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dc.rights.licenseCC BY — Creative Commons Attribution
dc.contributor.authorMitra, Dipanwita
dc.contributor.authorHasan, Mohammad H.
dc.contributor.authorBates, John T.
dc.contributor.authorBierdeman, Michael A.
dc.contributor.authorEderer, Dallas R.
dc.contributor.authorParmar, Rinkuben C.
dc.contributor.authorFassero, Lauren A.
dc.contributor.authorLiang, Quntao
dc.contributor.authorQiu, Hong
dc.contributor.authorTiwari, Vaibhav
dc.contributor.authorZhang, Fuming
dc.contributor.authorLinhardt, Robert J.
dc.contributor.authorSharp, Joshua S.
dc.contributor.authorWang, Lianchun
dc.contributor.authorTandon, Ritesh
dc.identifier.citationThe degree of polymerization and sulfation patterns in heparan sulfate are critical determinants of cytomegalovirus entry into host cells, M. H. Hasan, D. Mitra, J. T. Bates, M. A. Bierdeman, R. C. Parmar, L. A. Fassero, Q. Liang, H. Qiu, V. Tiwari, F. Zhang, R. J. Linhardt, J. S. Sharp, L. Wang, R. Tandon, PLOS Pathogens, 17 (8), e1009803, 2021.
dc.descriptionPLOS Pathogens, 17 (8), e1009803
dc.descriptionNote : if this item contains full text it may be a preprint, author manuscript, or a Gold OA copy that permits redistribution with a license such as CC BY. The final version is available through the publisher’s platform.
dc.description.abstractSeveral enveloped viruses, including herpesviruses attach to host cells by initially interacting with cell surface heparan sulfate (HS) proteoglycans followed by specific coreceptor engagement which culminates in virus-host membrane fusion and virus entry. Interfering with HS-herpesvirus interactions has long been known to result in significant reduction in virus infectivity indicating that HS play important roles in initiating virus entry. In this study, we provide a series of evidence to prove that specific sulfations as well as the degree of polymerization (dp) of HS govern human cytomegalovirus (CMV) binding and infection. First, purified CMV extracellular virions preferentially bind to sulfated longer chain HS on a glycoarray compared to a variety of unsulfated glycosaminoglycans including unsulfated shorter chain HS. Second, the fraction of glycosaminoglycans (GAG) displaying higher dp and sulfation has a larger impact on CMV titers compared to other fractions. Third, cell lines deficient in specific glucosaminyl sulfotransferases produce significantly reduced CMV titers compared to wild-type cells and virus entry is compromised in these mutant cells. Finally, purified glycoprotein B shows strong binding to heparin, and desulfated heparin analogs compete poorly with heparin for gB binding. Taken together, these results highlight the significance of HS chain length and sulfation patterns in CMV attachment and infectivity.
dc.description.sponsorshipNational Institutes of Health
dc.publisherPublic Library of Science (PLoS)
dc.relation.ispartofThe Linhardt Research Labs Online Collection
dc.relation.ispartofRensselaer Polytechnic Institute, Troy, NY
dc.relation.ispartofPLoS Pathogens
dc.rightsAttribution 3.0 United States*
dc.subjectChemistry and chemical biology
dc.subjectChemical and biological engineering
dc.subjectBiomedical engineering
dc.titleThe degree of polymerization and sulfation patterns in heparan sulfate are critical determinants of cytomegalovirus entry into host cellsen_US
dcterms.accessRightsA full text version is available in DSpace@RPI
dcterms.accessRightsOpen Access
dc.rights.holderIn Copyright : this Item is protected by copyright and/or related rights. You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s).
dc.relation.departmentThe Linhardt Research Labs.
dc.relation.departmentThe Shirley Ann Jackson, Ph.D. Center for Biotechnology and Interdisciplinary Studies (CBIS)

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