Please use this identifier to cite or link to this item: https://doi.org/10.1186/1743-422X-10-294
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dc.titleEvidence for the interaction of the human metapneumovirus G and F proteins during virus-like particle formation
dc.contributor.authorLoo, L.H
dc.contributor.authorJumat, M.R
dc.contributor.authorFu, Y
dc.contributor.authorAyi, T.C
dc.contributor.authorWong, P.S
dc.contributor.authorTee, N.W.S
dc.contributor.authorTan, B.H
dc.contributor.authorSugrue, R.J
dc.date.accessioned2020-10-28T07:18:07Z
dc.date.available2020-10-28T07:18:07Z
dc.date.issued2013
dc.identifier.citationLoo, L.H, Jumat, M.R, Fu, Y, Ayi, T.C, Wong, P.S, Tee, N.W.S, Tan, B.H, Sugrue, R.J (2013). Evidence for the interaction of the human metapneumovirus G and F proteins during virus-like particle formation. Virology Journal 10 : 294. ScholarBank@NUS Repository. https://doi.org/10.1186/1743-422X-10-294
dc.identifier.issn1743422X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181801
dc.description.abstractBackground: Human metapneumovirus (HMPV) is now a major cause of lower respiratory infection in children. Although primary isolation of HMPV has been achieved in several different cell lines, the low level of virus replication and the subsequent recovery of low levels of infectious HMPV have hampered biochemical studies on the virus. These experimental methodologies usually require higher levels of biological material that can be achieved following HMPV infection. In this study we demonstrate that expression of the HMPV F, G and M proteins in mammalian cells leads to HMPV virus-like particles (VLP) formation. This experimental strategy will serve as a model system to allow the process of HMPV virus assembly to be examined. Methods. The HMPV F, G and M proteins were expressed in mammalian cell lines. Protein cross-linking studies, sucrose gradient centrifugation and in situ imaging was used to examine interactions between the virus proteins. VLP formation was examined using sucrose density gradient centrifugation and electron microscopy analysis. Results: Analysis of cells co-expressing the F, G and M proteins demonstrated that these proteins interacted. Furthermore, in cells co-expression the three HMPV proteins the formation VLPs was observed. Image analysis revealed the VLPs had a similar morphology to the filamentous virus morphology that we observed on HMPV-infected cells. The capacity of each protein to initiate VLP formation was examined using a VLP formation assay. Individual expression of each virus protein showed that the G protein was able to form VLPs in the absence of the other virus proteins. Furthermore, co-expression of the G protein with either the M or F proteins facilitated their incorporation into the VLP fraction. Conclusion: Co-expression of the F, G and M proteins leads to the formation of VLPs, and that incorporation of the F and M proteins into VLPs is facilitated by their interaction with the G protein. Our data suggests that the G protein plays a central role in VLP formation, and further suggests that the G protein may also play a role in the recruitment of the F and M proteins to sites of virus particle formation during HMPV infection. © 2013 Loo et al.; licensee BioMed Central Ltd.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectHuman metapneumovirus f protein
dc.subjectHuman metapneumovirus g protein
dc.subjectHuman metapneumovirus m protein
dc.subjectunclassified drug
dc.subjectvirus protein
dc.subjectarticle
dc.subjectelectron microscopy
dc.subjecthuman
dc.subjecthuman cell
dc.subjectHuman metapneumovirus
dc.subjectimage analysis
dc.subjectmammal cell
dc.subjectnonhuman
dc.subjectnucleotide sequence
dc.subjectprotein cross linking
dc.subjectprotein expression
dc.subjectprotein protein interaction
dc.subjectsucrose density gradient centrifugation
dc.subjectsucrose gradient
dc.subjectvirus assembly
dc.subjectvirus like agent
dc.subjectvirus morphology
dc.subjectHuman metapneumovirus
dc.subjectMammalia
dc.subjectCell Line
dc.subjectCentrifugation, Density Gradient
dc.subjectChild
dc.subjectChild, Preschool
dc.subjectGene Expression
dc.subjectGlycoproteins
dc.subjectHumans
dc.subjectMetapneumovirus
dc.subjectMicroscopy, Electron
dc.subjectMolecular Sequence Data
dc.subjectProtein Binding
dc.subjectRecombinant Proteins
dc.subjectRNA, Viral
dc.subjectSequence Analysis, DNA
dc.subjectViral Fusion Proteins
dc.subjectViral Proteins
dc.subjectVirosomes
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1186/1743-422X-10-294
dc.description.sourcetitleVirology Journal
dc.description.volume10
dc.description.page294
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