Molecular aspects of copper binding to the prion protein

描述(申请人提供)：本研究计划的目标是在分子水平上阐明PrP中铜和锌结合的机制和功能，以及这些相互作用与神经元维护和神经疾病的关系。Prion蛋白(PrP)的一种错误折叠形式导致了一类被称为可传播海绵状脑病(TSE)的致命神经退行性疾病，其中包括人类的疯牛病和克雅氏病。PRP是一种高度丰富的膜结合糖蛋白，存在于所有哺乳动物和鸟类中。虽然PrP最初被认为在神经退行性疾病中发挥作用，但现在很清楚，PrP对于维持神经元功能和调节细胞凋亡是必不可少的。PrP在对PrP活性至关重要的部位同时吸收铜和锌。在过去的资助期间，PI的实验室表征了这些金属离子位置的结构和热力学特征，并确定了某些突变与遗传性Pron病的发病年龄之间的显著联系。下一个资助期将以这些发现为基础，利用磁共振和细胞研究进行以下项目：1)确定全长、铜或锌占据的蛋白质的结构；2)评估金属离子如何影响体内的裂解，与细胞凋亡调控有关；以及3)检查与遗传病相关的突变以及预防疾病的突变如何改变结构和细胞行为。此外，项目三将应用新的合成策略来研究蛋白质糖基化的作用。预计这些研究将为理解PrP和铜在基础神经化学中的作用以及治疗神经退行性疾病和脑创伤的策略提供基本的新概念。 与公共健康相关：这项研究旨在评估中枢神经系统中调节铜和其他微量营养素的蛋白质。这些蛋白质对神经元健康至关重要，了解它们的行为将导致治疗阿尔茨海默氏症等神经退行性疾病和治疗脑创伤的新策略。

DESCRIPTION (provided by applicant): The objective of this research program is to elucidate, at the molecular level, the mechanism and function of copper and zinc binding in the prion protein (PrP) and the relationship of these interactions to neuron maintenance and neurological disease. A misfolded form of the prion protein (PrP) is responsible for a class of fatal neurodegenerative diseases termed the Transmissible Spongiform Encephalopathies (TSEs), which include mad cow disease and Creutzfeldt-Jakob disease in humans. PrP is a highly abundant, membrane-bound glycoprotein found in all mammals and avian species. Although originally recognized for its role in neurodegenerative disease, it is now clear that PrP is essential for sustaining neuron function and regulating apoptosis. PrP takes up both copper and zinc at sites are essential for PrP activity. Over the last funding period, the PI's laboratory characterized structural and thermodynamic features of these metal ion sites and also identified a remarkable link between certain mutations and onset age in inherited prion disease. The next funding period will build on these findings using both magnetic resonance and cellular studies with the following projects: 1) determine the structure of the full-length, copper or zinc occupied protein; 2) evaluate how metal ions influence in vivo cleavage, implicated in apoptosis regulation; and 3) examine how structure and cellular behavior is altered by mutations associated with inherited disease, and also by mutations that prevent disease. Moreover, project three will apply new synthetic strategies for investigating the role of protein glycosylation. It is anticipated that these studies will provide fundamental new concepts for understanding the role of both PrP and copper in basic neurochemistry, and strategies for treating neurodegenerative disease and brain trauma. PUBLIC HEALTH RELEVANCE: This research is aimed at evaluating proteins of the central nervous system that regulate copper and other micronutrients. These proteins are essential for neuron health and understanding their behavior will lead to new strategies for treating neurodegenerative diseases, such as Alzheimer's, and treating brain trauma.