Low pH and Anionic Lipid-dependent Fusion of Uukuniemi Phlebovirus to Liposomes

被引:34
作者
Bitto, David [1 ]
Halldorsson, Steinar [1 ]
Caputo, Alessandro [1 ,2 ]
Huiskonen, Juha T. [1 ]
机构
[1] Univ Oxford, Wellcome Trust Ctr Human Genet, Div Struct Biol, Roosevelt Dr, Oxford OX3 7BN, England
[2] Univ Oxford, Dept Biochem, S Parks Rd, Oxford OX1 3QU, England
基金
英国惠康基金;
关键词
electron tomography; membrane; membrane fusion; virus entry; virus structure; bis(monoacylglycero)phosphate; bunyavirus; phlebovirus; SEMLIKI-FOREST-VIRUS; BORNE ENCEPHALITIS-VIRUS; MEMBRANE-FUSION; ELECTRON CRYOTOMOGRAPHY; SPONTANEOUS CURVATURE; SINDBIS VIRUS; FEVER; CHOLESTEROL; GLYCOPROTEIN; PROTEIN;
D O I
10.1074/jbc.M115.691113
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many phleboviruses (family Bunyaviridae) are emerging as medically important viruses. These viruses enter target cells by endocytosis and low pH-dependent membrane fusion in late endosomes. However, the necessary and sufficient factors for fusion have not been fully characterized. We have studied the minimal fusion requirements of a prototypic phlebovirus, Uukuniemi virus, in an in vitro virus-liposome assay. We show that efficient lipid mixing between viral and liposome membranes requires close to physiological temperatures and phospholipids with negatively charged headgroups, such as the late endosomal phospholipid bis(monoacylglycero)phosphate. We further demonstrate that bis(monoacylglycero)phosphate increases Uukuniemi virus fusion beyond the lipid mixing stage. By using electron cryotomography of viral particles in the presence or absence of liposomes, we observed that the conformation of phlebovirus glycoprotein capsomers changes from the native conformation toward a more elongated conformation at a fusion permissive pH. Our results suggest a rationale for phlebovirus entry in late endosomes.
引用
收藏
页码:6412 / 6422
页数:11
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