Proteomics and Post-translational Modification

蛋白质组学和翻译后修饰

• 批准号: 10172233
• 负责人: Nicolas L Young
• 金额: $ 40.79万
• 依托单位: BAYLOR COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-06-01 至 2026-02-28
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10172233
• 关键词: Acetyl Coenzyme A; Age; Aging; Alzheimer' s Disease; Atlases; Biochemical; Biogenesis; Biology; Biology of Aging; Cell Nucleus; Cells; Chromatin; Communities; Complement; Computer Analysis; Data; Data Analyses; Development; Digestion; Disease; Epigenetic Process; Epitopes; Event; Functional disorder; Gene Expression; Gene Proteins; Genes; Genetic Transcription; Goals; Hippocampus (Brain); Histones; Homeostasis; Label; Lysosomes; Measures; Mediating; Metabolic; Methods; Molecular; Multiomic Data; Mus; Mutation; Nuclear; Organelles; Peptides; Post Translational Modification Analysis; Post-Translational Protein Processing; Program Research Project Grants; Protein Isoforms; Proteins; Proteolysis; Proteolytic Processing; Proteome; Proteomics; Regulation; Regulator Genes; Reproducibility; Research; Research Project Grants; Sampling; Signal Transduction; Specificity; Statistical Data Interpretation; System; Tauopathies; Transcriptional Regulation; Trypsin; Validation; Variant; Work; Writing; base; cost effective; histone modification; innovation; insight; lysosomal proteins; metabolome; metabolomics; programs; protein expression; proteostasis; single molecule; synergism; tool

Abstract Lysosomes are highly specialized and dynamic cellular organelles that help maintain protein homeostasis. Lysosomes also act as a signaling center of the cell. Many of these signals are transduced to the nucleus and ultimately modulate transcription of genes and the expression of protein products. This includes genes and proteins that are essential to lysosome function and biogenesis. Dysregulation of lysosomal genes and the dysfunction of the lysosome system are associated with aging and age-associated diseases, including Alzheimer’s disease. The Proteomics and Quantitative Post-translational Modification core (proteomics core) (Core B) will support all three research projects in this PPG proposal to elucidate changes in the proteome and the mechanisms by which protein expression is altered during aging and Alzheimer’s disease. We will use methods as described in our preliminary data to measure changes in (1) the lysosomal proteome, including isoforms and post-translational modifications, (2) post translational modifications in lysosome-associated signaling events upstream of transcription, and (3) histone post-translational modifications in lysosomal gene regulatory mechanisms. The proteomics core will leverage our expertise and current capacity in the proteomic analysis of subcellular organelles, targeted proteomic characterization and quantitation of protein modification state (proteoforms), as well as extensive expertise in signal transduction and histone modifications. The focus of Core B is to provide reproducible quantitation and detailed characterization of the lysosome and crucial proteins that are essential to the regulation of lysosomal biology in aging and tauopathy. This level of molecular detail is important because protein attributes, such as isoforms, proteolysis, and post-translational modifications, often function in concert or in specific hierarchies to execute their core function. Together, these studies will provide unparalleled detailed characterization that reveal molecular mechanisms of lysosome function, regulation, and biogenesis in aging biology, and Alzheimer’s disease pathophysiology. Core B will also actively collaborate with other Cores and Projects to create a first-in- class Aging- and Tauopathy-associated Lysosomal atlas (ATLas) of the lysosomal proteome and metabolome for mouse cortex and hippocampus to be shared with the general research community.

摘要 溶酶体是高度特化和动态的细胞器，有助于维持蛋白质稳态。 溶酶体也是细胞的信号中心。这些信号中的许多被转导到细胞核， 最终调节基因的转录和蛋白质产物的表达。这包括基因和 对溶酶体功能和生物发生至关重要的蛋白质。溶酶体基因的失调和 溶酶体系统的功能障碍与衰老和年龄相关疾病有关，包括 老年痴呆症蛋白质组学和定量翻译后修饰核心（蛋白质组学 核心）（核心B）将支持本PPG提案中的所有三个研究项目，以阐明 蛋白质组和蛋白质表达在衰老和阿尔茨海默病期间改变的机制。 我们将使用我们的初步数据中描述的方法来测量（1）溶酶体的变化， 蛋白质组，包括异构体和翻译后修饰，（2）翻译后修饰， 溶酶体相关的转录上游信号事件，和（3）组蛋白翻译后 溶酶体基因调控机制的改变。蛋白质组学核心将利用我们的专业知识 和亚细胞器的蛋白质组学分析的电流能力，有针对性的蛋白质组学表征 和蛋白质修饰状态（蛋白质形式）的定量，以及信号转导方面的广泛专业知识， 转导和组蛋白修饰。核心B的重点是提供可重现的定量和详细的 溶酶体和关键蛋白质的表征是必不可少的调节溶酶体生物学， 老化和tau蛋白病。这种分子细节水平很重要，因为蛋白质属性，如同种型， 蛋白质水解和翻译后修饰通常协同作用或在特定的层次结构中执行 其核心功能。总之，这些研究将提供无与伦比的详细表征，揭示 衰老生物学中溶酶体功能、调节和生物发生的分子机制，以及阿尔茨海默氏症 疾病病理生理学核心B还将积极与其他核心和项目合作， 溶酶体蛋白质组和代谢组的衰老和Tau病相关溶酶体图谱（ATLas） 用于小鼠皮层和海马体与一般研究团体共享。