 |
PDBsum entry 5ffl
|
|
|
|
 |
|
|
|
|
|
|
|
|
|
|
|
|
|
 |
|
|
|
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
|
|
|
|
|
|
|
|
|
|
Immune system
|
PDB id
|
|
|
|
5ffl
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
References listed in PDB file
|
 |
|
Key reference
|
 |
|
Title
|
 |
Discovery of a proteinaceous cellular receptor for a norovirus.
|
 |
|
Authors
|
 |
R.C.Orchard,
C.B.Wilen,
J.G.Doench,
M.T.Baldridge,
B.T.Mccune,
Y.C.Lee,
S.Lee,
S.M.Pruett-Miller,
C.A.Nelson,
D.H.Fremont,
H.W.Virgin.
|
 |
|
Ref.
|
 |
Science, 2016,
353,
933-936.
|
 |
|
PubMed id
|
 |
|
 |
 |
|
Abstract
|
 |
|
Noroviruses (NoVs) are a leading cause of gastroenteritis globally, yet the host
factors required for NoV infection are poorly understood. We identified host
molecules that are essential for murine NoV (MNoV)-induced cell death, including
CD300lf as a proteinaceous receptor. We found that CD300lf is essential for MNoV
binding and replication in cell lines and primary cells. Additionally,
Cd300lf(-/-) mice are resistant to MNoV infection. Expression of CD300lf in
human cells breaks the species barrier that would otherwise restrict MNoV
replication. The crystal structure of the CD300lf ectodomain reveals a potential
ligand-binding cleft composed of residues that are critical for MNoV infection.
Therefore, the presence of a proteinaceous receptor is the primary determinant
of MNoV species tropism, whereas other components of cellular machinery required
for NoV replication are conserved between humans and mice.
|
 |
|
|
|
|
 |