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Natl. Acad. Sci. U.S.A."],"published-print":{"date-parts":[[2020,4,21]]},"abstract":"<jats:p>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\u2019s plasma membrane during virus entry. Here, we present a 5.8-\u00c5 cryoelectron microscopy (cryo-EM) structure of EEEV complexed with the HS analog heparin. \u201cPeripheral\u201d 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 \u201caxial\u201d 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.<\/jats:p>","DOI":"10.1073\/pnas.1910670117","type":"journal-article","created":{"date-parts":[[2020,4,3]],"date-time":"2020-04-03T19:16:53Z","timestamp":1585941413000},"page":"8890-8899","update-policy":"https:\/\/doi.org\/10.1073\/pnas.cm10313","source":"Crossref","is-referenced-by-count":42,"title":["Cryo-EM structure of eastern equine encephalitis virus in complex with heparan sulfate analogues"],"prefix":"10.1073","volume":"117","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-4625-4340","authenticated-orcid":false,"given":"Chun-Liang","family":"Chen","sequence":"first","affiliation":[{"name":"Department of Biological Sciences, Purdue University, West Lafayette, IN 47907;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S. 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