Regulation and specificity of deubiquitylating enzyme complex

去泛素化酶复合物的调节和特异性

• 批准号: 8618909
• 负责人: Zhihao Zhuang
• 金额: $ 25.27万
• 依托单位: UNIVERSITY OF DELAWARE
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-05-01 至 2017-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8618909
• 关键词: Active Sites; Ataxia; Binding; Binding Sites; Biological Assay; C-terminal; Catalysis; Chemicals; Complex; Coupled; Crosslinker; Enzymes; Face; Family; Free Energy; Gel; Goals; Homologous Gene; Human; Human Ubiquitin; Intervention; Iodoacetamide; Kinetics; Knowledge; Link; Lysine; Malignant Neoplasms; Maps; Mass Spectrum Analysis; Modeling; Molecular; Molecular Conformation; Mono-S; Multienzyme Complexes; Mutation Analysis; N-terminal; Neurodegenerative Disorders; Pathogenesis; Phosphorylation; Physiological; Polyubiquitin; Positioning Attribute; Process; Proliferating Cell Nuclear Antigen; Protease Inhibitor; Protein Family; Proteins; Proteomics; Regulation; Serine; Site; Site-Directed Mutagenesis; Specificity; Structure; System; Tail; Testing; Therapeutic; Therapeutic Agents; Ubiquitin; Ubiquitin C; Virus Diseases; base; crosslink; design; gel electrophoresis; human disease; improved; insight; novel therapeutics; protein complex; protein function; ubiquitin ligase; ubiquitin-aldehyde; ubiquitin-specific protease

DESCRIPTION (provided by applicant): Abnormal regulation of human deubiquitylating enzymes (DUBs) has been implicated in the pathogenesis of a number of human diseases including cancer, neurodegenerative disorders and viral infection. Ubiquitin-specific proteases (USPs) constitute the largest family among the five known DUB families. Human USPs are emerging as promising targets for pharmacological intervention. However, the lack of understanding of the specificity and regulation of USPs has hindered the progress in developing novel therapeutics. Remarkably, a recent global proteomic analysis of human DUBs revealed that over thirty human USPs are associated specifically with WD40-repeat proteins. Given its widespread occurrence, the interaction between WD40- repeat proteins and USPs likely represents a fundamentally important way of regulating USP activity. This application focuses on a prototypical USP WD40-repeat protein complex, human USP1/UAF1, and its close homologs. The overarching goal of this application is to gain an in-depth understanding of the specificity and regulation of human USPs and the USP WD40-repeat protein complexes. There are three specific aims: 1) Determine the energetics of the bipartite USP-Ub interaction in USP1 and USP2 (a structural homolog of USP1). Assess the contribution of the bipartite interaction to ubiquitin recognition and catalysis by double mutation analysis; 2) Probe the specificity of USP1/UAF1 using a physiological substrate and its close mimics. A new AlphaScreen-based assay will be developed to improve both the throughput and sensitivity of the deubiquitylation assay; 3) Determine the molecular mechanism by which UAF1 upregulates the activity of USP1 and the closely related human USP46. We will characterize the USP1/UAF1 and USP46/UAF1 complexes and map the interaction sites between UAF1 and the two USPs. The molecular basis for the stimulation of the USP enzymatic activity by UAF1 will be interrogated by enzymological approaches. Taken together, these studies have the potential to uncover important insights into the specificity and regulation of the prevalent USP WD40-repeat protein complexes. Further, our study will suggest new directions for pharmacologic intervention of this important class of human USPs.

描述（由申请人提供）：人去泛素化酶（DUBs）的异常调节与许多人类疾病的发病机制有关，包括癌症、神经退行性疾病和病毒感染。泛素特异性蛋白酶（USPs）是五个已知DUB家族中最大的家族。人类USPs正在成为药理学干预的有希望的目标。然而，缺乏对USPs的特异性和调控的理解阻碍了开发新疗法的进展。值得注意的是，最近对人类dub的全球蛋白质组学分析显示，超过30个人类USPs与wd40重复蛋白特异性相关。鉴于其广泛存在，WD40-重复蛋白与USP之间的相互作用可能是调节USP活性的重要途径。本应用程序的重点是一个原型的USP wd40重复蛋白复合物，人类USP1/UAF1，及其密切的同源物。本申请的总体目标是深入了解人类USP和USP WD40-repeat蛋白复合物的特异性和调控。有三个具体目的：1)确定USP1和USP2 （USP1的结构同源物）中USP-Ub相互作用的能量学。通过双突变分析评估两部分相互作用对泛素识别和催化的贡献；2)利用生理底物及其相近的模拟物探测USP1/UAF1的特异性。将开发一种新的基于alphascreen的检测方法，以提高去泛素化检测的通量和灵敏度；3)确定UAF1上调USP1及与之密切相关的人类USP46活性的分子机制。我们将描述USP1/UAF1和USP46/UAF1复合物，并绘制UAF1与两个USPs之间的相互作用位点。UAF1刺激USP酶活性的分子基础将通过酶学方法进行探讨。综上所述，这些研究有可能揭示普遍的USP WD40-repeat蛋白复合物的特异性和调控的重要见解。此外，我们的研究将为这类重要的人类USPs的药物干预提供新的方向。