Levy-Mintz P, Kielian M
Department of Cell Biology, Albert Einstein College of Medicine, Bronx, New York 10461.
J Virol. 1991 Aug;65(8):4292-300. doi: 10.1128/JVI.65.8.4292-4300.1991.
Semliki Forest virus (SFV), an alphavirus, infects cells via a low pH-triggered membrane fusion reaction that takes place within the cellular endocytic pathway. Fusion is mediated by the heterotrimeric virus spike protein, which undergoes conformational changes upon exposure to low pH. The SFV E1 spike subunit contains a hydrophobic domain of 23 amino acids that is highly conserved among alphaviruses. This region is also homologous to a domain of the rotavirus outer capsid protein VP4. Mutagenesis of an SFV spike protein cDNA was used to evaluate the role of the E1 domain in membrane fusion. Mutant spike proteins were expressed in COS cells and assayed for cell-cell fusion activity. Four mutant phenotypes were identified: (i) substitution of Gln for Lys-79 or Leu for Met-88 had no effect on spike protein fusion activity; (ii) substitution of Ala for Asp-75, Ala for Gly-83, or Ala for Gly-91 shifted the pH threshold of fusion to a more acidic range; (iii) mutation of Pro-86 to Asp, Gly-91 to Pro, or deletion of amino acids 83 to 92 resulted in retention of the E1 subunit within the endoplasmic reticulum; and (iv) substitution of Asp for Gly-91 completely blocked cell-cell fusion activity without affecting spike protein assembly or transport. These results argue that the conserved hydrophobic domain of SFV E1 is closely involved in membrane fusion and suggest that the homologous region in rotavirus VP4 may be involved in the entry pathway of this nonenveloped virus.
辛德毕斯病毒(SFV)是一种甲病毒,它通过在细胞内吞途径中发生的低pH值触发的膜融合反应来感染细胞。融合由异源三聚体病毒刺突蛋白介导,该蛋白在暴露于低pH值时会发生构象变化。SFV E1刺突亚基包含一个由23个氨基酸组成的疏水区,在甲病毒中高度保守。该区域也与轮状病毒外衣壳蛋白VP4的一个结构域同源。利用SFV刺突蛋白cDNA的诱变来评估E1结构域在膜融合中的作用。突变的刺突蛋白在COS细胞中表达,并检测其细胞间融合活性。鉴定出四种突变表型:(i)将Lys-79替换为Gln或将Met-88替换为Leu对刺突蛋白融合活性没有影响;(ii)将Asp-75替换为Ala、将Gly-83替换为Ala或将Gly-91替换为Ala会使融合的pH阈值向更酸性范围移动;(iii)将Pro-86突变为Asp、将Gly-91突变为Pro或缺失氨基酸83至92导致E1亚基保留在内质网中;(iv)将Gly-91替换为Asp完全阻断细胞间融合活性,而不影响刺突蛋白的组装或运输。这些结果表明,SFV E1保守的疏水区与膜融合密切相关,并表明轮状病毒VP4中的同源区域可能参与这种无包膜病毒的进入途径。