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低密度脂蛋白受体的结构与折叠

Low-density lipoprotein receptor structure and folding.

作者信息

Gent J, Braakman I

机构信息

Department of Bio-organic Chemistry 1, Utrecht University, Padualaan 8, 3584, CH Utrecht, The Netherlands.

出版信息

Cell Mol Life Sci. 2004 Oct;61(19-20):2461-70. doi: 10.1007/s00018-004-4090-3.

Abstract

The endoplasmic reticulum (ER) is a major cellular 'production factory' for many membrane and soluble proteins. A quality control system ensures that only correctly folded and assembled proteins leave the compartment. The low-density lipoprotein receptor (LDLR) is the prototype of a large family of structurally homologous cell surface receptors, which fold in the ER and function as endocytic and signaling receptors in a wide variety of cellular processes. Patients with familial hypercholesterolemia carry single or multiple mutations in their LDLR, which leads to malfunction of the protein, in most patients through misfolding of the receptor. As a result, clearance of cholesterol-rich LDL particles from the circulation decreases, and the elevated blood cholesterol levels cause early onset of atherosclerosis and an increased risk of cardiac disease in these patients. In this review, we will elaborate on the structural aspects of the LDLR and its folding pathway and compare it to other LDLR family members.

摘要

内质网(ER)是许多膜蛋白和可溶性蛋白的主要细胞“生产工厂”。质量控制系统确保只有正确折叠和组装的蛋白质才能离开该隔室。低密度脂蛋白受体(LDLR)是一大类结构同源细胞表面受体的原型,这些受体在ER中折叠,并在多种细胞过程中作为内吞和信号受体发挥作用。家族性高胆固醇血症患者的LDLR存在单个或多个突变,这会导致该蛋白功能异常,在大多数患者中是由于受体错误折叠所致。结果,循环中富含胆固醇的LDL颗粒的清除减少,血液胆固醇水平升高导致这些患者早期发生动脉粥样硬化并增加心脏病风险。在本综述中,我们将详细阐述LDLR的结构方面及其折叠途径,并将其与其他LDLR家族成员进行比较。

相似文献

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Low-density lipoprotein receptor structure and folding.低密度脂蛋白受体的结构与折叠
Cell Mol Life Sci. 2004 Oct;61(19-20):2461-70. doi: 10.1007/s00018-004-4090-3.

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