Calreticulin's functions in the adaptive immune response

钙网蛋白在适应性免疫反应中的功能

• 批准号: 7213582
• 负责人: MALINI RAGHAVAN
• 金额: $ 29.85万
• 依托单位: UNIVERSITY OF MICHIGAN AT ANN ARBOR
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-03-15 至 2011-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7213582
• 关键词: Alanine; Antigen Presentation; Antigen Presentation Pathway; Antigen-Presenting Cells; Antigens; Apoptotic; Binding; Binding Sites; Biochemical; Calcium; Calnexin; Cell surface; Cells; Cellular Stress; Chickens; Class; Complex; Condition; Cross Presentation; Cross-Priming; Defect; Dimerization; Disulfides; Endoplasmic Reticulum; Endosomes; Glycoproteins; Heating; Histocompatibility Antigens Class I; IgY; Immune response; Immunity; Immunofluorescence Immunologic; In Vitro; Lectin; Link; Location; Major Histocompatibility Complex; Mass Spectrum Analysis; Mediating; Modeling; Molecular; Molecular Chaperones; Molecular Conformation; Mutate; Oligosaccharides; Pathway interactions; Peptides; Phagocytes; Physiological; Polysaccharides; Property; Proteins; Proteolysis; Quality Control; Role; Route; Site; Stress; Structure; Substrate Interaction; Surface; T-Lymphocyte; Tunicamycin; Vaccine Design; Virus Diseases; Work; activated protein C receptor; base; calreticulin; conformational conversion; dimer; in vivo; insight; mutant; polypeptide; protein folding; receptor; research study; trafficking; trans-Golgi Network; uptake

DESCRIPTION (provided by applicant): Calreticulin is an endoplasmic reticulum (ER) chaperone that promotes folding and assembly of glycoproteins, including major histocompatibility complex (MHC) class I molecules. Calreticulin also has the capacity to direct exogenous antigens onto the MHC class I antigen presentation pathway, a phenomenon called cross-presentation. As a lectin, Calreticulin interacts with monoglucosylated core glycans on glycoproteins. Under certain conditions, Calreticulin is able to bind polypeptide components of substrates. Calcium depletion and heat-treatment expose calreticulin's polypeptide binding site and enhance Calreticulin binding to polypeptide substrates in vitro and in vivo cells. These treatments also induce Calreticulin dimerization and oligomerization. The formation of Calreticulin dimers is additionally induced by other types of ER stress, including virus infection and tunicamycin treatment. It is our hypothesis that these conformational transitions and polypeptide-binding properties are important for calreticulin's protein folding and cross-priming functions in cells. The first specific aim explores the role of polypeptide binding by Calreticulin during MHC class I folding and assembly in cells. We propose partial proteolysis and mass spectrometry-based approaches to identify Calreticulin sub-domains that are mobilized by calcium depletion. Conserved hydrophobic residues of Calreticulin, that are predicted to be surface-exposed, will be mutated to alanines. Mutants that display defects in interactions with polypeptide components of MHC class I heavy chains in vitro, as well as other mutants with defects in binding oligosaccharide substrates, will be expressed in calreticulin-deficient cells, and assessed for the ability to facilitate MHC class I folding and assembly. Together, these studies will allow us to refine our working model for the calreticulin-substrate interaction cycle, in which alternating interactions with oligosaccharide and polypeptide components of substrates are proposed. We will attempt to crystallize truncated versions of Calreticulin that have enhanced ability to bind polypeptide substrates, and also crystallize Calreticulin complexes with chicken IgY fragments. The second specific aim will explore mechanisms of calreticulin-mediated cross-presentation. Intracellular trafficking of Calreticulin and calreticulin-associated peptides during cross-presentation will be assessed, to investigate the hypothesis of an endosome-trans Golgi network-ER trafficking route. The requirement for Calreticulin for cross-presentation of antigens associated with apoptotic cells will also be assessed. Finally, the effects of ER stress on Calreticulin trafficking, cell surface expression, and interactions with receptors on antigen presenting cells will be assessed. Understanding the molecular mechanisms of calreticulin's functions, and elucidation of conditions that enhance calreticulin's T cell priming activities, will facilitate more effective design of vaccines.

描述（由申请人提供）：钙网蛋白是一种内质网（ER）伴侣蛋白，促进糖蛋白的折叠和组装，包括主要组织相容性复合体（MHC） I类分子。钙网蛋白还具有引导外源抗原进入MHC I类抗原呈递途径的能力，这种现象被称为交叉呈递。钙网蛋白作为一种凝集素，与糖蛋白上的单糖基化核心聚糖相互作用。在一定条件下，钙网蛋白能够结合底物的多肽成分。在体外和体内细胞中，缺钙和热处理暴露了钙网蛋白的多肽结合位点，增强了钙网蛋白与多肽底物的结合。这些处理也诱导钙网蛋白二聚化和寡聚化。钙网蛋白二聚体的形成还可由其他类型的内质网应激诱导，包括病毒感染和tunicamycin治疗。我们的假设是，这些构象转变和多肽结合特性对钙调蛋白在细胞中的蛋白质折叠和交叉启动功能很重要。第一个具体目的是探讨钙网蛋白在MHC I类折叠和细胞组装过程中多肽结合的作用。我们提出基于部分蛋白水解和质谱的方法来鉴定钙网蛋白亚结构域，这些亚结构域是由钙耗尽动员的。钙网蛋白保守的疏水残基，预计是表面暴露的，将突变为丙氨酸。在体外与MHC I类重链多肽组分相互作用中显示缺陷的突变体，以及其他结合寡糖底物存在缺陷的突变体，将在钙调蛋白缺乏的细胞中表达，并评估其促进MHC I类折叠和组装的能力。总之，这些研究将使我们能够完善钙调蛋白-底物相互作用循环的工作模型，其中提出了与底物的低聚糖和多肽组分交替相互作用。我们将尝试结晶钙网蛋白的截断版本，它具有增强的结合多肽底物的能力，也结晶钙网蛋白与鸡IgY片段的复合物。第二个具体目标将探讨钙网蛋白介导的交叉呈递机制。将评估钙网蛋白和钙网蛋白相关肽在交叉呈现过程中的细胞内运输，以研究内核体-反高尔基网络-内质网运输路线的假设。钙网蛋白对凋亡细胞相关抗原交叉呈递的要求也将被评估。最后，我们将评估内质网应激对钙网蛋白运输、细胞表面表达以及与抗原提呈细胞受体相互作用的影响。了解钙调蛋白功能的分子机制，阐明钙调蛋白T细胞启动活性增强的条件，将有助于更有效地设计疫苗。