Redox Regulation of DJ-1 Function

DJ-1 功能的氧化还原调节

• 批准号: 8118584
• 负责人: Mark A. Wilson
• 金额: $ 26.76万
• 依托单位: UNIVERSITY OF NEBRASKA LINCOLN
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-08-01 至 2015-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8118584
• 关键词: Affect; Affinity; Aging-Related Process; Animal Model; Animals; Apoptosis; Binding; Biochemical; Biochemistry; Biological Models; Cell Culture Techniques; Cells; Communities; Complement; Cysteine; Cytoprotection; Data; Disease; Drosophila genus; Drosophila melanogaster; Escherichia coli; Etiology; Eukaryota; Generations; Genetic; Goals; Homeostasis; Homologous Gene; Human; Knock-out; Knowledge; Lead; Maintenance; Malignant Neoplasms; Messenger RNA; Mitochondria; Modification; Molecular; Mutation; Neurodegenerative Disorders; Organism; Oxidation-Reduction; Oxidative Regulation; Oxidative Stress; PARK7 protein; Parkinsonian Disorders; Pathogenesis; Play; Post-Translational Protein Processing; Prokaryotic Cells; Protein Family; Proteins; Proteome; Publications; RNA Binding; Regulation; Research; Roentgen Rays; Role; Scientist; Stroke; Structure; Structure-Activity Relationship; System; Testing; Therapeutic; Transcript; Translations; Work; X-Ray Crystallography; base; biological adaptation to stress; cell type; cysteine sulfinic acid; design; effective therapy; expectation; experience; human disease; improved; in vivo; innovation; insight; macromolecule; member; mitochondrial dysfunction; oxidation; protein function; public health relevance; sensor; therapy development

DESCRIPTION (provided by applicant): Oxidative stress and mitochondrial dysfunction are centrally involved in the etiology of several diseases and in the normal process of aging. The protein DJ-1 is an oxidative stress response protein whose absence or dysregulation has been implicated in parkinsonism, cancer, and stroke. DJ-1 can robustly protect cells against multiple forms of oxidative stress and thereby confer protection against degeneration that can lead to disease. The molecular mechanism(s) of DJ-1's action, however, remains unclear. DJ-1 contains a functionally essential cysteine residue whose oxidation is hypothesized to regulate its cytoprotective function. We will investigate the mechanism by which DJ-1 senses and responds to oxidative stress by accomplishing three specific aims. The first aim will investigate the role of DJ-1 cysteine oxidation in the protection against oxidative stress in the Drosophila animal model system. We will combine X-ray crystallography, biochemistry, and Drosophila genetics to establish a powerful animal model for the redox regulation of DJ-1 function. The second aim will determine the structure-function relationships for an established mRNA binding activity of DJ-1. The results will be used to test the hypothesis that conserved structural features near the oxidized cysteine integrate the RNA binding and redox sensing functions of DJ-1. The third aim will use a prokaryotic model system to investigate the evolutionarily conserved mechanism of DJ-1 protective function. The results will be used to test existing hypotheses about the conservation of regulatory cysteine oxidation in DJ-1 function as well as discover new functions for DJ-1. In total, the proposed research will provide a comprehensive molecular basis for understanding the oxidative regulation and pathogenic disruption of DJ-1 function. Ultimately, the results of this research will be used to design a new generation of therapeutics that enhance the protective function of DJ-1 in vulnerable cell types. PUBLIC HEALTH RELEVANCE: Oxidative stress and mitochondrial dysfunction are centrally involved in several human diseases. Major recent advances have identified DJ-1 as a protein that confers robust protection against oxidative stress. The precise biochemical function of DJ-1, however, remains uncertain. The long-term goal of this proposal is to determine the biochemical functions of DJ-1 that confer protection against oxidative stress and with the goal of developing therapies that improve the protective function of DJ-1.

描述(申请人提供)：氧化应激和线粒体功能障碍与几种疾病的病因和正常的衰老过程密切相关。DJ-1蛋白是一种氧化应激反应蛋白，其缺失或失调与帕金森氏症、癌症和中风有关。DJ-1可以有力地保护细胞免受多种形式的氧化应激，从而防止可能导致疾病的退化。然而，DJ-1‘S作用的分子机制(S)尚不清楚。DJ-1含有一个功能必需的半胱氨酸残基，其氧化被假设为调节其细胞保护功能。我们将通过实现三个特定的目标来研究DJ-1感知和响应氧化应激的机制。第一个目的是在果蝇动物模型系统中研究DJ-1半胱氨酸氧化在保护果蝇免受氧化应激中的作用。我们将结合X射线结晶学、生物化学和果蝇遗传学，为DJ-1功能的氧化还原调节建立一个强大的动物模型。第二个目的将确定DJ-1已建立的mRNA结合活性的结构-功能关系。这些结果将被用来检验这一假设，即氧化半胱氨酸附近的保守结构特征整合了DJ-1的RNA结合和氧化还原传感功能。第三个目的是利用原核模型系统来研究DJ-1保护功能的进化保守机制。这些结果将被用来检验现有的关于DJ-1功能中调节半胱氨酸氧化保守的假说，以及发现DJ-1的新功能。总之，拟议的研究将为理解DJ-1功能的氧化调节和致病破坏提供全面的分子基础。最终，这项研究的结果将被用于设计新一代疗法，以增强DJ-1对脆弱细胞类型的保护功能。 公共卫生相关性：氧化应激和线粒体功能障碍与几种人类疾病密切相关。最近的重大进展已经确定DJ-1是一种蛋白质，可以提供强大的氧化应激保护。然而，DJ-1的确切生化功能仍然不确定。这项建议的长期目标是确定DJ-1对氧化应激具有保护作用的生化功能，并旨在开发提高DJ-1保护功能的治疗方法。