Netter Robert C, Amberg Sean M, Balliet John W, Biscone Mark J, Vermeulen Arwen, Earp Laurie J, White Judith M, Bates Paul
Department of Microbiology, University of Pennsylvania School of Medicine, 225 Johnson Pavilion, 3610 Hamilton Walk, Philadelphia, PA 19104-6076, USA.
J Virol. 2004 Dec;78(24):13430-9. doi: 10.1128/JVI.78.24.13430-13439.2004.
Fusion proteins of enveloped viruses categorized as class I are typified by two distinct heptad repeat domains within the transmembrane subunit. These repeats are important structural elements that assemble into the six-helix bundles characteristic of the fusion-activated envelope trimer. Peptides derived from these domains can be potent and specific inhibitors of membrane fusion and virus infection. To facilitate our understanding of retroviral entry, peptides corresponding to the two heptad repeat domains of the avian sarcoma and leukosis virus subgroup A (ASLV-A) TM subunit of the envelope protein were characterized. Two peptides corresponding to the C-terminal heptad repeat (HR2), offset from one another by three residues, were effective inhibitors of infection, while two overlapping peptides derived from the N-terminal heptad repeat (HR1) were not. Analysis of envelope mutants containing substitutions within the HR1 domain revealed that a single amino acid change, L62A, significantly reduced sensitivity to peptide inhibition. Virus bound to cells at 4 degrees C became sensitive to peptide within the first 5 min of elevating the temperature to 37 degrees C and lost sensitivity to peptide after 15 to 30 min, consistent with a transient intermediate in which the peptide binding site is exposed. In cell-cell fusion experiments, peptide inhibitor sensitivity occurred prior to a fusion-enhancing low-pH pulse. Soluble receptor for ASLV-A induces a lipophilic character in the envelope which can be measured by stable liposome binding, and this activation was found to be unaffected by inhibitory HR2 peptide. Finally, receptor-triggered conformational changes in the TM subunit were also found to be unaffected by inhibitory peptide. These changes are marked by a dramatic shift in mobility on sodium dodecyl sulfate-polyacrylamide gel electrophoresis, from a subunit of 37 kDa to a complex of about 80 kDa. Biotinylated HR2 peptide bound specifically to the 80-kDa complex, demonstrating a surprisingly stable envelope conformation in which the HR2 binding site is exposed. These experiments support a model in which receptor interaction promotes formation of an envelope conformation in which the TM subunit is stably associated with its target membrane and is able to bind a C-terminal peptide.
被归类为I类的包膜病毒融合蛋白的典型特征是跨膜亚基内有两个不同的七肽重复结构域。这些重复序列是重要的结构元件,可组装成融合激活的包膜三聚体特有的六螺旋束。源自这些结构域的肽可以是膜融合和病毒感染的有效且特异性抑制剂。为了促进我们对逆转录病毒进入的理解,对与禽肉瘤和白血病病毒A亚群(ASLV-A)包膜蛋白的跨膜亚基的两个七肽重复结构域相对应的肽进行了表征。对应于C端七肽重复序列(HR2)的两个肽,彼此相差三个残基,是有效的感染抑制剂,而源自N端七肽重复序列(HR1)的两个重叠肽则不是。对HR1结构域内含有取代的包膜突变体的分析表明,单个氨基酸变化L62A显著降低了对肽抑制的敏感性。在4℃下与细胞结合的病毒在温度升高到37℃的前5分钟内对肽变得敏感,并在15至30分钟后对肽失去敏感性,这与肽结合位点暴露的瞬时中间体一致。在细胞-细胞融合实验中,肽抑制剂敏感性在融合增强的低pH脉冲之前出现。ASLV-A的可溶性受体在包膜中诱导出一种亲脂特性,这可以通过稳定的脂质体结合来测量,并且发现这种激活不受抑制性HR2肽的影响。最后,还发现受体触发的跨膜亚基构象变化不受抑制性肽的影响。这些变化的特征是在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳上迁移率发生显著变化,从37 kDa的亚基变为约80 kDa的复合物。生物素化的HR2肽特异性结合到80 kDa的复合物上,表明存在一种令人惊讶的稳定包膜构象,其中HR2结合位点暴露。这些实验支持了一个模型,即受体相互作用促进包膜构象的形成,其中跨膜亚基与其靶膜稳定结合并能够结合C端肽。