van Doremalen_2016_J.Virol_90_5499

Reference

Title : Mapping the Specific Amino Acid Residues That Make Hamster DPP4 Functional as a Receptor for Middle East Respiratory Syndrome Coronavirus - van Doremalen_2016_J.Virol_90_5499
Author(s) : van Doremalen N , Miazgowicz KL , Munster VJ
Ref : J Virol , 90 :5499 , 2016
Abstract :

UNLABELLED: The novel emerging coronavirus Middle East respiratory syndrome coronavirus (MERS-CoV) binds to its receptor, dipeptidyl peptidase 4 (DPP4), via 14 interacting amino acids. We previously showed that if the five interacting amino acids which differ between hamster and human DPP4 are changed to the residues found in human DPP4, hamster DPP4 does act as a receptor. Here, we show that the functionality of hamster DPP4 as a receptor is severely decreased if less than 4 out of 5 amino acids are changed. IMPORTANCE: The novel emerging coronavirus MERS-CoV has infected >1,600 people worldwide, and the case fatality rate is approximately 36%. In this study, we show that by changing 4 amino acids in hamster DPP4, this protein functions as a receptor for MERS-CoV. This work is vital in the development of new small-animal models, which will broaden our understanding of MERS-CoV and be instrumental in the development of countermeasures.

PubMedSearch : van Doremalen_2016_J.Virol_90_5499
PubMedID: 27030263
Gene_locus related to this paper: human-DPP4

Related information

Gene_locus human-DPP4
Family DPP4N_Peptidase_S9

Citations formats

van Doremalen N, Miazgowicz KL, Munster VJ (2016)
Mapping the Specific Amino Acid Residues That Make Hamster DPP4 Functional as a Receptor for Middle East Respiratory Syndrome Coronavirus
J Virol 90 :5499

van Doremalen N, Miazgowicz KL, Munster VJ (2016)
J Virol 90 :5499