Engineering the Met receptor: a potent antagonist of tumor growth and metastasis

改造 Met 受体：肿瘤生长和转移的有效拮抗剂

• 批准号: 7539905
• 负责人: JENNIFER R COCHRAN
• 金额: $ 16.89万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-12-10 至 2010-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7539905
• 关键词: Address; Affinity; Basic Science; Binding; Biochemistry; Biological; Biological Process; Biology; Boxing; Breast; Cell Line; Cell Proliferation; Cell surface; Cells; Chronic Myeloid Leukemia; Clinical; Complex; Diagnostic; Dimerization; Embryonic Development; Engineering; Epidermal Growth Factor Receptor; Evaluation; Evolution; Exhibits; Exploratory/Developmental Grant; Extracellular Domain; Flow Cytometry; Flowcharts; Future; Goals; Health; Hepatocyte Growth Factor; Human; Invaded; Laboratories; Length; Libraries; Ligand Binding; Ligands; Lung; MAP Kinase Gene; Malignant Epithelial Cell; Malignant Neoplasms; Mammalian Cell; Measures; Mediating; Methods; Mission; Modeling; Molecular; Molecular and Cellular Biology; Mus; Neoplasm Metastasis; Oncogenes; Pathogenesis; Pathologic Processes; Phenotype; Phosphorylation; Phosphotransferases; Plant Roots; Play; Positioning Attribute; Process; Property; Protein Engineering; Protein Tyrosine Kinase; Proteins; Proto-Oncogene Protein c-met; Proto-Oncogenes; Receptor Protein-Tyrosine Kinases; Recombinants; Research; Role; SHFM1 gene; Screening procedure; Signal Pathway; Signal Transduction; Signaling Molecule; Solid; Stomach Carcinoma; Suppressor Genes; Surface; System; Technology; Testing; Therapeutic; Therapeutic Intervention; Time; Western Blotting; Work; Yeasts; base; cancer cell; cancer therapy; cell type; combinatorial; directed evolution; high risk; improved; insight; interest; malignant breast neoplasm; meetings; microbial; migration; molecular imaging; multidisciplinary; mutant; neoplastic cell; prevent; protein expression; receptor; response; skills; tumor; tumor growth; tumorigenesis

DESCRIPTION (provided by applicant): The Met receptor tyrosine kinase is critical for mediating cell proliferation, survival and migration. The tendency for human tumors to invade and metastasize has been tied to the dysregulation of Met; therefore, Met is an extremely attractive target for therapeutic intervention. Interestingly, soluble Met extracellular domain (Met-ECD) acts as a potent antagonist of Met activation. Unfortunately, current methods for recombinant expression of Met-ECD have low yield, preventing both the full characterization of its biology and its deployment as a potential therapeutic. Our lab has robust and proven technology for the evolution, optimization, and expression of such challenging proteins, and Met-ECD is an ideal candidate for applying this technology. This work will accelerate biophysical characterization of Met ligand/receptor interactions, and applications of the Met receptor in cancer therapy and diagnostics. Aim 1: Engineer the full-length Met extracellular domain for high soluble expression levels in yeast. Directed evolution using yeast surface display provides us with a robust combinatorial platform to identify Met- ECD mutants that 1) possess the native receptor fold and 2) exhibit high soluble expression levels (mg/L) in yeast. Aim 2: Measure the ligand binding affinity and biological activity mediated by Met-ECD mutants. We will test the Met-ECD mutants isolated in Aim 1 to verify that engineered receptors with improved expression retain native ligand binding properties and biological function. We will fuse Met-ECD mutants to wild-type Met transmembrane and intracellular domains, and transfect these constructs into a mammalian cell line that expresses low levels of endogenous Met. We will test these cells lines for their ability to bind HGF ligand and induce cell signaling, comparing them to cells transfected with wild-type Met. These efforts will demonstrate the biological functions of Met-ECD mutants, validating them for future biophysical studies. Aim 3: Determine the ability of soluble Met-ECD mutants to bind to tumor cells and inhibit signaling. We will determine if soluble Met-ECD mutants function as receptor antagonists by measuring their ability to 1) bind to Met-expressing tumor cells and 2) inhibit ligand-dependent and ligand-independent activation of the Met kinase domain and downstream MAPK and PI3K signaling pathways. This Aim will validate Met-ECD mutants as receptor antagonists in a variety of cell types and motivate future research into their therapeutic potential. Project Narrative The availability of functional recombinant Met-ECD will profoundly impact future research into mechanisms of tumorigenesis, bacterial pathogenesis, and embryonic development, and will provide insight into how these processes can be manipulated. The fact that the Met-ECD itself could also be developed for applications in molecular imaging or cancer therapy is another example of this project's high impact.

描述（由申请方提供）：Met受体酪氨酸激酶对于介导细胞增殖、存活和迁移至关重要。人类肿瘤侵袭和转移的趋势与Met的失调有关;因此，Met是治疗干预的极具吸引力的靶标。有趣的是，可溶性Met胞外结构域（Met-ECD）作为Met活化的有效拮抗剂。不幸的是，目前用于重组表达Met-ECD的方法具有低产量，这妨碍了其生物学的完全表征及其作为潜在治疗剂的部署。我们的实验室拥有强大且经过验证的技术，可用于此类具有挑战性的蛋白质的进化，优化和表达，Met-ECD是应用该技术的理想候选人。这项工作将加速Met配体/受体相互作用的生物物理表征，以及Met受体在癌症治疗和诊断中的应用。目的1：工程化全长Met胞外结构域以在酵母中高可溶性表达水平。使用酵母表面展示的定向进化为我们提供了一个稳健的组合平台来鉴定1）具有天然受体折叠和2）在酵母中表现出高可溶性表达水平（mg/L）的Met-ECD突变体。目的2：测定Met-ECD突变体介导的配体结合亲和力和生物学活性。我们将测试在目标1中分离的Met-ECD突变体，以验证具有改善的表达的工程化受体保留天然配体结合特性和生物学功能。我们将Met-ECD突变体融合到野生型Met跨膜和细胞内结构域，并将这些构建体转染到表达低水平内源性Met的哺乳动物细胞系中。我们将测试这些细胞系结合HGF配体和诱导细胞信号传导的能力，并将其与野生型Met转染的细胞进行比较。这些努力将证明Met-ECD突变体的生物学功能，为未来的生物物理研究验证它们。目的3：确定可溶性Met-ECD突变体结合肿瘤细胞并抑制信号传导的能力。我们将通过测量可溶性Met-ECD突变体1）与表达Met的肿瘤细胞结合和2）抑制Met激酶结构域和下游MAPK和PI 3 K信号通路的配体依赖性和配体非依赖性活化的能力，确定其是否作为受体拮抗剂发挥作用。这一目标将验证Met-ECD突变体作为受体拮抗剂在各种类型的细胞，并激发未来的研究，以其治疗潜力。功能性重组Met-ECD的可用性将深刻影响未来对肿瘤发生，细菌发病机制和胚胎发育机制的研究，并将提供如何操纵这些过程的见解。Met-ECD本身也可以开发用于分子成像或癌症治疗，这一事实是该项目高影响力的另一个例子。