Understanding and Controlling Protein Aggregation and Disease: Molecular Mechanisms in vitro and in vivo

背景尽管淀粉样蛋白疾病（包括帕金森氏症和阿尔茨海默氏症）在我们老龄化人口中的重要性日益增加，但我们缺乏关于蛋白质聚集如何以及为什么会导致疾病的基本知识。需要这些知识来制定针对这些与年龄有关的疾病的成功治疗策略。目的在这个项目中，我们将集中在一个新发现的β 2-微球蛋白（β 2 m）的变异，导致致命的系统性淀粉样变性。我们将确定这种突变体聚集的方式和原因;生成并表征秀丽隐杆线虫beta2 m疾病模型，并筛选能够防止其聚集的小分子。然后，我们将确定小分子在体外防止聚集的作用机制，并利用秀丽隐杆线虫作为一个强大的模型system.NoveltyIn最近的工作，我们已经设计了一种新的和强大的屏幕在大肠杆菌中识别小分子，防止蛋白质聚集测试其在活的生物体中的功效。我们将利用我们的合作者理查德·福斯特提供的一个重新利用的小分子库，（化学学院），并筛选它们在完整的活动物中增强蛋白质稳态的功效和潜力。及时性结合利用秀丽隐杆线虫作为活生物体中小分子命中功效的筛选，该项目不仅将为博士生提供良好的培训，而且还将产生具有基础和转化重要性的新知识。实验方法该项目将生物化学，蛋白质化学，结构生物学和生物物理学与体内分析和高通量筛选方法使用秀丽隐杆线虫。所需的所有方法和途径都已在申请人的实验室中确立。因此，学生将获得各种方法的优秀培训，并将其应用于一个令人兴奋的多学科项目，该项目可在该博士的4年任期内实现。

BackgroundDespite the increasing importance of amyloid diseases including Parkinson's and Alzheimer's in our ageing population, we lack fundamental knowledge about how and why protein aggregation causes disease. Such knowledge is needed to develop successful therapeutic strategies against these age-related diseases. ObjectivesIn this project we will focus on a newly identified variant of beta2-microglobulin (beta2m) that causes fatal systemic amyloidosis. We will determine how and why this mutant aggregates; generate and characterize a C.elegans beta2m-disease model and screen for small molecules able to prevent its aggregation. We will then determine the mechanism of action of the small molecules in preventing aggregation in vitro and test their efficacy in a living organism exploiting C.elegans as a powerful model system.NoveltyIn recent work we have devised a novel and powerful screen in E.coli to identify small molecules that prevent protein aggregation. We will use this for a recently identified amyloid disease using a library of repurposed small molecules provided by our collaborator Richard Foster (School of Chemistry), and screen their efficacy and potential to enhance proteostasis in an intact living animal.TimelinessCombined with the exploitation of C.elegans as a screen for efficacy of small molecule hits in a living organism, the project will not only provide excellent training for a PhD student but it will also result in new knowledge of both fundamental and translational importance.Experimental approachThe project combines biochemistry, protein chemistry, structural biology and biophysics with in vivo analyses and high-throughput screening methodologies using C.elegans. All methods and approaches needed are already well established in the applicants' laboratories. Hence the student will obtain excellent training in a wide variety of methods and will apply them to an exciting multidisciplinary project that is achievable within the 4 year tenure of this PhD.