The cellular receptor to human rhinovirus 2 binds around the 5-fold axis and not in the canyon: a structural view

被引:104
作者
Hewat, EA
Neumann, E
Conway, JF
Moser, R
Ronacher, B
Marlovits, TC
Blaas, D
机构
[1] Inst Biol Struct Jean Pierre Ebel, F-38027 Grenoble, France
[2] Univ Vienna, Inst Biochem, Vienna Bioctr VBC, A-1030 Vienna, Austria
关键词
cellular receptor; cryo-electron microscopy; HRV2; image analysis; VLDL-R;
D O I
10.1093/emboj/19.23.6317
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
Human rhinovirus serotype 2 (HRV2) belongs to the minor group of HRVs that bind to members of the LDL-receptor family including the very low density lipoprotein (VLDL)-receptor (VLDL-R). We have determined the structures of the complex between HRV2 and soluble fragments of the VLDL-R to 15 Angstrom resolution by cryo-electron microscopy. The receptor fragments, which include the first three ligand-binding repeats of the VLDL-R (V1-3), bind to the small star-shaped dome on the icosahedral 5-fold axis. This is in sharp contrast to the major group of HRVs where the receptor site for ICAM-1 is located at the base of a depression around each 5-fold axis. Homology models of the three domains of V1-3 were used to explore the virus-receptor interaction. The footprint of VLDL-R on the viral surface covers the BC- and HI-loops on VP1.
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页码:6317 / 6325
页数:9
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