Cooperative SH2 and SH3 domain-mediated interactions at the adaptor protein Grb2

SH2 和 SH3 结构域介导的接头蛋白 Grb2 上的协同相互作用

• 批准号: 7883144
• 负责人: Jon C.D. Houtman
• 金额: $ 31.13万
• 依托单位: UNIVERSITY OF IOWA
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-05-01 至 2015-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7883144
• 关键词: Adaptor Signaling Protein; Address; Affinity; Arts; Asthma; Autoimmune Diseases; Binding; Biochemical; Biochemistry; Biological Models; Biophysics; Calorimetry; Cardiovascular Diseases; Complex; Computer Simulation; Consensus; Conserved Sequence; Data; Diabetes Mellitus; Disease; Exhibits; Future; Goals; Graft Rejection; Growth; Human; Hypersensitivity; Individual; Iowa; Knowledge; Lead; Ligand Binding; Ligands; Link; Malignant Neoplasms; Mediating; Methods; Modeling; Molecular; Multiprotein Complexes; Organ Transplantation; Physiological Processes; Production; Proline; Protein Biochemistry; Proteins; Public Health; Publishing; Regimen; Research; Role; Signal Pathway; Signal Transduction; Signaling Protein; Site; Specificity; System; T-Lymphocyte; TCR Activation; Techniques; Testing; Therapeutic; Therapeutic Agents; Titrations; Tyrosine; Universities; Work; analytical ultracentrifugation; base; cell type; clinically relevant; design; driving force; examination questions; human disease; in vivo; inhibitor/antagonist; innovation; insight; novel therapeutics; programs; protein activation; protein protein interaction; public health relevance; receptor; research study; sedimentation velocity; stoichiometry; therapy development

DESCRIPTION (provided by applicant): The ubiquitously expressed adaptor protein Grb2 is crucial for the activation and propagation of signaling pathways that control many human physiological processes. Along with its role in propagating signaling pathways downstream of activated receptors and adaptor proteins, the disregulated formation of Grb2-mediated complexes has been linked to numerous pathological conditions in humans, including cancer, diabetes, autoimmune disorders, allergies/asthma and cardiovascular disease. Grb2 is composed of a Src homology 2 (SH2) domain, which binds specific phosphorylated tyrosines, flanked by two Src homology 3 (SH3) domains, which associate with proline- rich sequences. The interaction of Grb2 with SH2 and SH3 domain ligands has been extensively examined. Because of this, Grb2 is the primary model system for our understanding of the activation and function of SH and SH3 domain-containing proteins. Although these studies have provided insight into potential ligands and the binding mechanism of Grb2 and other important signaling proteins, they have not clearly addressed several critical questions. An examination of these questions is important if we are to fully understand how Grb2 and other related proteins regulate the formation and function of clinically relevant complexes. Our long-term goal is to characterize how SH2 and SH3 domain- containing proteins control the formation and function of clinically relevant signaling complexes in order to facilitate the develop of therapeutic regimens for diseases linked to the disregulated formation of these complexes. The objective of this specific proposal is to comprehensively examine the Grb2- mediated complexes that form at an SH2 domain ligand, the adaptor protein LAT. Our central working hypothesis is that Grb2 forms cooperative interactions with both LAT and individual SH3 domain ligands that control the formation and function of these critical multiprotein signaling complexes. To test this hypothesis, we will 1) molecularly characterize the interaction of Grb2 with the SH3 domain ligands Sos1, HPK1 and c-Cbl, 2) determine the forces that drive the association of specific Grb2 SH3 domain ligands with LAT and 3) determine the role of SH3 domain ligands in the interaction of Grb2 with LAT. To achieve these aims, we will employ several innovative, state-of-the-art biophysical, and biochemical techniques, including our new, more robust analysis methods for isothermal titration calorimetry and sedimentation velocity analytical ultracentrifugation. The information gained from these studies will allow us to significantly advance our understanding of the binding mechanism of Grb2 and other related proteins to both SH2 and SH3 domains ligands. This will not only provide new insight into the formation of SH2 and SH3 domain-mediated signaling complexes, but will also facilitate the production and/or use of novel therapeutic agents for the treatment of debilitating human diseases. PUBLIC HEALTH RELEVANCE: This proposal will examine how cooperative protein-protein interactions control the specificity and binding capacity of the SH2 and SH3 domains of the ubiquitously expressed adaptor protein Grb2. The knowledge gained from this study will help to us to understand the activation and function of Grb2 and other related clinically important proteins, which is expected to provide critical information for the rational design and/or use of inhibitors for these proteins. These agents will be useful for the treatment of multiple human diseases, including cancer, cardiovascular disease, autoimmune diseases, asthma/ allergies and the rejection of transplanted organs.

描述（由申请人提供）：无处不在表达的衔接蛋白GRB2对于控制许多人类生理过程的信号传导途径的激活和传播至关重要。除了其在激活受体和衔接蛋白下游传播信号通路方面的作用外，GRB2介导的复合物的无调形成与人类的许多病理状况有关，包括癌症，糖尿病，自身免疫性疾病，过敏/哮喘和心血管疾病。 GRB2由SRC同源性2（SH2）结构域组成，该结构结合了特定的磷酸化酪氨酸，两侧是两个SRC同源性3（SH3）结构域，它们与脯氨酸序列相关联。 GRB2与SH2和SH3结构域配体的相互作用已被广泛研究。因此，GRB2是我们理解含Sh和SH3结构域蛋白的激活和功能的主要模型系统。尽管这些研究提供了对潜在配体以及GRB2和其他重要信号蛋白的结合机制的见解，但它们尚未清楚地解决了几个关键问题。如果我们要充分了解GRB2和其他相关蛋白如何调节临床相关复合物的形成和功能，那么对这些问题的检查很重要。我们的长期目标是表征含有蛋白质的SH2和SH3结构域如何控制临床相关信号复合物的形成和功能，以促进与与这些复合物无关形成相关的疾病的治疗方案的发展。该特定建议的目的是全面检查在SH2结构域配体（衔接蛋白LAT）下形成的GRB2介导的复合物。我们的中心工作假设是，GRB2与LAT和单个SH3结构域配体形成合作相互作用，这些配体控制着这些关键的多蛋白信号传导复合物的形成和功能。为了检验这一假设，我们将1）分子表征GRB2与SH3域配体SOS1，HPK1和C-CBL的相互作用，2）确定驱动特定Grb2 Sh3域配体与LAT和LAT 3的相关性的力，并确定SH3域在GRB2与LAT的相互作用中的作用。为了实现这些目标，我们将采用几种创新的，最先进的生物物理和生化技术，包括我们用于等温滴定热量法和沉降速度分析性超速离心的新型，更健壮的分析方法。从这些研究中获得的信息将使我们能够显着提高我们对GRB2和其他相关蛋白与SH2和SH3域配体的结合机制的理解。这不仅将为SH2和SH3域介导的信号传导复合物的形成提供新的见解，而且还将促进新型治疗剂的生产和/或使用以治疗使人类疾病衰弱的治疗。 公共卫生相关性：该提案将研究合作蛋白 - 蛋白质相互作用如何控制无处不在表达的衔接蛋白GRB2的SH2和SH3域的特异性和结合能力。从这项研究中获得的知识将有助于我们了解GRB2和其他相关临床上重要的蛋白质的激活和功能，这将为这些蛋白质的合理设计和/或使用抑制剂提供关键信息。这些药物将有助于治疗多种人类疾病，包括癌症，心血管疾病，自身免疫性疾病，哮喘/过敏以及移植器官的排斥。