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TitleCryo-EM structure of eastern equine encephalitis virus in complex with heparan sulfate analogues.
Journal, issue, pagesProc Natl Acad Sci U S A, Vol. 117, Issue 16, Page 8890-8899, Year 2020
Publish dateApr 21, 2020
AuthorsChun-Liang Chen / S Saif Hasan / Thomas Klose / Yingyuan Sun / Geeta Buda / Chengqun Sun / William B Klimstra / Michael G Rossmann /
PubMed AbstractEastern equine encephalitis virus (EEEV), a mosquito-borne icosahedral alphavirus found mainly in North America, causes human and equine neurotropic infections. EEEV neurovirulence is influenced by ...Eastern equine encephalitis virus (EEEV), a mosquito-borne icosahedral alphavirus found mainly in North America, causes human and equine neurotropic infections. EEEV neurovirulence is influenced by the interaction of the viral envelope protein E2 with heparan sulfate (HS) proteoglycans from the host's plasma membrane during virus entry. Here, we present a 5.8-Å cryoelectron microscopy (cryo-EM) structure of EEEV complexed with the HS analog heparin. "Peripheral" HS binding sites were found to be associated with the base of each of the E2 glycoproteins that form the 60 quasi-threefold spikes (q3) and the 20 sites associated with the icosahedral threefold axes (i3). In addition, there is one HS site at the vertex of each q3 and i3 spike (the "axial" sites). Both the axial and peripheral sites are surrounded by basic residues, suggesting an electrostatic mechanism for HS binding. These residues are highly conserved among EEEV strains, and therefore a change in these residues might be linked to EEEV neurovirulence.
External linksProc Natl Acad Sci U S A / PubMed:32245806 / PubMed Central
MethodsEM (single particle)
Resolution5.2 - 5.8 Å
Structure data

20019

6odf

EMDB-20019, PDB-6odf:
EEEV glycoproteins bound with heparan sulfate
Method: EM (single particle) / Resolution: 5.8 Å

EMDB-20025:
Eastern equine encephalitis virus (EEEV)
Method: EM (single particle) / Resolution: 5.2 Å

Source
  • eastern equine encephalitis virus
KeywordsVIRUS / EEEV

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