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Characterization of the Role of ARH on LDLR Function

ARH 对 LDLR 功能作用的表征

基本信息

批准号：
7820963
负责人：
Peter A. Michaely
金额：
$ 1.26万
依托单位：
UT SOUTHWESTERN MEDICAL CENTER
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：
2009-06-01 至 2010-10-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7820963
关键词：
Adaptor Signaling Protein Address Animals Applications Grants Atherosclerosis Back Binding Biochemical Biochemistry Biological Assay Blood Circulation Cell surface Cells Cholesterol Clathrin Complex Cytoplasmic Tail Data Docking Electron Microscopy Endosomes Ensure Fibroblasts Goals Lipoprotein Binding Lipoproteins Low Density Lipoprotein Receptor Low-Density Lipoproteins Lymphocyte Mediating Microscopy Molecular Molecular Conformation Pathway interactions Play Process Proteins Recycling Research Research Design Research Personnel Role Serum Site Staging Surface System Testing Triglycerides Vascular Diseases Very low density lipoprotein Zebrafish coated pit hypercholesterolemia in vivo insight interdisciplinary approach link protein man novel prevent receptor function receptor mediated endocytosis receptor recycling research study tool trafficking uptake

项目摘要

DESCRIPTION (provided by applicant): The clearance of low density lipoprotein (LDL) and very low density lipoprotein (VLDL) by LDL receptor (LDLR) mediated endocytosis plays a critical role in preventing atherosclerosis and vascular disease. The recent finding that the adaptor protein, ARH, binds to the FDNPVY sequence on the LDLR and is required for LDL clearance has provided a tool with which to characterize the molecular mechanisms by which the LDLR mediates lipoprotein uptake and clearance. Recent studies and our preliminary data indicate that ARH plays a complex role in LDLR function. Our hypothesis is that ARH is principally involved in the uptake of LDL and that ARH functions at three levels in the uptake process: first, ARH promotes the ability of the LDLR to bind LDL; second, ARH promotes the uptake of LDLR-LDL complexes; and third, ARH ensures efficient release of LDL from the LDLR in endosomes. This grant proposal will employ a multidisciplinary approach using biochemistry, microscopy and animal studies to identify the mechanisms by which ARH promotes the binding, uptake and degradation of lipoproteins. Experiments will identify the regions of ARH that are responsible for promoting LDL binding, characterize the role of ARH in LDL and VLDL uptake, and determine the function of ARH in the endosomal trafficking of LDL and the LDLR. We will also examine the role of novel ARH binding partners in LDLR function. ARH is a multifunctional adaptor protein and different subsets of binding partners may participate at different stages in the lipoprotein binding and uptake pathway. The characterization of the function of ARH and its associated proteins in lipoprotein uptake by LDLR may clarify our understanding of the clearance process.

描述（由申请人提供）：通过LDL受体（LDLR）介导的内吞作用清除低密度脂蛋白（LDL）和极低密度脂蛋白（VLDL）在预防动脉粥样硬化和血管疾病中起关键作用。最近发现，衔接蛋白ARH结合LDLR上的FDNPVY序列，并且是LDL清除所需的，这为表征LDLR介导脂蛋白摄取和清除的分子机制提供了一种工具。最近的研究和我们的初步数据表明，ARH在LDLR功能中起着复杂的作用。我们的假设是ARH主要参与LDL的摄取，并且ARH在摄取过程中在三个水平起作用：首先，ARH促进LDLR结合LDL的能力;第二，ARH促进LDLR-LDL复合物的摄取;第三，ARH确保LDL从内体中的LDLR有效释放。这项拨款提案将采用生物化学，显微镜和动物研究的多学科方法，以确定ARH促进脂蛋白结合，吸收和降解的机制。实验将确定负责促进LDL结合的ARH区域，表征ARH在LDL和VLDL摄取中的作用，并确定ARH在LDL和LDLR的内体运输中的功能。我们还将研究新型ARH结合伴侣在LDLR功能中的作用。ARH是一种多功能的衔接蛋白，不同的结合伴侣亚群可能参与脂蛋白结合和摄取途径的不同阶段。ARH及其相关蛋白在LDLR摄取脂蛋白中的功能的表征可以澄清我们对清除过程的理解。