Golabek A A, Kida E, Walus M, Perez C, Wisniewski T, Soto C
Department of Pathological Neurobiology, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, New York 10314 USA.
Biophys J. 2000 Aug;79(2):1008-15. doi: 10.1016/S0006-3495(00)76354-5.
Immunocytochemical, biochemical, and molecular genetic studies indicate that apolipoprotein E (apoE) plays an important role in the process of amyloidogenesis-beta. However, there is still no clear translation of these data into the pathogenesis of amyloidosis-beta. Previous studies demonstrated sodium dodecyl sulfate (SDS)-resistant binding of apoE to the main component of Alzheimer's amyloid-A beta and modulation of A beta aggregation by apoE in vitro. To more closely characterize apoE-A beta interactions, we have studied the binding of thrombolytic fragments of apoE3 to A beta in vitro by using SDS-polyacrylamide gel electrophoresis and intrinsic fluorescence quenching. Here we demonstrate that SDS-resistant binding of A beta is mediated by the receptor-binding, N-terminal domain of apoE3. Under native conditions, both the N- and C-terminal domains of apoE3 bind A beta; however, the former does so with higher affinity. We propose that the modulation of A beta binding to the N-terminal domain of apoE is a potential therapeutic target for the treatment of amyloidosis-beta.
免疫细胞化学、生物化学和分子遗传学研究表明,载脂蛋白E(apoE)在β淀粉样蛋白生成过程中起重要作用。然而,这些数据仍未明确转化为β淀粉样变性的发病机制。先前的研究表明,apoE与阿尔茨海默病淀粉样蛋白 - Aβ的主要成分存在抗十二烷基硫酸钠(SDS)的结合,且在体外apoE可调节Aβ聚集。为更深入地描述apoE - Aβ相互作用,我们利用SDS - 聚丙烯酰胺凝胶电泳和内在荧光猝灭技术,在体外研究了apoE3的溶栓片段与Aβ的结合。在此我们证明,Aβ的抗SDS结合是由apoE3的受体结合N末端结构域介导的。在天然条件下,apoE3的N末端和C末端结构域均能结合Aβ;然而,前者的亲和力更高。我们提出,调节Aβ与apoE N末端结构域的结合是治疗β淀粉样变性的一个潜在治疗靶点。