Yao Q, Compans R W
Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
J Virol. 1995 Nov;69(11):7045-53. doi: 10.1128/JVI.69.11.7045-7053.1995.
We have investigated the roles of the cytoplasmic domains of the human parainfluenza virus type 2 (PI2) and type 3 (PI3) fusion (F) proteins in protein transport and cell fusion activity. By using the vaccinia virus-T7 transient expression system, a series of F protein cytoplasmic tail truncation mutants was studied with respect to intracellular and surface expression and the ability to induce cell fusion when coexpressed with the corresponding hemagglutinin-neuraminidase (HN) proteins. All of the cytoplasmic tail truncation mutants of PI2F were expressed at high levels intracellularly or on cell surfaces as measured by immunoprecipitation and cell surface biotinylation assays. In addition, when coexpressed with PI2HN, these truncation mutants of PI2F were all found to be essentially unimpaired in the ability to induce cell fusion as measured by a quantitative cell fusion assay. In contrast, surface expression and cell fusion activity were found to be eliminated by a mutant of PI3F in which the entire cytoplasmic tail was deleted, and the mutant protein appeared to be unable to assemble into a high-molecular-weight oligomeric structure. To further investigate whether there is a specific sequence requirement in the cytoplasmic tail of PI3F, a chimeric protein consisting of the PI3F extracellular and transmembrane domains and the PI2F cytoplasmic tail was constructed. This chimeric protein was detected on the surface, and it was capable of inducing cell fusion when expressed together with PI3HN, although the fusogenic activity was reduced compared with that of wild-type PI3F. These results demonstrate that although PI2 and PI3 viruses belong to the same parainfluenza virus genus, these viruses show marked differences with respect to functional requirements for the cytoplasmic tail of the F glycoprotein.
我们研究了人副流感病毒2型(PI2)和3型(PI3)融合(F)蛋白的胞质结构域在蛋白质运输和细胞融合活性中的作用。通过使用痘苗病毒-T7瞬时表达系统,研究了一系列F蛋白胞质尾截短突变体在细胞内和表面的表达情况,以及与相应的血凝素-神经氨酸酶(HN)蛋白共表达时诱导细胞融合的能力。通过免疫沉淀和细胞表面生物素化分析测定,PI2F的所有胞质尾截短突变体在细胞内或细胞表面均高水平表达。此外,通过定量细胞融合分析测定,当与PI2HN共表达时,这些PI2F截短突变体在诱导细胞融合的能力上基本未受损。相比之下,发现PI3F的一个缺失整个胞质尾的突变体消除了表面表达和细胞融合活性,并且该突变蛋白似乎无法组装成高分子量的寡聚结构。为了进一步研究PI3F胞质尾是否存在特定的序列要求,构建了一种由PI3F的胞外和跨膜结构域以及PI2F的胞质尾组成的嵌合蛋白。该嵌合蛋白在表面被检测到,并且当与PI3HN一起表达时能够诱导细胞融合,尽管其融合活性与野生型PI3F相比有所降低。这些结果表明,尽管PI2和PI3病毒属于同一副流感病毒属,但这些病毒在F糖蛋白胞质尾的功能要求方面存在显著差异。