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About:
Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
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document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC
Creator
Fouchier, Ron
Osterhaus, Albert
Thiel, Volker
Dijkman, Ronald
Drosten, Christian
Rottier, Peter
Muth, Doreen
Mou, Huihui
Haagmans, Bart
Müller, Marcel
Berend, Jan
Bosch,
Smits, Saskia
Stalin Raj, V
Zaki, Ali
Dekkers, Dick
Demmers, Jeroen
Source
Medline; PMC
abstract
Most human coronaviruses cause mild upper respiratory tract disease but may be associated with more severe pulmonary disease in immunocompromised individuals(1). However, SARS coronavirus caused severe lower respiratory disease with nearly 10% mortality and evidence of systemic spread(2). Recently, another coronavirus (human coronavirus-Erasmus Medical Center (hCoV-EMC)) was identified in patients with severe and sometimes lethal lower respiratory tract infection(3,4). Viral genome analysis revealed close relatedness to coronaviruses found in bats(5). Here we identify dipeptidyl peptidase 4 (DPP4; also known as CD26) as a functional receptor for hCoV-EMC. DPP4 specifically co-purified with the receptor-binding S1 domain of the hCoV-EMC spike protein from lysates of susceptible Huh-7 cells. Antibodies directed against DPP4 inhibited hCoV-EMC infection of primary human bronchial epithelial cells and Huh-7 cells. Expression of human and bat (Pipistrellus pipistrellus) DPP4 in non-susceptible COS-7 cells enabled infection by hCoV-EMC. The use of the evolutionarily conserved DPP4 protein from different species as a functional receptor provides clues about the host range potential of hCoV-EMC. In addition, it will contribute critically to our understanding of the pathogenesis and epidemiology of this emerging human coronavirus, and may facilitate the development of intervention strategies. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/nature12005) contains supplementary material, which is available to authorized users.
has issue date
2013-03-13
(
xsd:dateTime
)
bibo:doi
10.1038/nature12005
bibo:pmid
23486063
has license
no-cc
sha1sum (hex)
ac25bd72e693215c9be92673f2ff7d927b052ecf
schema:url
https://doi.org/10.1038/nature12005
resource representing a document's title
Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC
has PubMed Central identifier
PMC7095326
has PubMed identifier
23486063
schema:publication
Nature
resource representing a document's body
covid:ac25bd72e693215c9be92673f2ff7d927b052ecf#body_text
is
schema:about
of
named entity 'HUMAN CORONAVIRUS'
named entity 'IS A'
named entity 'RECEPTOR'
named entity 'DIPEPTIDYL PEPTIDASE 4'
named entity 'EMC'
named entity 'FUNCTIONAL'
named entity 'functional'
named entity 'receptor'
named entity 'cell surface receptor'
named entity 'bat'
named entity 'enzyme'
named entity 'bat'
named entity 'protein'
named entity 'antiserum'
named entity 'bat'
named entity 'eluent'
named entity 'NSP4'
named entity 'coronaviruses'
named entity 'DPP4'
named entity 'ACE2'
named entity 'antiserum'
named entity 'precleared'
named entity 'downregulation'
named entity 'Coronaviruses'
named entity 'cytopathic effects'
named entity 'TaqMan'
named entity 'infection'
named entity 'cell lysates'
named entity 'serum'
named entity 'ACE2'
named entity 'expression vector'
named entity 'cell adhesion molecules'
named entity 'FITC'
named entity 'receptor'
named entity 'hormones'
named entity 'kDa'
named entity 'DPP4'
named entity 'ACE2'
named entity 'prostate'
named entity 'bat'
named entity 'receptor'
named entity 'aminopeptidase'
named entity 'DPP4'
named entity 'SARS-CoV'
named entity 'DPP4'
named entity 'cross-reactive'
named entity 'plasmid'
named entity 'DPP4'
named entity 'Huh-7'
named entity 'supernatant'
named entity 'transfection'
named entity 'SARS-CoV'
named entity '293T cells'
named entity 'lower respiratory tract'
named entity 'human coronavirus'
named entity 'antibodies'
named entity 'DPP4'
named entity 'Vero cells'
named entity 'protein'
named entity 'Taqman'
named entity 'human coronavirus'
named entity 'ciliated cells'
named entity 'antiserum'
named entity 'Pipistrellus pipistrellus'
named entity 'peptides'
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