键调节因子,是有效细胞迁移、侵袭以及细胞周期进程和凋亡所必需的。Rho GTP酶的活性通过GTP结合(活性)和GDP结合(非活性)状态之间的构象转换来调节。这种GTP/GDP循环受到鸟嘌呤核苷酸交换因子(GEFs)的严格控制,GEFs通过催化GDP与GTP的交换起激活剂的作用,还受到GTP酶激活蛋白(GAPs)的控制,GAPs能够使GTP水解导致Rho GTP酶失活。在此,我们描述了一种详细的方案,用于进行RhoB G-LISA激活测定以检测GTP负载的RhoB的水平。这是首个专门设计用于测量RhoB激活的比色测定法。该方法是通过改编RhoA G-LISA激活测定试剂盒(细胞骨架公司)开发的,可在不到3小时内精确测量RhoB活性。这种快速方法可广泛用于评估任何类型细胞模型中GTP负载的RhoB的水平,以了解RhoB激活在生理过程、疾病、致癌转化中的作用,或用于高通量筛选中的药物发现。