Rong L, Gendron K, Strohl B, Shenoy R, Wool-Lewis R J, Bates P
Department of Microbiology, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
J Virol. 1998 Jun;72(6):4552-9. doi: 10.1128/JVI.72.6.4552-4559.1998.
Tva is the cellular receptor for subgroup A avian leukosis and sarcoma virus (ALSV-A). The viral interaction domain of Tva is determined by a 40-residue, cysteine-rich module closely related to the ligand binding domain of the human low-density lipoprotein receptor (LDLR). In this report, we examined the role of the LDLR-like module of Tva in envelope binding and viral infection by mutational analysis. We found that the entire LDLR module in Tva is essential for efficient binding to the viral envelope protein. However, the 17 N-terminal residues of this module can be deleted without affecting receptor function, suggesting that the major determinants for viral entry are located at the C terminus of the module. The effect on viral infection of many amino acid substitutions and deletions in the LDLR module is context dependent, suggesting that the residues important for viral entry are dispersed throughout the LDLR module. In addition, we found that all 27 mutations at residues D46, E47, and W48 greatly reduced envelope binding. These results are discussed in relation to a recently elucidated structure for an LDLR module.
Tva是A亚群禽白血病和肉瘤病毒(ALSV-A)的细胞受体。Tva的病毒相互作用结构域由一个40个氨基酸残基的富含半胱氨酸的模块决定,该模块与人低密度脂蛋白受体(LDLR)的配体结合结构域密切相关。在本报告中,我们通过突变分析研究了Tva的LDLR样模块在包膜结合和病毒感染中的作用。我们发现,Tva中的整个LDLR模块对于有效结合病毒包膜蛋白至关重要。然而,该模块的17个N端残基可以删除而不影响受体功能,这表明病毒进入的主要决定因素位于该模块的C端。LDLR模块中许多氨基酸取代和缺失对病毒感染的影响取决于上下文,这表明对病毒进入重要的残基分散在整个LDLR模块中。此外,我们发现D46、E47和W48残基处的所有27个突变都大大降低了包膜结合。结合最近阐明的LDLR模块结构对这些结果进行了讨论。