Biochemical and Functional Analysis of Trypanin

锥虫蛋白酶的生化和功能分析

• 批准号: 7746404
• 负责人: KENT L HILL
• 金额: $ 36.96万
• 依托单位: UNIVERSITY OF CALIFORNIA LOS ANGELES
• 依托单位国家: 美国
• 财政年份: 2002
• 资助国家: 美国
• 起止时间: 2002-06-01 至 2013-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7746404
• 关键词: Abbreviations; Address; African; African Trypanosomiasis; Binding; Biochemical; Blood Circulation; Blood Vessels; Cell Communication; Cell division; Cell-Matrix Junction; Cells; Cellular biology; Cilia; Co-Immunoprecipitations; Communicable Diseases; Complex; Cytokinesis; Defect; Development; Disease; Drug Delivery Systems; Dynein ATPase; Endothelium; Epilepsy; Equipment and supply inventories; Eukaryota; Eye diseases; Flagella; Fractionation; Genes; Genetic; Genomics; Goals; Hereditary Disease; Human; Human body; Hydrocephalus; Immigration; Immune; Immunoglobulins; In Situ; Infertility; Insect Vectors; Left; Length; Life Cycle Stages; Link; Malaria; Mediating; Membrane; Modeling; Molecular; Morbidity - disease rate; Morphogenesis; Neuraxis; Obesity; Organelles; Organism; Parasites; Pathogenesis; Penetration; Phenotype; Polycystic Kidney Diseases; Proteins; Proteomics; RNA Interference; Research; Role; Sensory; Series; Signal Transduction Pathway; Site; Site-Directed Mutagenesis; Staging; Structural Protein; Structure; Surface Antigens; Testing; Therapeutic Intervention; Tissues; Trypanosoma; Trypanosoma brucei brucei; Tsetse Flies; cell motility; disease transmission; dynein light chain; economic impact; extracellular; health economics; human disease; migration; mortality; mutant; neuronal cell body; pathogen; public health relevance; three dimensional structure; tomography

DESCRIPTION (provided by applicant): African trypanosomes (e.g. Trypanosoma brucei) are protozoan parasites that cause African sleeping sickness, a fatal disease with devastating health and economic impact. These parasites are digenetic organisms, spending part of their life cycle in a mammalian host and part in an insect vector (the tsetse fly). Trypanosomes are highly motile in both life cycle stages and motility is central to parasite development and disease pathogenesis. Motility is mediated by a single flagellum that is an essential and multifunctional organelle with critical roles in cell motility, host-parasite interaction, cell morphogenesis and cell division. Surprisingly, we know very little about the flagellar apparatus at the molecular level. In particular, we lack an understanding of how flagellar proteins are assembled into supramolecular structures within the axoneme and how they function individually and collectively to drive cell motility and other flagellum functions. The long-term goal of the proposed research is to advance our understanding of the trypanosome flagellum and to exploit trypanosomes as a model to investigate the eukaryotic cilium. This will be done using a combination of functional and structural approaches. RNAi, site-directed mutagenesis and ultrastructural analyses will be used to investigate the function of trypanin and other components of the dynein regulatory complex (DRC). The DRC is part of a signal transduction pathway that regulates flagellar motility and is essential in bloodstream-form trypanosomes, making it a candidate drug target. The trypanosome flagellum is analogous to cilia and flagella in other eukaryotes, including humans. Flagella are required for motility of several human pathogens and are present on most tissues of the human body. They perform motility, transport and sensory functions. Infectious diseases caused by pathogens that require cilia include African sleeping sickness and Malaria. Together, these diseases are responsible for mortality and morbidity in approximately 0.4 billion people world-wide. Heritable human diseases caused by cilia defects include: hydrocephalus, infertility, epilepsy, left-right axis defects, eye disorders, polycystic kidney disease and obesity. Therefore, in addition to addressing fundamental questions in cell biology, this research directly impacts efforts to understand and treat infectious diseases and genetic diseases in humans. PUBLIC HEALTH RELEVANCE: African trypanosomes are protozoan parasites that cause African sleeping sickness, a fatal disease with devastating health and economic impact. The trypanosome flagellum is essential for viability and is central to parasite development and disease pathogenesis. Therefore, this research will directly impact efforts to understand and treat infectious human disease.

描述（由申请方提供）：非洲锥虫（例如布氏锥虫）是一种原生动物寄生虫，可引起非洲昏睡病，这是一种致命疾病，对健康和经济造成毁灭性影响。这些寄生虫是二代生物，其生命周期的一部分在哺乳动物宿主中度过，一部分在昆虫载体（采采蝇）中度过。锥虫在两个生命周期阶段都是高度能动的，能动性是寄生虫发育和疾病发病机制的核心。运动是由一个单一的鞭毛，这是一个重要的和多功能的细胞器，在细胞运动，宿主-寄生虫的相互作用，细胞形态发生和细胞分裂的关键作用。令人惊讶的是，我们在分子水平上对鞭毛器知之甚少。特别是，我们缺乏对鞭毛蛋白如何组装成轴丝内的超分子结构以及它们如何单独和集体地驱动细胞运动和其他鞭毛功能的理解。该研究的长期目标是促进我们对锥虫鞭毛的理解，并利用锥虫作为研究真核纤毛的模型。这将使用功能和结构方法相结合来完成。RNAi、定点突变和超微结构分析将用于研究锥蛋白和动力蛋白调节复合物（DRC）的其他组分的功能。DRC是调节鞭毛运动的信号转导途径的一部分，并且在血流形式的锥虫中是必需的，使其成为候选药物靶标。锥虫鞭毛类似于其他真核生物（包括人类）的纤毛和鞭毛。鞭毛是几种人类病原体运动所必需的，并且存在于人体的大多数组织上。它们执行运动、运输和感觉功能。由需要纤毛的病原体引起的传染病包括非洲昏睡病和疟疾。这些疾病加在一起造成全世界约4亿人的死亡和发病。由纤毛缺陷引起的遗传性人类疾病包括：脑积水、不育、癫痫、左右轴缺陷、眼部疾病、多囊肾病和肥胖症。因此，除了解决细胞生物学中的基本问题外，这项研究还直接影响了理解和治疗人类传染病和遗传病的努力。公共卫生关系：非洲锥虫是一种原生动物寄生虫，会引起非洲昏睡病，这是一种致命的疾病，对健康和经济造成毁灭性的影响。锥虫鞭毛是生存所必需的，是寄生虫发育和疾病发病机制的核心。因此，这项研究将直接影响理解和治疗人类传染病的努力。