Friedland Natalia, Liou Heng-Ling, Lobel Peter, Stock Ann M
Center for Advanced Biotechnology and Medicine, Howard Hughes Medical Institute, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, 679 Hoes Lane, Piscataway, NJ 08854, USA.
Proc Natl Acad Sci U S A. 2003 Mar 4;100(5):2512-7. doi: 10.1073/pnas.0437840100. Epub 2003 Feb 18.
Niemann-Pick disease type C2 (NP-C2) is a fatal hereditary disease characterized by accumulation of low-density lipoprotein-derived cholesterol in lysosomes. Here we report the 1.7-A resolution crystal structure of the cholesterol-binding protein deficient in this disease, NPC2, and the characterization of its ligand binding properties. Human NPC2 binds the cholesterol analog dehydroergosterol with submicromolar affinity at both acidic and neutral pH. NPC2 has an Ig-like fold stabilized by three disulfide bonds. The structure of the bovine protein reveals a loosely packed region penetrating from the surface into the hydrophobic core that forms adjacent small cavities with a total volume of approximately 160 A(3). We propose that this region represents the incipient cholesterol-binding site that dilates to accommodate an approximately 740-A(3) cholesterol molecule.
尼曼-皮克C2型病(NP-C2)是一种致命的遗传性疾病,其特征是溶酶体中低密度脂蛋白衍生的胆固醇积累。在此,我们报告了这种疾病中缺乏的胆固醇结合蛋白NPC2的1.7埃分辨率晶体结构及其配体结合特性的表征。人NPC2在酸性和中性pH下均以亚微摩尔亲和力结合胆固醇类似物脱氢麦角固醇。NPC2具有由三个二硫键稳定的免疫球蛋白样折叠。牛蛋白的结构揭示了一个从表面穿透到疏水核心的松散堆积区域,该区域形成相邻的小腔,总体积约为160 ų。我们提出,该区域代表初始胆固醇结合位点,其会扩张以容纳一个约740 ų的胆固醇分子。