Luo Z, Weiss S R
Department of Microbiology, University of Pennsylvania School of Medicine, Philadelphia 19104-6076, USA.
Virology. 1998 May 10;244(2):483-94. doi: 10.1006/viro.1998.9121.
The spike (S) protein of coronavirus mouse hepatitis virus (MHV), mediates attachment and fusion during viral entry and cell-to-cell fusion later in infection. By analogy with other viral proteins that induce cell fusion the MHV S protein would be expected to have a hydrophobic stretch of amino acids that serves as a fusion peptide. Sequence analysis suggests that the S protein falls within the group of fusion proteins having internal rather than N-terminal fusion peptides. Based on the features of known viral fusion peptides, we identified two regions (PEP1 and PEP2) of MHV-A59 S2 as possible fusion peptides. Site-directed mutagenesis and an in viro cell-to-cell fusion assay were used to evaluate the roles of PEP1 and PEP2, as well as a third previously identified putative fusion domain (PEP3) in membrane fusion. Substitution of bulky hydrophobic residues with charged residues within PEP1 affects the fusion activity of the S protein without affecting processing and surface expression. Similar substitutions within PEP2 result in a fusion-negative phenotype; however, these mutant S proteins also exhibit defects in protein processing and surface expression which likely explain the loss of the ability to induce fusion. Thus PEP1 remains a candidate fusion peptide, while PEP2 may play a significant role in the overall structure or oligomerization of the S protein. PEP3 is an unlikely putative fusion peptide since it is not conserved among coronaviruses and nonconservative amino acid substitutions in PEP3 have minimal effects on cell-to-cell fusion.
冠状病毒小鼠肝炎病毒(MHV)的刺突(S)蛋白在病毒进入过程中介导附着和融合,并在感染后期介导细胞间融合。与其他诱导细胞融合的病毒蛋白类似,预计MHV S蛋白具有一段疏水性氨基酸序列作为融合肽。序列分析表明,S蛋白属于具有内部而非N端融合肽的融合蛋白组。基于已知病毒融合肽的特征,我们将MHV-A59 S2的两个区域(PEP1和PEP2)鉴定为可能的融合肽。采用定点诱变和体外细胞间融合试验来评估PEP1和PEP2以及先前鉴定的第三个假定融合结构域(PEP3)在膜融合中的作用。在PEP1内用带电荷残基取代大的疏水残基会影响S蛋白的融合活性,而不影响加工和表面表达。在PEP2内进行类似取代会导致融合阴性表型;然而,这些突变的S蛋白在蛋白质加工和表面表达方面也表现出缺陷,这可能解释了诱导融合能力的丧失。因此,PEP1仍然是一个候选融合肽,而PEP2可能在S蛋白的整体结构或寡聚化中发挥重要作用。PEP3不太可能是假定的融合肽,因为它在冠状病毒中不保守,并且PEP3中的非保守氨基酸取代对细胞间融合的影响最小。