Spatio-temporal dynamics of GEF-GTPase networks

GEF-GTPase 网络的时空动态

• 批准号: 8744288
• 负责人: Klaus M. Hahn
• 金额: $ 110.2万
• 依托单位: UNIV OF NORTH CAROLINA CHAPEL HILL
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-09-30 至 2018-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8744288
• 关键词: Actins; Address; Adhesions; Apoptosis; Architecture; Back; Behavior; Biochemical; Biochemical Genetics; Biological Assay; Biosensor; Cadherins; Cell Adhesion Molecules; Cell Nucleus; Cell Polarity; Cell physiology; Cell surface; Cell-Cell Adhesion; Cell-Matrix Junction; Cells; Complex; Coupled; Cues; Cytokinesis; Cytoskeleton; DNA Damage; Data; Dependency; Disease; Eukaryotic Cell; Event; Family; Feedback; Genetic Transcription; Goals; Guanine Nucleotide Exchange Factors; Guanosine Triphosphate; Guanosine Triphosphate Phosphohydrolases; Health; Heterogeneity; Human Genome; Hydrolysis; Image; Imagery; In Situ; Individual; Integral Membrane Protein; Integrins; Intercellular Junctions; Kinetics; Knowledge; Life; Light; Lipids; Location; Measures; Mechanics; Mediating; Methods; Microfilaments; Modeling; Molecular; Molecular Conformation; Network-based; Nuclear; Nuclear Envelope; Nucleotides; Pathway interactions; Phagocytosis; Play; Procedures; Process; Property; Protein Family; Proteins; Recruitment Activity; Regulation; Relative (related person); Reporting; Resolution; Role; Signal Transduction; Signaling Molecule; Signaling Protein; Spatial Distribution; Specificity; Stimulus; Structure; System; Testing; Time; Work; base; cell behavior; cell motility; computerized tools; design; feeding; in vivo; innovative technologies; mathematical model; member; migration; network architecture; novel; novel strategies; polymerization; programs; receptor; research study; response; rho; rho GTP-Binding Proteins; tool

DESCRIPTION (provided by applicant): Rho family GTPases is ubiquitous molecular switches that control extraordinarily diverse cellular processes. They are activated by guanine nucleotide exchange factors (GEFs) that are roughly 5-fold more numerous than the GTPases themselves and integrate the many cellular inputs controlling GTPase function. GEFs and GTPases form complex networks that are constituted transiently and locally for specific purposes. Biochemical, genetic, molecular, and structural analyses have unraveled a great deal about these critically important pathways, but the most important functional property, their spatio-temporal regulation, can only be fully understood in the context of intact cells. This PPG brings together team members with diverse expertise to develop innovative technologies enabling the study of GEF/GTPase networks in vivo, computational tools to extract network architecture and signaling kinetics from imaging data, and in-depth knowledge of cell behaviors critically dependent on GEF/GTPase dynamics: (Project 1- Hahn) will deliver GEF biosensors based on designs addressing different GEF structural classes. In a collaborative effort with Sondek, expert in GEF structure, different biosensor designs will report GEF activation by specific upstream inputs, and activation of endogenous GEFs. (Project 2- Danuser) will develop the ability to simultaneously image and/or photomanipulate the activity of any pair of GEFs and GTPases, for high resolution studies of GEF/GTPase spatio-temporal coordination. New computational tools will combine data from different experiments to model large networks, and to extract network architecture and signaling kinetics from imaging data. These methods will be tested in studies of complex GEF-GTPase feedback interactions. (Project 3- Hall): This biologically focused project will extend our work to multicellular systems. We will focus on GEF activation in cell-cell junctions and cryptic lamellipodia, and identify GEFs regulating collective migration. (Project 4- Burridge) will address the role of GEF/GTPase netvvorks in mechanotransduction, exploring novel findings regarding the mechanical regulation of RhoA signaling at cell-matrix and cell-cell adhesions during initiation of protrusions, and in the nucleus.

描述（由申请人提供）：Rho家族GTP酶是普遍存在的分子开关，控制非常多样化的细胞过程。它们被鸟嘌呤核苷酸交换因子（GEF）激活，GEF的数量大约是GTP酶本身的5倍，并整合了许多控制GTP酶功能的细胞输入。全球环境基金和全球贸易点构成了复杂的网络，这些网络是为特定目的在当地临时建立的。生物化学、遗传学、分子和结构分析已经揭示了很多关于这些至关重要的途径，但最重要的功能特性，它们的时空调控，只能在完整细胞的背景下才能完全理解。该PPG汇集了具有不同专业知识的团队成员，以开发创新技术，从而能够在体内研究GEF/GTdR网络，从成像数据中提取网络结构和信号动力学的计算工具，以及对严重依赖GEF/GTdR动力学的细胞行为的深入了解：（项目1- Hahn）将提供基于解决不同GEF结构类的设计的GEF生物传感器。在与全球环境基金结构专家Sondek的合作中，不同的生物传感器设计将报告特定上游输入的全球环境基金激活和内源性全球环境基金的激活。（项目2- Danuser）将发展对任何一对全球环境基金和全球贸易点的活动同时成像和/或光操纵的能力，以便对全球环境基金/全球贸易点的时空协调进行高分辨率研究。新的计算工具将结合来自不同实验的联合收割机数据来模拟大型网络，并从成像数据中提取网络结构和信号动力学。这些方法将在研究复杂的GEF-GTTRIM反馈相互作用中进行测试。（项目3-大厅）：这个以生物学为重点的项目将把我们的工作扩展到多细胞系统。我们将专注于GEF激活细胞连接和隐蔽板状伪足，并确定GEF调节集体迁移。（项目4- Burridge）将解决GEF/GTmannetvorks在机械转导中的作用，探索关于突起起始期间细胞-基质和细胞-细胞粘附处以及细胞核中RhoA信号传导的机械调节的新发现。