Molecular determinants of adenovirus serotype 5 fibre binding to its cellular receptor CAR

被引:63
作者
Santis, G
Legrand, V
Hong, SS
Davison, E
Kirby, I
Imler, JL
Finberg, RW
Bergelson, JM
Mehtali, M
Boulanger, P
机构
[1] Guys Hosp, Dept Resp Med & Allergy, London SE1 9RT, England
[2] Transgene SA, Dept Gene Therapy, F-67000 Strasbourg, France
[3] Fac Med Montpellier, Inst Biol, CNRS UMR 5812, Lab Virol & Pathogenese Mol, F-34060 Montpellier, France
[4] Harvard Univ, Sch Med, Dana Farber Canc Inst, Div Infect Dis, Boston, MA 02115 USA
[5] Childrens Hosp Philadelphia, Div Infect Dis & Immunol, Philadelphia, PA 19104 USA
基金
英国惠康基金;
关键词
D O I
10.1099/0022-1317-80-6-1519
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
Adenovirus (Ad) tropism is mediated in part through the fibre protein. The common coxsackie B virus and Ad receptor (CAR) was recently identified as the major receptor for subgroup C Ad serotype 5 (Ad5) and serotype 2 (Ad2) fibres, Effects of mutations in the Ad5 fibre gene were studied to assess domains of the fibre capsomer that could alter virus tropism without altering virus assembly and replication. All mutants that accumulated as fibre monomers failed to assemble with a penton base and proved lethal for Ad5 which suggests that the absence of infectious virions resulted in part from a defect in fibre penton base assembly. Cell binding capacity of all fibre mutants was investigated in cell binding competition experiments with adenovirions using CHO-CAR cells (CHO cells that have been transfected with CAR cDNA and express functional CAR). The results suggest that the R-sheet of the Ad5 fibre knob monomer contains binding motifs for CAR and that beta-strands E and F, or a region close to them, may also be involved in receptor recognition.
引用
收藏
页码:1519 / 1527
页数:9
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