He Wanxia, Shi Qi, Hu Xiangyou, Yan Riqiang
Department of Neurosciences, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
J Biol Chem. 2007 Oct 5;282(40):29144-51. doi: 10.1074/jbc.M704181200. Epub 2007 Aug 15.
Reticulon 3 (RTN3) has recently been shown to modulate Alzheimer BACE1 activity and to play a role in the formation of dystrophic neurites present in Alzheimer brains. Despite the functional importance of this protein in Alzheimer disease pathogenesis, the functional correlation to the structural domain of RTN3 remained unclear. RTN3 has two long transmembrane domains, but its membrane topology was not known. We report here that the first transmembrane domain dictates membrane integration and its membrane topology. RTN3 adopts a omega-shape structure with two ends facing the cytosolic side. Subtle changes in RTN3 membrane topology can disrupt its binding to BACE1 and its inhibitory effects on BACE1 activity. Thus, the determination of RTN3 membrane topology may provide an important structural basis for our understanding of its cellular functions.
最近研究表明,网织蛋白3(RTN3)可调节阿尔茨海默病β-分泌酶1(BACE1)的活性,并在阿尔茨海默病大脑中出现的营养不良性神经突的形成中发挥作用。尽管该蛋白在阿尔茨海默病发病机制中具有重要功能,但其与RTN3结构域的功能相关性仍不清楚。RTN3有两个长跨膜结构域,但其膜拓扑结构尚不清楚。我们在此报告,第一个跨膜结构域决定膜整合及其膜拓扑结构。RTN3采用ω形结构,两端面向胞质侧。RTN3膜拓扑结构的细微变化会破坏其与BACE1的结合及其对BACE1活性的抑制作用。因此,确定RTN3膜拓扑结构可能为我们理解其细胞功能提供重要的结构基础。