Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/22100
Full metadata record
DC FieldValueLanguage
dc.contributor.authorAdu-Gyamfi, Emmanuelen
dc.contributor.authorJohnson, Kristen Aen
dc.contributor.authorFraser, Mark Een
dc.contributor.authorScott, Jordan Len
dc.contributor.authorSoni, Smita Pen
dc.contributor.authorJones, Keaton Ren
dc.contributor.authorGratton, Enricoen
dc.contributor.authorTessier, Charles Ren
dc.contributor.authorStahelina, Robert Ven
dc.contributor.authorDigman, Michelleen
dc.date.accessioned2017-11-06T10:28:00Z-
dc.date.issued2015-
dc.identifier.citationJournal of Virology, 89(18), p. 9440-9453en
dc.identifier.issn1098-5514en
dc.identifier.urihttps://hdl.handle.net/1959.11/22100-
dc.description.abstractLipid-enveloped viruses replicate and bud from the host cell where they acquire their lipid coat. Ebola virus, which buds from the plasma membrane of the host cell, causes viral hemorrhagic fever and has a high fatality rate. To date, little has been known about how budding and egress of Ebola virus are mediated at the plasma membrane. We have found that the lipid phosphatidylserine (PS) regulates the assembly of Ebola virus matrix protein VP40. VP40 binds PS-containing membranes with nanomolar affinity, and binding of PS regulates VP40 localization and oligomerization on the plasma membrane inner leaflet. Further, alteration of PS levels in mammalian cells inhibits assembly and egress of VP40. Notably, interactions of VP40 with the plasma membrane induced exposure of PS on the outer leaflet of the plasma membrane at sites of egress, whereas PS is typically found only on the inner leaflet. Taking the data together, we present a model accounting for the role of plasma membrane PS in assembly of Ebola virus-like particles.en
dc.languageenen
dc.publisherAmerican Society for Microbiologyen
dc.relation.ispartofJournal of Virologyen
dc.titleHost Cell Plasma Membrane Phosphatidylserine Regulates the Assembly and Budding of Ebola Virusen
dc.typeJournal Articleen
dc.identifier.doi10.1128/JVI.01087-15en
dcterms.accessRightsGreenen
dc.subject.keywordsCell Physiologyen
dc.subject.keywordsBiochemistry and Cell Biologyen
dc.subject.keywordsBiological Physicsen
local.contributor.firstnameEmmanuelen
local.contributor.firstnameKristen Aen
local.contributor.firstnameMark Een
local.contributor.firstnameJordan Len
local.contributor.firstnameSmita Pen
local.contributor.firstnameKeaton Ren
local.contributor.firstnameEnricoen
local.contributor.firstnameCharles Ren
local.contributor.firstnameRobert Ven
local.contributor.firstnameMichelleen
local.subject.for2008029901 Biological Physicsen
local.subject.for2008111601 Cell Physiologyen
local.subject.for2008060199 Biochemistry and Cell Biology not elsewhere classifieden
local.subject.seo2008970106 Expanding Knowledge in the Biological Sciencesen
local.profile.schoolSchool of Science and Technologyen
local.profile.emailegratton@une.edu.auen
local.profile.emailmdigman@une.edu.auen
local.output.categoryC1en
local.record.placeauen
local.record.institutionUniversity of New Englanden
local.identifier.epublicationsrecordune-chute-20171103-120410en
local.publisher.placeUnited States of Americaen
local.format.startpage9440en
local.format.endpage9453en
local.url.openhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542376/en
local.peerreviewedYesen
local.identifier.volume89en
local.identifier.issue18en
local.access.fulltextYesen
local.contributor.lastnameAdu-Gyamfien
local.contributor.lastnameJohnsonen
local.contributor.lastnameFraseren
local.contributor.lastnameScotten
local.contributor.lastnameSonien
local.contributor.lastnameJonesen
local.contributor.lastnameGrattonen
local.contributor.lastnameTessieren
local.contributor.lastnameStahelinaen
local.contributor.lastnameDigmanen
dc.identifier.staffune-id:egrattonen
dc.identifier.staffune-id:mdigmanen
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.identifier.unepublicationidune:22290en
local.identifier.handlehttps://hdl.handle.net/1959.11/22100en
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
local.title.maintitleHost Cell Plasma Membrane Phosphatidylserine Regulates the Assembly and Budding of Ebola Virusen
local.output.categorydescriptionC1 Refereed Article in a Scholarly Journalen
local.search.authorAdu-Gyamfi, Emmanuelen
local.search.authorJohnson, Kristen Aen
local.search.authorFraser, Mark Een
local.search.authorScott, Jordan Len
local.search.authorSoni, Smita Pen
local.search.authorJones, Keaton Ren
local.search.authorGratton, Enricoen
local.search.authorTessier, Charles Ren
local.search.authorStahelina, Robert Ven
local.search.authorDigman, Michelleen
local.uneassociationUnknownen
local.year.published2015en
local.subject.for2020510501 Biological physicsen
local.subject.for2020320801 Cell physiologyen
local.subject.for2020310199 Biochemistry and cell biology not elsewhere classifieden
local.subject.seo2020280102 Expanding knowledge in the biological sciencesen
Appears in Collections:Journal Article
Files in This Item:
2 files
File Description SizeFormat 
Show simple item record

SCOPUSTM   
Citations

66
checked on Nov 25, 2023

Page view(s)

1,140
checked on Sep 24, 2023

Download(s)

2
checked on Sep 24, 2023
Google Media

Google ScholarTM

Check

Altmetric


Items in Research UNE are protected by copyright, with all rights reserved, unless otherwise indicated.