Literature detail

The receptor binding domain of the new Middle East respiratory syndrome coronavirus maps to a 231-residue region in the spike protein that efficiently elicits neutralizing antibodies.

Huihui Mou1 V Stalin Raj Frank J M van Kuppeveld Peter J M Rottier Bart L Haagmans Berend Jan Bosch
Affiliations 1 institutions
  1. Department of Infectious Diseases and Immunology, Virology Division, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.
PMID 23785207 2013 J Virol eng ppublish
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Article

Publication summary

The spike (S) protein of the recently emerged human Middle East respiratory syndrome coronavirus (MERS-CoV) mediates infection by binding to the cellular receptor dipeptidyl peptidase 4 (DPP4). Here we mapped the receptor binding domain in the S protein to a 231-amino-acid fragment (residues 358 to 588) by evaluating the interaction of spike truncation variants with receptor-expressing cells and soluble DPP4. Antibodies to this domain--much less so those to the preceding N-terminal region--efficiently neutralize MERS-CoV infection.

Virus Attachment Antibodies, Neutralizing Antibodies, Viral Binding Sites Cell Line Coronavirus Dipeptidyl Peptidase 4 Epitopes, B-Lymphocyte Humans Membrane Glycoproteins Receptors, Virus Spike Glycoprotein, Coronavirus Viral Envelope Proteins DPP4 protein, human spike glycoprotein, SARS-CoV spike protein, mouse hepatitis virus

Structured evidence records

Evidence records

1 total
1 records
Extraction confidence 1.00
Key finding

MERS-CoV spike protein binds to human dipeptidyl peptidase 4 (DPP4) to mediate cell entry, with the receptor binding domain located at residues 358–588 of the spike protein.

Virus
Location
Not specified
Supporting text

The spike (S) protein of the recently emerged human Middle East respiratory syndrome coronavirus (MERS-CoV) mediates infection by binding to the cellular receptor dipeptidyl peptidase 4 (DPP4). Here we mapped the receptor binding domain in the S protein to a 231-amino-acid fragment (residues 358 to 588) by evaluating the interaction of spike truncation variants with receptor-expressing cells and soluble DPP4.

Method
receptor binding assay; interaction with receptor-expressing cells; soluble receptor binding analysis
Receptors
dipeptidyl peptidase 4 (DPP4)