Abstract
The angiotensin converting enzyme 2 (ACE2) has been identified as a receptor for the severe acute respiratory syndrome associated coronavirus (SARS-CoV). Here we show that ACE2 expression on cell lines correlates with susceptibility to SARS-CoV S-driven infection, suggesting that ACE2 is a major receptor for SARS-CoV. The soluble ectodomain of ACE2 specifically abrogated S-mediated infection and might therefore be exploited for the generation of inhibitors. Deletion of a major portion of the cytoplasmic domain of ACE2 had no effect on S-driven infection, indicating that this domain is not important for receptor function. Our results point to a central role of ACE2 in SARS-CoV infection and suggest a minor contribution of the cytoplasmic domain to receptor function.
MeSH Terms
Amino Acid Sequence
Angiotensin-Converting Enzyme 2
Animals
Antiviral Agents/chemistry,metabolism
Carboxypeptidases/chemistry,genetics,metabolism
Cell Line
Disease Susceptibility
Humans
Mutation
Peptidyl-Dipeptidase A
Protein Structure, Tertiary
Receptors, Virus/metabolism
SARS Virus/metabolism,pathogenicity
Sequence Alignment
Severe Acute Respiratory Syndrome/metabolism
Solubility
Viral Proteins/metabolism
Chemicals
Antiviral Agents
Receptors, Virus
Viral Proteins
Carboxypeptidases
Peptidyl-Dipeptidase A
ACE2 protein, human
Angiotensin-Converting Enzyme 2
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Hofmann Heike
Chair of Genetics, University of Erlangen-Nürnberg, 91054 Erlangen, Germany.
Geier Martina
Marzi Andrea
Krumbiegel Mandy
Peipp Matthias
Fey Georg H
Gramberg Thomas
Pöhlmann Stefan
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