Receptor and viral determinants of SARS-coronavirus adaptation to human ACE2

Autor: Jianhua Sui, Wenhui Li, Wayne A. Marasco, Michael Farzan, Yaqing He, Hyeryun Choe, I-Chueh Huang, Yi Guan, Natalya Vasilieva, Jens H. Kuhn, Shiwen Luo, Chengsheng Zhang, Akikazu Murakami, Keming Xu, Swee-Kee Wong, Michael Moore
Jazyk: angličtina
Rok vydání: 2005
Předmět:
Models
Molecular

Recombinant Fusion Proteins
Molecular Sequence Data
Sequence alignment
Carboxypeptidases
Plasma protein binding
Peptidyl-Dipeptidase A
medicine.disease_cause
Article
General Biochemistry
Genetics and Molecular Biology

Disease Outbreaks
Protein structure
Viral Envelope Proteins
Viverridae
Catalytic Domain
medicine
Animals
Humans
Amino Acid Sequence
Binding site
skin and connective tissue diseases
Molecular Biology
Peptide sequence
Coronavirus
Binding Sites
Membrane Glycoproteins
General Immunology and Microbiology
biology
General Neuroscience
fungi
Outbreak
Angiotensin-converting enzyme 2
biology.organism_classification
Virology
Protein Structure
Tertiary

Rats
body regions
Severe acute respiratory syndrome-related coronavirus
Viral adaptation
Severe acute respiratory syndrome
Civet
Spike Glycoprotein
Coronavirus

Sequence Alignment
hormones
hormone substitutes
and hormone antagonists

Protein Binding
Zdroj: The EMBO Journal
Popis: Human angiotensin-converting enzyme 2 (ACE2) is a functional receptor for SARS coronavirus (SARS-CoV). Here we identify the SARS-CoV spike (S)-protein-binding site on ACE2. We also compare S proteins of SARS-CoV isolated during the 2002-2003 SARS outbreak and during the much less severe 2003-2004 outbreak, and from palm civets, a possible source of SARS-CoV found in humans. All three S proteins bound to and utilized palm-civet ACE2 efficiently, but the latter two S proteins utilized human ACE2 markedly less efficiently than did the S protein obtained during the earlier human outbreak. The lower affinity of these S proteins could be complemented by altering specific residues within the S-protein-binding site of human ACE2 to those of civet ACE2, or by altering S-protein residues 479 and 487 to residues conserved during the 2002-2003 outbreak. Collectively, these data describe molecular interactions important to the adaptation of SARS-CoV to human cells, and provide insight into the severity of the 2002-2003 SARS epidemic. © 2005 European Molecular Biology Organization | All Rights Reserved.
published_or_final_version
Databáze: OpenAIRE