Hantavirus Gc glycoprotein: evidence for a class II fusion protein

被引:61
作者
Tischler, ND
Gonzalez, A
Perez-Acle, T
Rosemblatt, M
Valenzuela, PDT
机构
[1] Pontificia Univ Catolica Chile, Fdn Ciencias Vida, Ctr Genom & Bioinformat, Santiago, Chile
[2] Pontificia Univ Catolica Chile, Inst Milenio MIFAB, Ctr Genom & Bioinformat, Santiago, Chile
[3] Univ Andres Bello, Santiago, Chile
关键词
D O I
10.1099/vir.0.81083-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Hantavirus cell entry is promoted by its envelope glycoproteins, Gin and Gc, through cell attachment and by fusion between viral and endosomal membranes at low pH. However, the role of Gn and Gc in receptor binding and cell fusion has not yet been defined. In this work, a sequence presenting characteristics similar to those of class II fusion peptides (FPs) of alphavirus Ell and flavivirus E proteins is identified within the hantavirus Gc glycoprotein. A three-dimensional comparative molecular model based on crystallographic data of tick-borne encephalitis virus E protein is proposed for the Andes virus (ANDV) Gc ectodomain, which supports a feasible class II fusion-protein fold. In vitro experimental evidence is provided for the binding activity of the ANDV FP candidate to artificial membranes, as demonstrated by fluorescence anisotropy assays. Taken together, these results support the hypothesis that the Gc glycoprotein of hantaviruses and of other members of the family Bunyaviridae directs the viral fusion activity and that it may be classified as a class II viral fusion protein.
引用
收藏
页码:2937 / 2947
页数:11
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