Regulation of Rho family GTPases by heterotrimeric G proteins

异源三聚体 G 蛋白对 Rho 家族 GTP 酶的调节

• 批准号: 8042269
• 负责人: TOHRU KOZASA
• 金额: $ 33.76万
• 依托单位: UNIVERSITY OF ILLINOIS AT CHICAGO
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-09-01 至 2014-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8042269
• 关键词: ADRBK1 gene; Actins; Antibodies; Antineoplastic Agents; Biological Assay; Biosensor; Blood Platelets; Cardiovascular system; Cell Adhesion; Cell Differentiation process; Cell Shape; Cell physiology; Cells; Cellular Assay; Complex; Coupling; Cytoplasmic Tail; DH Domain; DNA Sequence Rearrangement; Defect; Development; Disease; Drug Delivery Systems; Embryonic Development; Family; Functional disorder; Funding; Future; G Protein-Coupled Receptor Signaling; G-Protein Signaling Pathway; G-Protein-Coupled Receptors; GTP-Binding Proteins; Gene Expression; Gene Family; Genome; Goals; Guanine Nucleotide Exchange Factors; Guanosine Triphosphate Phosphohydrolases; Heart Hypertrophy; Hemostatic function; Heterotrimeric GTP-Binding Proteins; Hypertension; Immune System and Related Disorders; Immune response; Integrin beta3; Integrins; Investigation; Kinetics; Link; Malignant Neoplasms; Marketing; Mass Spectrum Analysis; Measures; Mediating; Methods; Modification; Molecular; Monitor; Monoclonal Antibodies; Neoplasm Metastasis; Neurites; PH Domain; Pathway interactions; Pharmaceutical Preparations; Phenotype; Phosphorylation; Phosphorylation Site; Physiological; Physiology; Play; Post-Translational Protein Processing; RGS Domain; Regulation; Roentgen Rays; Role; Signal Pathway; Signal Transduction; Solid; Structure; Surface Plasmon Resonance; System; Thermodynamics; X-Ray Crystallography; base; cancer cell; cell growth; cell motility; cell transformation; drug development; migration; novel; reconstitution; research study; response; rho; rho guanine nucleotide exchange factor p115; tumor progression

DESCRIPTION (provided by applicant): The G12 family of heterotrimeric G proteins, which consists of G12 and G13, has been shown to mediate signals from GPCRs to RhoA activation. The monomeric GTPase RhoA modulates cellular processes, such as actin cytoskeletal rearrangement and gene expression. RGS-RhoGEF, specific GEFs (guanine nucleotide exchange factor) for RhoA with amino terminal RGS domain, acts as a direct link between G12/13 and RhoA. Studies have demonstrated the importance of G12/13-RGS-RhoGEF signaling pathway in a variety physiological functions. The involvement of this signaling pathway in disease conditions, such as cardiac hypertrophy, immunological dysfunction, or cancer metastasis has also been demonstrated. The long term goal of this proposal is to understand the molecular mechanism and function of heterotrimeric G protein-mediated regulation of Rho family GTPases. Immediate goal of this proposal is to elucidate the molecular mechanism and function of G12/13-RhoGEF signaling pathway. During the current funding period, we have made following progresses: (1) We developed a novel purification method for G12 and G13 and determined their crystal structures as well as G13-p115RhoGEF RGS complex. (2) We successfully applied similar purification strategy for Gq and determined the crystal structure of Gq-GRK2-Gbetagamma complex. Also, we discovered a novel RhoGEF, p63RhoGEF as a direct effector for Gq. (3) Using surface plasmon resonance (SPR) we established a system to measure kinetics and thermodynamics of G13-LARG interaction. The thermodynamic parameters suggested a significant conformational change of LARG during interaction with G13. (4) We discovered that G13 directly interacts with the cytoplasmic domain of the beta3andbeta integrin, and this interaction is required in mediating the integrin outside-in signaling leading to platelet spreading. Based on these progresses, we will investigate the following aims in this proposal. (1) We will determine X-ray crystal structures of the complex of G12 or G13 with p115RhoGEF construct including RGS domain and DH/PH domains. We will also perform SPR analysis to understand the dynamics of G12/13-p115RhoGEF interaction. (2) We hypothesize that phosphorylation of RGS-RhoGEF plays crucial regulatory role in G12/13-mediated signaling. With the combination of specific moloclonal antibodies and mass spectrometry, we will determine the phosphorylation sites of endogenous RGS-RhoGEF and characterize the functional role of these phosphorylation modifications in G12/13- mediated signal transduction. (3) We hypothesize that the signal coordination of G12/13-pathway and integrin-pathway is critical for cell invasion and migration of cancer cells. We will analyze the mechanism of this signal network using X-ray crystallography, reconstitution assays, and biosensor to monitor RhoA activity, and migration and invasion of cancer cells. PUBLIC HEALTH RELEVANCE: G protein-mediated signaling is the most widely used molecular mechanism to control a variety of physiological functions of our body. G protein-coupled receptors (GPCR) consist of the largest gene family of our genome and the most common drug target family. About 50% of current drugs on the market target GPCRs or their signaling components. Thus, the investigation of G protein- mediated signaling pathway is not only essential to understand our physiology but also critically important to develop novel drugs in future. In this project, I will focus on the G12/13-mediated signaling pathway, a specific G protein signaling pathway that is known to be important for various important cellular processes including cancer progression, cell transformation, cell shape changes, or cell growth and differentiation. Experiments were proposed to elucidate the structure of the signaling components of this pathway and also the dynamic changes of interaction between these components. Recently, we also found a novel signaling network between G12/13-signaling pathway and cell adhesion signaling pathway. This is a novel finding to connect these two important signaling systems. The experiments from atomic structure analysis to cellular assay system are proposed to understand this signal network. The results from this project will make crucial contribution to understand advancement of cancer phenotypes and form a solid basis for future anti-cancer drug development.

描述（由申请人提供）：由G12和G13组成的异源三聚体G蛋白G12家族已被证明可以介导从gpcr到RhoA激活的信号。单体GTPase RhoA调节细胞过程，如肌动蛋白细胞骨架重排和基因表达。RGS- rhogef是RGS结构域氨基末端RhoA的特异性gef（鸟嘌呤核苷酸交换因子），是G12/13与RhoA之间的直接联系。研究表明G12/13-RGS-RhoGEF信号通路在多种生理功能中的重要性。该信号通路参与疾病状况，如心脏肥大、免疫功能障碍或癌症转移也已被证实。本研究的长期目标是了解异三聚体G蛋白介导的Rho家族gtpase调控的分子机制和功能。本课题的近期目标是阐明G12/13-RhoGEF信号通路的分子机制和功能。在本次资助期内，我们取得了以下进展：(1)我们开发了一种新的纯化G12和G13的方法，并确定了它们的晶体结构以及G13- p115rhogef RGS复合物。(2)我们成功地对Gq采用了类似的纯化策略，并确定了Gq- grk2 - gbetagamma配合物的晶体结构。此外，我们还发现了一种新的RhoGEF， p63RhoGEF作为Gq的直接效应因子。(3)利用表面等离子体共振（SPR）建立了G13-LARG相互作用动力学和热力学测量系统。热力学参数表明LARG在与G13相互作用过程中发生了明显的构象变化。(4)我们发现G13直接与β 3和β整合素的细胞质结构域相互作用，这种相互作用是介导整合素外向内信号传导导致血小板扩散所必需的。基于这些进展，我们将在本提案中探讨以下目标。(1)我们将测定G12或G13与p115RhoGEF复合物的x射线晶体结构，包括RGS结构域和DH/PH结构域。我们还将进行SPR分析，以了解G12/13-p115RhoGEF相互作用的动力学。(2)我们假设RGS-RhoGEF的磷酸化在g12 /13介导的信号传导中起着至关重要的调节作用。通过结合特异性单克隆抗体和质谱分析，我们将确定内源性RGS-RhoGEF的磷酸化位点，并表征这些磷酸化修饰在G12/13介导的信号转导中的功能作用。(3)我们假设g12 /13通路和整合素通路的信号协调对癌细胞的侵袭和迁移至关重要。我们将使用x射线晶体学、重构分析和生物传感器来监测RhoA活性、癌细胞的迁移和侵袭，分析该信号网络的机制。