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Review
. 2015 Feb;89(4):1954-64.
doi: 10.1128/JVI.02615-14. Epub 2014 Nov 26.

Receptor recognition mechanisms of coronaviruses: a decade of structural studies

Fang Li  1
Affiliations
Review

Receptor recognition mechanisms of coronaviruses: a decade of structural studies

Fang Li. J Virol. 2015 Feb.

Abstract

Receptor recognition by viruses is the first and essential step of viral infections of host cells. It is an important determinant of viral host range and cross-species infection and a primary target for antiviral intervention. Coronaviruses recognize a variety of host receptors, infect many hosts, and are health threats to humans and animals. The receptor-binding S1 subunit of coronavirus spike proteins contains two distinctive domains, the N-terminal domain (S1-NTD) and the C-terminal domain (S1-CTD), both of which can function as receptor-binding domains (RBDs). S1-NTDs and S1-CTDs from three major coronavirus genera recognize at least four protein receptors and three sugar receptors and demonstrate a complex receptor recognition pattern. For example, highly similar coronavirus S1-CTDs within the same genus can recognize different receptors, whereas very different coronavirus S1-CTDs from different genera can recognize the same receptor. Moreover, coronavirus S1-NTDs can recognize either protein or sugar receptors. Structural studies in the past decade have elucidated many of the puzzles associated with coronavirus-receptor interactions. This article reviews the latest knowledge on the receptor recognition mechanisms of coronaviruses and discusses how coronaviruses have evolved their complex receptor recognition pattern. It also summarizes important principles that govern receptor recognition by viruses in general.

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Figures

FIG 1
FIG 1
Receptor recognition pattern of coronaviruses.
FIG 2
FIG 2
Crystal structures of coronavirus S1-CTDs complexed with their respective receptor. (A to D) These structures include β-genus SARS-CoV S1-CTD complexed with ACE2 (Protein Data Bank identifier [PDB ID]: 2AJF) (76) (A), β-genus MERS-CoV S1-CTD complexed with DPP4 (PDB ID: 4KR0) (77) (B), α-genus HCoV-NL63 S1-CTD complexed with ACE2 (PDB ID: 3KBH) (79) (C), and α-genus PRCV S1-CTD complexed with APN (PDB ID: 4F5C) (80) (D). In the structures of the complexes, the receptors are in green, and the cores and RBMs of S1-CTDs are in cyan and red, respectively. (E and F) The structural topologies of the four coronavirus S1-CTDs are shown as schematic illustrations, where β-strands are depicted as arrows and α-helices as cylinders. In the tertiary structures and structural topologies of the S1-CTDs, the secondary structures of all of the S1-CTDs are colored and numbered in the same way as for HCoV-NL63 S1-CTD.
FIG 3
FIG 3
Virus-binding hot spots on ACE2 that are critical for the binding of SARS-CoV and HCoV-NL63. (A) Enlarged view of the SARS-CoV–ACE2 interface. VBMs on ACE2 and RBM on SARS-CoV S1-CTD are in blue and red, respectively. (B) Footprint of SARS-CoV on the surface of ACE2. The view is derived from the one in panel A by rotating ACE2 by 90° along a horizontal axis in such a way that the edge facing the viewer moves up. VBM1 residues are in orange, VBM2 residues in magenta, VBM3 residues in red, and VBM1b residues in green. (C) A virus-binding hot spot on ACE2 centering on Lys31 is critical for the binding of SARS-CoV S1-CTD. Mutation of residue 479 on SARS-CoV S1-CTD is critical for the transmission of SARS-CoV from palm civets to humans. (D) A second virus-binding hot spot on ACE2 centering on Lys353 is also critical for the binding of SARS-CoV S1-CTD. Mutation of residue 487 on SARS-CoV S1-CTD is critical for the transmission of SARS-CoV from human to human. (E) Enlarged view of the HCoV-NL63–ACE2 interface. (F) Footprint of HCoV-NL63 on the surface of ACE2. (G) The same virus-binding hot spot on ACE2 centering on Lys353 is also critical for the binding of HCoV-NL63 S1-CTD.
FIG 4
FIG 4
Proposed origin and evolution of coronavirus S1-CTDs. The question mark indicates possible tertiary structures of γ-coronavirus S1-CTD.
FIG 5
FIG 5
Crystal structures of coronavirus S1-NTDs. (A and B) These structures include β-genus MHV S1-NTD complexed with its receptor CEACAM1 (PDB ID: 3R4D) (81) (A) and β-genus BCoV S1-NTD by itself (PDB ID: 4H14) (53) (B). (C) The structure of human galectin-3 (PDB ID: 1A3K) is shown as a comparison. In the structure of the MHV S1-NTD-CEACAM1 complex, the VBM on CEACAM1 and the RBM on MHV S1-NTD are in blue and red, respectively. In the structure of BCoV S1-NTD, the sugar-binding pocket as identified by mutagenesis studies is indicated by a five-pointed star. (D and E) The structural topologies of the two coronavirus S1-NTDs (D) and human galectin-3 (E) are shown as schematic illustrations, where β-strands are depicted as arrows and α-helices as cylinders. In the structural topologies of these proteins, the secondary structures are colored and numbered in the same way as for the MHV S1-NTD.
FIG 6
FIG 6
Proposed origin and evolution of coronavirus S1-NTDs. Orange arrows indicate the locations of CEACAM1 or sugar that binds coronavirus NTDs. Question marks indicate the postulated structures of hypothetical evolutionary intermediates.
FIG 7
FIG 7
Summary of the receptor recognition mechanisms of coronaviruses in a three-dimensional view. The overall structure of trimeric SARS-CoV spike complexed with ACE2 is shown; it includes both the schematic topology of the spike and the negative-stain electron micropic images of the spike ectodomain (upper right). TM, transmembrane anchor. IC, intracellular tail. The structures and functions of coronavirus S1 domains are listed. The question marks indicate possible tertiary structures of coronavirus S1 domains.
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