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Surface protein complexes of oral treponemes: assembly and host cell interactions

口腔密螺旋体的表面蛋白复合物：组装和宿主细胞相互作用

基本信息

批准号：
7826782
负责人：
J CHRISTOPHER FENNO
金额：
$ 38.63万
依托单位：
UNIVERSITY OF MICHIGAN AT ANN ARBOR
依托单位国家：
美国
项目类别：
财政年份：
2009
资助国家：
美国
起止时间：
2009-05-05 至 2012-04-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7826782
关键词：
Affect Anabolism Animal Model Bacteria Bacterial Proteins Behavior Binding Biochemical Cell Communication Cell Surface Receptors Cells Cellular Assay Chronic Complex Environment Enzymes Epithelial Cells Epithelial Receptor Cell Event Extracellular Matrix Genetic Gingiva Goals Human Individual Infection Inflammatory Knowledge Laboratories Lead Lesion Lipoproteins Mediating Mediator of activation protein Membrane Membrane Proteins Microbe Molecular Analysis Molecular Biology Mutation Nutrient Operon Oral Order Spirochaetales Organism Penetration Peptide Hydrolases Periodontal Diseases Permeability Positioning Attribute Process Protein Binding Proteins Proteolytic Processing Public Health Qualifying Refractory Reporting Research Role Series Surface TLR2 gene Testing Tissues Treponema denticola acquired immunity cytotoxic dentilisin genetic analysis insight interest member oral spirochetes polypeptide protein complex receptor response

项目摘要

DESCRIPTION (provided by applicant): The goal of this research is to characterize expression and assembly of Treponema denticola (Td) surface proteins that mediate interactions with host tissue, thereby gaining insight into mechanisms of periodontal disease. We focus on analysis of two Td protein complexes that directly affect host cells: the oligomeric Msp protein and the PrtP lipoprotein protease complex. The overall hypothesis is that Msp and PrtP are major contributors to Td cytopathic behavior in periodontal disease. Expression of Msp and the PrtP complex are interdependent. To understand their roles in microbe-host interactions, we must understand how these molecules are expressed and interact in the spirochete. We propose genetic analysis of structural features and interactions of these complexes and their components. Our approach is to define the mechanisms of interdependence between Msp and the PrtP complex in order to characterize their roles in microbe-host interactions. Aim 1: Determine requirements for assembly and activity of the PrtP complex. We will construct a series of specific mutations in the protease locus that will enable us to characterize posttranslational processing of PrcA and PrtP, expression of PrcB, localization of protease complex proteins and assembly of the active protease complex. Aim 2: Determine the role of Msp in biosynthesis of protease complex proteins, and the role of the protease in oligomerization of Msp. We will characterize interactions between Msp and protease operon proteins that influence expression and activity of each outer membrane complex. Aim 3: Characterize interactions of Td outer membrane components with epithelial cells. To further studies of host cell responses to Td challenge, we will characterize interactions between Msp and a putative receptor identified on epithelial cells and characterize early events in epithelial cell innate responses to the PrtP protease complex and Msp, with the goal of differentiating between roles of Msp and the protease complex in cellular responses to Td. This project, involving genetic and biochemical analyses of Td outer membrane complex expression and analysis of Td effects on host cells, will contribute to molecular analysis of microbe-host interactions in the oral environment. Our laboratory is uniquely positioned to conduct these studies. Completion of these Aims will contribute to both basic knowledge of spirochete molecular biology and to understanding of microbe-host interactions in chronic infections such as periodontal diseases. Public Health Significance: This project will provide information on how a key bacterium involved in initiation periodontal disease interacts with human cells. The studies will first characterize the process of protein complex assembly on the bacterial surface. Then we will determine which specific proteins on human cells these complexes bind to, and then assay cellular responses to bacterial protein complexes binding to cell surface receptors.

描述（由申请人提供）：本研究的目的是表征密螺旋体（Td）表面蛋白的表达和组装，这些蛋白介导与宿主组织的相互作用，从而深入了解牙周病的机制。我们重点分析了直接影响宿主细胞的两种Td蛋白复合物：低聚物Msp蛋白和PrtP脂蛋白蛋白酶复合物。总的假设是Msp和PrtP是牙周病中Td细胞病变行为的主要贡献者。Msp和PrtP复合物的表达是相互依赖的。为了了解它们在微生物-宿主相互作用中的作用，我们必须了解这些分子是如何在螺旋体中表达和相互作用的。我们建议对这些复合物及其组分的结构特征和相互作用进行遗传分析。我们的方法是定义Msp和PrtP复合物之间相互依赖的机制，以表征它们在微生物-宿主相互作用中的作用。目标1：确定PrtP复合物的组装和活性要求。我们将在蛋白酶位点构建一系列特异性突变，这将使我们能够表征PrcA和PrtP的翻译后加工、PrcB的表达、蛋白酶复合物蛋白的定位和活性蛋白酶复合物的组装。目的2：确定Msp在蛋白酶复合物蛋白的生物合成中的作用，以及蛋白酶在Msp寡聚化中的作用。我们将描述影响每个外膜复合物表达和活性的Msp和蛋白酶操纵子蛋白之间的相互作用。目的3：表征Td外膜组分与上皮细胞的相互作用。为了进一步研究宿主细胞对Td的反应，我们将描述Msp与上皮细胞上一种假定的受体之间的相互作用，并描述上皮细胞对PrtP蛋白酶复合物和Msp先天反应的早期事件，目的是区分Msp和蛋白酶复合物在细胞对Td反应中的作用。本项目将对口腔环境中微生物与宿主相互作用的分子分析进行深入的研究，包括Td外膜复合物表达的遗传和生化分析以及Td对宿主细胞的作用分析。我们的实验室在进行这些研究方面具有独特的优势。这些目标的完成将有助于螺旋体分子生物学的基本知识和对慢性感染（如牙周病）中微生物-宿主相互作用的理解。公共卫生意义：该项目将提供有关牙周病起始期的关键细菌如何与人类细胞相互作用的信息。这些研究将首先描述蛋白质复合物在细菌表面组装的过程。然后，我们将确定这些复合物与人类细胞上的哪些特定蛋白质结合，然后分析细胞对细菌蛋白复合物与细胞表面受体结合的反应。