Please use this identifier to cite or link to this item: https://doi.org/10.1186/1743-422X-10-294
Title: Evidence for the interaction of the human metapneumovirus G and F proteins during virus-like particle formation
Authors: Loo, L.H 
Jumat, M.R
Fu, Y
Ayi, T.C
Wong, P.S
Tee, N.W.S 
Tan, B.H
Sugrue, R.J
Keywords: Human metapneumovirus f protein
Human metapneumovirus g protein
Human metapneumovirus m protein
unclassified drug
virus protein
article
electron microscopy
human
human cell
Human metapneumovirus
image analysis
mammal cell
nonhuman
nucleotide sequence
protein cross linking
protein expression
protein protein interaction
sucrose density gradient centrifugation
sucrose gradient
virus assembly
virus like agent
virus morphology
Human metapneumovirus
Mammalia
Cell Line
Centrifugation, Density Gradient
Child
Child, Preschool
Gene Expression
Glycoproteins
Humans
Metapneumovirus
Microscopy, Electron
Molecular Sequence Data
Protein Binding
Recombinant Proteins
RNA, Viral
Sequence Analysis, DNA
Viral Fusion Proteins
Viral Proteins
Virosomes
Issue Date: 2013
Citation: Loo, 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
Rights: Attribution 4.0 International
Abstract: Background: 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.
Source Title: Virology Journal
URI: https://scholarbank.nus.edu.sg/handle/10635/181801
ISSN: 1743422X
DOI: 10.1186/1743-422X-10-294
Rights: Attribution 4.0 International
Appears in Collections:Staff Publications
Elements

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_1186_1743-422X-10-294.pdf2.6 MBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons