Provitera Paxton, El-Maghrabi Raafat, Scarlata S
Department of Physiology and Biophysics, State University of New York at Stony Brook, Stony Brook, NY 11796-8661, USA.
Biophys Chem. 2006 Jan 1;119(1):23-32. doi: 10.1016/j.bpc.2005.08.008. Epub 2005 Sep 23.
During the viral life cycle, an HIV protein, Gag, assembles at the host membrane, specifically at lipid raft regions, at very high concentrations leading to viral particle budding. Gag is post-translationally modified with an N-terminal myristate group which is thought to target Gag to lipid rafts thus aiding in assembly. Here we have analyzed the membrane binding of myristoylated HIV-1 Gag and a non-myristoylated form of HIV-1 Gag to various membrane models. After assessing the extent of myristoylation by HPLC and radiometric assays, we compared membrane binding using fluorescence methods. We found that myristoylated Gag shows a greater than twofold increase in binding affinity to model rafts. A structural model to explain these results is presented.
在病毒生命周期中,一种HIV蛋白Gag会在宿主细胞膜上组装,特别是在脂筏区域,以非常高的浓度导致病毒粒子出芽。Gag在翻译后会被N端肉豆蔻酰基修饰,该基团被认为会将Gag靶向脂筏,从而有助于组装。在此,我们分析了肉豆蔻酰化的HIV-1 Gag和非肉豆蔻酰化形式的HIV-1 Gag与各种膜模型的膜结合情况。通过高效液相色谱法(HPLC)和放射性测定法评估肉豆蔻酰化程度后,我们使用荧光方法比较了膜结合情况。我们发现,肉豆蔻酰化的Gag与模型脂筏的结合亲和力增加了两倍多。本文提出了一个解释这些结果的结构模型。