Abstract
The newly emerged Middle East respiratory syndrome coronavirus (MERS-CoV) is becoming another "SARS-like" threat to the world. It has an extremely high death rate (∼50%) as there is no vaccine or efficient therapeutics. The identification of the structures of both the MERS-CoV receptor binding domain (RBD) and its complex with dipeptidyl peptidase 4 (DPP4), raises the hope of alleviating this currently severe situation. In this review, we examined the molecular basis of the RBD-receptor interaction to outline why/how could we use MERS-CoV RBD to develop vaccines and antiviral drugs.
Keywords:
Middle East; coronavirus; drug design; vaccines.
Copyright © 2013. Published by Elsevier B.V.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Antiviral Agents / chemistry*
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Antiviral Agents / therapeutic use
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Coronavirus / chemistry
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Coronavirus / immunology*
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Coronavirus / metabolism
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Coronavirus Infections / drug therapy
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Coronavirus Infections / immunology
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Coronavirus Infections / prevention & control
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Coronavirus Infections / virology*
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Dipeptidyl Peptidase 4 / chemistry
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Dipeptidyl Peptidase 4 / immunology*
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Dipeptidyl Peptidase 4 / metabolism
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Drug Design*
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Humans
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Receptors, Virus / chemistry
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Receptors, Virus / immunology*
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Receptors, Virus / metabolism
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Viral Vaccines / chemistry*
Substances
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Antiviral Agents
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Receptors, Virus
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Viral Vaccines
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Dipeptidyl Peptidase 4