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.
引用
收藏
页码:6317 / 6325
页数:9
相关论文
共 59 条
  • [51] Major and minor receptor group human rhinoviruses penetrate from endosomes by different mechanisms
    Schober, D
    Kronenberger, P
    Prchla, E
    Blaas, D
    Fuchs, R
    [J]. JOURNAL OF VIROLOGY, 1998, 72 (02) : 1354 - 1364
  • [52] RELATIONSHIP OF HUMAN RHINOVIRUS STRAIN-2 AND POLIOVIRUS AS INDICATED BY COMPARISON OF THE POLYMERASE GENE REGIONS
    SKERN, T
    SOMMERGRUBER, W
    BLAAS, D
    PIELER, C
    KUECHLER, E
    [J]. VIROLOGY, 1984, 136 (01) : 125 - 132
  • [53] Neutralizing antibody to human rhinovirus 14 penetrates the receptor-binding canyon
    Smith, TJ
    Chase, ES
    Schmidt, TJ
    Olson, NH
    Baker, TS
    [J]. NATURE, 1996, 383 (6598) : 350 - 354
  • [54] A CELL-ADHESION MOLECULE, ICAM-1, IS THE MAJOR SURFACE-RECEPTOR FOR RHINOVIRUSES
    STAUNTON, DE
    MERLUZZI, VJ
    ROTHLEIN, R
    BARTON, R
    MARLIN, SD
    SPRINGER, TA
    [J]. CELL, 1989, 56 (05) : 849 - 853
  • [55] CDNA CLONING REVEALS THAT THE MAJOR GROUP RHINOVIRUS RECEPTOR ON HELA-CELLS IS INTERCELLULAR-ADHESION MOLECULE-1
    TOMASSINI, JE
    GRAHAM, D
    DEWITT, CM
    LINEBERGER, DW
    RODKEY, JA
    COLONNO, RJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (13) : 4907 - 4911
  • [56] STRUCTURE OF THE MAJOR ANTIGENIC LOOP OF FOOT-AND-MOUTH-DISEASE VIRUS COMPLEXED WITH A NEUTRALIZING ANTIBODY - DIRECT INVOLVEMENT OF THE ARG-GLY-ASP MOTIF IN THE INTERACTION
    VERDAGUER, N
    MATEU, MG
    ANDREU, D
    GIRALT, E
    DOMINGO, E
    FITA, I
    [J]. EMBO JOURNAL, 1995, 14 (08) : 1690 - 1696
  • [57] Structure of human rhinovirus serotype 2 (HRV2)
    Verdaguer, N
    Blaas, D
    Fita, I
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2000, 300 (05) : 1179 - 1194
  • [58] Distinct cellular receptor interactions in poliovirus and rhinoviruses
    Xing, L
    Tjarnlund, K
    Lindqvist, B
    Kaplan, GG
    Feigelstock, D
    Cheng, RH
    Casasnovas, JM
    [J]. EMBO JOURNAL, 2000, 19 (06) : 1207 - 1216
  • [59] Sialylation of the host receptor may modulate entry of demyelinating persistent Theiler's virus
    Zhou, L
    Luo, Y
    Wu, Y
    Tsao, J
    Luo, M
    [J]. JOURNAL OF VIROLOGY, 2000, 74 (03) : 1477 - 1485