Biophysical Studies of Amyloid Formation by Polypeptide Hormones

多肽激素形成淀粉样蛋白的生物物理学研究

• 批准号: 10302169
• 负责人: DANIEL P RALEIGH
• 金额: $ 30.74万
• 依托单位: STATE UNIVERSITY NEW YORK STONY BROOK
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-07-01 至 2025-06-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10302169
• 关键词: Address; Alzheimer' s Disease; Amino Acids; Amyloid; Amyloid Fibrils; Amyloidosis; Anti-Obesity Agents; Beta Cell; Biochemistry; Biological Assay; Biophysics; Cardiovascular system; Cell physiology; Cells; Cellular biology; Cessation of life; Clinical; Code; Collaborations; Complement; Complications of Diabetes Mellitus; Conflict (Psychology); Data; Dependence; Deposition; Development; Diabetes Mellitus; Disease; Disease Progression; Endocrine; Epidemic; Failure; Functional disorder; Funding; Goals; Hormone replacement therapy; Hormones; Human; Hydrogen Bonding; In Vitro; Individual; Insulin; Insulin-Dependent Diabetes Mellitus; Islet Cell; Islets of Langerhans; Islets of Langerhans Transplantation; Isotope Labeling; Link; Metabolic; Metabolic Diseases; Metabolic hormone; Methods; Molecular; Molecular Conformation; Mutation; Non-Insulin-Dependent Diabetes Mellitus; Obesity; Pancreas; Pathologic; Play; Polypeptide Hormones; Process; Proline; Proteins; Regulation; Research; Risk; Role; Scanning; Solubility; Structural Models; Structure; Structure of beta Cell of islet; Testing; Therapeutic Agents; Time; Toxic effect; United States; Variant; Work; amyloid formation; analog; autocrine; base; beta pleated sheet; biophysical analysis; cytotoxic; design; diabetes risk; glucose metabolism; insight; interest; islet; islet amyloid polypeptide; mutant; next generation; novel; obesity treatment; paracrine; preservation; programs; protein aggregation; proteotoxicity; therapeutic target; treatment strategy; type I and type II diabetes

PROJECT SUMMARY This application describes an interdisciplinary program designed to study amyloid formation by human islet amyloid polypeptide (hIAPP, also known as amylin), the causative agent of pancreatic islet amyloidosis-induced beta-cell toxicity in diabetes. Amyloid formation by hIAPP is a well-established pathological factor contributing to the development of type 2 diabetes, a debilitating disease that has reached epidemic proportions in the United States. Islet amyloidosis is also a major contributor to islet cell transplantation failure. Aggregation of hIAPP has recently been implicated in islet beta-cell deficiency in type 1 diabetes, and in the downstream cardiovascular complications of diabetes. hIAPP is normally secreted as a soluble polypeptide hormone together with insulin from the pancreatic beta-cells and plays an adaptive role in glucose metabolism, including the regulation of the action of insulin and other pancreatic metabolic hormones. However, in metabolic disease, hIAPP aggregates into cytotoxic conformations that assemble into amyloid fibrils that deposit as plaques in the islets. The process of islet amyloid formation is toxic to beta-cells and plays an important role in disease progression. Wild type hIAPP is responsible for islet amyloidosis in the majority of individuals, but an S20G mutation is linked to an increased risk of diabetes. Soluble analogs of hIAPP are of interest as adjuncts to insulin therapy for the treatment of diabetes, particularly for type 1 diabetes, where the rapid loss of beta-cells results in dependence on hormone replacement therapy. Soluble hIAPP analogs are also of interest for the potential treatment of obesity. The planned studies address fundamental issues in amyloid formation, and will offer important insight into strategies for the treatment of type 1 and type 2 diabetes. We will apply an interdisciplinary combination of protein biophysics, biochemistry, and islet cell biology to address three key issues in the field: 1) defining the determinates of hIAPP amyloid formation and toxicity, including the role of specific amino acid sidechain interactions; 2) elucidating the reasons for the aggressive aggregation and heightened toxicity of the S20G mutant of hIAPP; and 3) the rational development and rigorous testing of next generation soluble analogs of hIAPP. The studies will define the molecular features impacting hIAPP amyloid formation and islet beta-cell toxicity. They will identify general principles that will be broadly applicable to other protein aggregation diseases, and to mechanistic studies of amyloid formation.

项目摘要 本申请描述了一个跨学科的计划，旨在研究淀粉样蛋白的形成， 淀粉样多肽（hIAPP，也称为胰淀素），胰岛淀粉样变性诱导的胰腺炎的病原体， 糖尿病中的β细胞毒性。由hIAPP形成的淀粉样蛋白是一个公认的病理因素，有助于 2型糖尿病是一种使人衰弱的疾病，在美国已达到流行病的程度。 States.胰岛淀粉样变性也是胰岛细胞移植失败的主要原因。hIAPP的聚集具有 最近被认为与1型糖尿病的胰岛β细胞缺乏有关，并与下游心血管疾病有关。 糖尿病并发症hIAPP通常作为可溶性多肽激素与胰岛素一起分泌， 胰腺β细胞，并在葡萄糖代谢中起适应性作用，包括调节作用， 胰岛素和其他胰腺代谢激素。然而，在代谢性疾病中，hIAPP聚集成 细胞毒性构象，组装成淀粉样纤维，存款为胰岛中的斑块。的过程 胰岛淀粉样蛋白的形成对β细胞是有毒的，并在疾病进展中起重要作用。野生型hIAPP 在大多数个体中，S20 G突变是导致胰岛淀粉样变性的原因，但S20 G突变与胰岛淀粉样变性增加有关。 糖尿病的风险。hIAPP的可溶性类似物作为胰岛素疗法的替代物用于治疗糖尿病是令人感兴趣的。 糖尿病，特别是1型糖尿病，其中β细胞的快速损失导致对激素的依赖 替代疗法可溶性hIAPP类似物对于肥胖症的潜在治疗也是令人感兴趣的。的 计划中的研究解决淀粉样蛋白形成的基本问题，并将提供重要的洞察战略， 用于治疗1型和2型糖尿病。我们将运用跨学科的方法 生物物理学、生物化学和胰岛细胞生物学，以解决该领域的三个关键问题：1）定义 确定hIAPP淀粉样蛋白的形成和毒性，包括特定氨基酸侧链的作用 2）阐明了S20 G的侵袭性聚集和毒性增强的原因 hIAPP突变体;和3）下一代可溶性类似物的合理开发和严格测试 hIAPP。这些研究将确定影响hIAPP淀粉样蛋白形成和胰岛β细胞毒性的分子特征。 他们将确定广泛适用于其他蛋白质聚集疾病的一般原则， 淀粉样蛋白形成的机制研究。