权益分类	功能权益	普通用户	{{item.name}}会员
{{category.name}}	{{benefitItem.name}}

A Proteomic Analysis of the AHR signaling Network

AHR 信号网络的蛋白质组学分析

基本信息

批准号：
7599127
负责人：
JOHN J LAPRES
金额：
$ 24.87万
依托单位：
MICHIGAN STATE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
资助国家：
美国
起止时间：
至
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/7599127
关键词：
ARA9 protein Address Affinity Chromatography Agonist Arts Aryl Hydrocarbon Receptor Biological Assay Biological Process Biology CDKN1A gene Cells Complex Computer Simulation Cytosol Data Dioxins Event Exposure to Gene Transfer Genes Goals Heat-Shock Proteins 90 Immune Immunophilins In Vitro Ligands Literature Liver Location Maps Mass Spectrum Analysis Mediating Modeling Molecular Chaperones Molecular Conformation Nature Peptidylprolyl Isomerase Play Poison Positioning Attribute Protein Analysis Protein Overexpression Proteins Proteomics Publishing RNA Interference Receptor Signaling Recruitment Activity Registries Reporting Risk Assessment Role Series Signal Transduction Site Small Interfering RNA System Testing Tetrachlorodibenzodioxin Time Tissues Toxic effect Transfection Viral Vector Western Blotting aryl hydrocarbon receptor ligand dimer in vitro Assay knock-down man member oncoprotein p21 receptor receptor binding research study retroviral-mediated superfund site tool

项目摘要

Aryl hydrocarbon receptor (AHR) agonists, such as 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), are some of the most toxic chemicals known to man. They also hold 4 of the top 10 positions within the EPA-ATSDR registry of priority substances that contaminate National Priority List. The toxicity of these compounds is primarily dependent upon the presence of a functional AHR signaling complex. This complex, in the absence of ligand consists of the AHR bound to a dimer of the heat shock protein of 90 kDa (Hsp90), the immunophilin-like protein, ARA9 (also known as XAP2 and AIP) and possibly several other factors (eg pp60src, p21). The role these chaperones play and their mechanism of action remains largely unknown. Our recent preliminary experiments suggest that ARA9 may function by recruiting other cellular factors to the AHR cytosolic complex. The role these cellular factors and other signaling systems play in the formation and integrity of the AHR cytosolic complex (upstream events) and how these other complex proteins influence AHR mediated toxicity (downstream events) has not been thoroughly explored. These signals may play important roles in the tissue specific biology and toxicity of AHR agonists. Our preliminary data and recent literature have led us to hypothesize: Secondary signaling, both upstream and downstream, plays an important role in AHR mediated signaling and toxicity through direct influence of the activity of the AHR cytosolic complex and perturbations of downstream signaling cascades. To address the hypothesis this project will look at the effects of secondary signaling on AHR biology in four specific aims (SA). SA1) Identify and characterize the proteins capable of interacting with the AHR in liver and immune cells in the absence and presence of ligand using tandem affinity purification, mass spectrometry and retroviral mediated gene transfer. SA2) Determine the fate of AHR complex members following ligand exposure using mass spectrometry and retroviral mediated gene transfer. SA3) Characterize the role of AHR-interacting proteins in ligand-induced signaling using RNAi, transient transfections and functional assays. SA4) Create a functional interaction network map for the AHR using proteins identified in the first aims and published reports and determine its overlap with regulatory networks. The completion of these aims will create a detailed picture of the AHR protein interaction network (AHR-PIN) and directly relate the proteins in this PIN to functional consequences for AHR mediated toxicity. Finally, the computational model that will be developed will generate new mechanistic directions for understanding the toxicity of AHR ligands and allow more accurate risk assessment for Superfund sites.

芳烃受体（AHR）激动剂，如2,3,7,8-四氯二苯并-对二恶英（TCDD），是其中的一些