Role of the Shp-2 tyrosine phosphatase in signal transdu

Shp-2 酪氨酸磷酸酶在信号转导中的作用

• 批准号: 6911072
• 负责人: Gen-Sheng Feng
• 金额: $ 14.33万
• 依托单位: SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE
• 依托单位国家: 美国
• 财政年份: 1996
• 资助国家: 美国
• 起止时间: 1996-03-01 至 2005-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6911072
• 关键词: biological signal transduction; cell growth regulation; cell transformation; cell type; enzyme activity; epidermal growth factor; extracellular matrix; genetically modified animals; growth factor receptors; immunoaffinity chromatography; immunoprecipitation; laboratory mouse; mitogen activated protein kinase; northern blottings; phosphorylation; polymerase chain reaction; protein structure function; protein tyrosine kinase; protein tyrosine phosphatase; tissue /cell culture; western blottings

Reversible tyrosine phosphorylation, a major biochemical event in cell regulation, is controlled by the opposing activities of protein tyrosine kinases (PTKs) and protein tyrosine phosphatases (PTPs). However, relatively little is known about the mechanism for regulation and functions of PTPs, as compared to the extensive attention received for PTKs. The goal of this project is to determine the role of Shp-2, a PTP with two src-homology 2 (SH2) domains, in intracellular signal transduction. Work from this laboratory and others implicates the involvement of Shp-2 in different signaling pathways as a positive or a negative regulator in the control of cell growth, differentiation, migration and death. In particular, Shp-2 acts to promote growth factor stimulation of extracellular signal regulated kinase (ERK) activity. However, it remains a mystery how a PTP can act positively downstream of a receptor PTK to enhance the induction of ERK activity. Our most recent data present a fresh view that Shp-2 works in concert with Gab1 scaffold protein in a multimeric protein complex, in promoting the activation of the Ras-Raf-MEK-ERK cascade by epidermal growth factor. In this competitive renewal of the previously funded R29 grant, we propose to determine the biochemical basis for Shp-2 function in Ras-ERK activation by identifying its specific substrate(s). We will further investigate the physiological role of Shp-2 in cytoplasmic signaling, particularly in the modulation of information flow along the Ras pathway, and we will also determine the phosphatase-dependent and independent activities of the Shp-2 protein. Finally, we will define the biological function of Shp-2 in different cell types. Results from this study will allow us understand better how PTPs are regulated and how PTP activities are executed during intracellular signal relay in general.

可逆的酪氨酸磷酸化是细胞调节中的一个主要生化事件，由蛋白质酪氨酸激酶（PTK）和蛋白质酪氨酸磷酸酶（PTPs）的相反活性控制。 然而，相对于PTKs受到的广泛关注，PTPs的调控机制和功能知之甚少。 本项目的目的是确定Shp-2，一个PTP与两个src同源2（SH 2）结构域，在细胞内信号转导中的作用。 该实验室和其他实验室的工作暗示Shp-2参与不同的信号传导途径，作为控制细胞生长、分化、迁移和死亡的正或负调节剂。 特别地，Shp-2起促进生长因子刺激细胞外信号调节激酶（ERK）活性的作用。 然而，PTP如何在受体PTK下游积极作用以增强ERK活性的诱导仍然是一个谜。 我们最近的数据提出了一个新的观点，Shp-2与Gab 1支架蛋白在多聚体蛋白复合物中协同工作，促进表皮生长因子激活Ras-Raf-MEK-ERK级联反应。 在先前资助的R29补助金的竞争性更新中，我们建议通过确定其特定底物来确定Ras-ERK激活中Shp-2功能的生化基础。 我们将进一步研究Shp-2在细胞质信号传导中的生理作用，特别是在Ras通路沿着的信息流的调节中，我们还将确定Shp-2蛋白的磷酸酶依赖性和独立性活性。 最后，我们将确定Shp-2在不同细胞类型中的生物学功能。 这项研究的结果将使我们更好地了解PTP是如何调节的，以及PTP活动是如何在细胞内信号传递过程中执行的。