Regulation of insulin-like growth factors by the ER chaperone GRP94

ER 伴侣 GRP94 对胰岛素样生长因子的调节

• 批准号: 8469513
• 负责人: YAIR ARGON
• 金额: $ 30.65万
• 依托单位: CHILDREN'S HOSP OF PHILADELPHIA
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-06-01 至 2015-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8469513
• 关键词: ATP phosphohydrolase; Affect; Anabolism; Apoptotic; Binding; Biochemical; Biological; Biological Assay; Calcium; Calcium Binding; Cells; Chimeric Proteins; Client; Clinical; Co-Immunoprecipitations; Code; Complement; Embryonic Development; Endoplasmic Reticulum; Essential Amino Acids; Family; Genes; Genetic Polymorphism; Genotype; Growth; Growth Factor; Growth Factor Interaction; Heat-Shock Proteins 90; Human; Hydrolysis; Individual; Insulin; Insulin-Like Growth Factor II; Lead; Light; Maps; Measures; Mediating; Metabolic stress; Molecular; Molecular Chaperones; Molecular Conformation; Mutagenesis; Mutation; Peptides; Physiologic pulse; Population; Production; Protein Binding; Protein Family; Protein Isoforms; Proteins; Recombinant Proteins; Regulation; Relaxin; Resolution; Serum-Free Culture Media; Signal Transduction; Site; Site-Directed Mutagenesis; Somatomedins; Specificity; Structure; Surface; TLR4 gene; Testing; Tissues; Transfection; Variant; Work; base; cell growth; embryonic stem cell; glucose-regulated protein 94; mutant; novel; patient population; preference; protein function; public health relevance; receptor; response

DESCRIPTION (provided by applicant): Insulin-like growth factors (IGFs) mediate differentiation decisions during embryonic development, cell growth signaling and responses to metabolic stress. We found that the production of these important growth factors is dependent on the activity of the endoplasmic reticulum chaperone glucose regulate protein 94 (GRP94), which is essential for their biosynthesis. GRP94 is different from other molecular chaperones in its selectivity towards only a small number of client proteins, preference for late folding intermediates and the absence of any known co-factors. All these aspects suggest a unique mode of action for GRP94. This project will elucidate the enigmatic action cycle of GRP94 by taking advantage of cells whose growth depends on the GRP94-IGF axis. In our first aim we will use a novel cell-based assay to screen for mutants of GRP94 that do not support IGF-II production and thus define amino acids that are essential for this chaperone function. In Aim 2, we will determine whether these mutants are defective in general mechanistic aspects, such as ATP binding and hydrolysis or calcium binding, or whether the mutations define a client binding domain. We will also test the ability of GRP94 mutants to support clients other than IGF, to discover whether there are client-specific mutants. Our third aim is to understand how GRP94 recognizes IGF, by exploiting the structural similarities and differences among a set of insulin-like proteins. These studies will inform on the client selectivity of GRP94, which is currently not understood. Finally, we will take advantage of the clinical consequences of IGF deficiency to search for functionally important human GRP94 variants. Following on our finding that at least one such variant affects IGF production, we will genotype and sequence IGF-deficient patient populations to seek allelic GRP94 variants that may explain low IGF production. Together, these results will lead to a new understanding of how GRP94 chaperones client proteins.

描述（由申请人提供）：胰岛素样生长因子（IGF）介导胚胎发育期间的分化决定、细胞生长信号传导和对代谢应激的反应。我们发现这些重要生长因子的产生依赖于内质网伴侣葡萄糖调节蛋白94（GRP 94）的活性，GRP 94对它们的生物合成至关重要。GRP 94与其他分子伴侣的不同之处在于其仅对少数客户蛋白的选择性，对后期折叠中间体的偏好以及不存在任何已知的辅因子。所有这些方面表明GRP 94的独特作用模式。本项目将通过利用依赖于GRP 94-IGF轴生长的细胞来阐明GRP 94的神秘作用周期。在我们的第一个目标中，我们将使用一种新的基于细胞的测定来筛选不支持IGF-II产生的GRP 94突变体，从而确定这种伴侣蛋白功能所必需的氨基酸。在目标2中，我们将确定这些突变体是否在一般机制方面有缺陷，例如ATP结合和水解或钙结合，或者突变是否定义了客户端结合结构域。我们还将测试GRP 94突变体支持IGF以外的客户端的能力，以发现是否存在客户端特定的突变体。我们的第三个目标是了解GRP 94如何识别IGF，通过利用一组胰岛素样蛋白之间的结构相似性和差异。这些研究将告知GRP 94的客户端选择性，这是目前尚不了解的。最后，我们将利用IGF缺乏的临床后果来寻找功能重要的人类GRP 94变体。在我们发现至少一种这样的变异影响IGF产生之后，我们将对IGF缺陷患者群体进行基因分型和测序，以寻找可能解释低IGF产生的等位基因GRP 94变异。总之，这些结果将导致对GRP 94伴侣蛋白如何客户蛋白质的新理解。