A Mason-Pfizer Monkey virus Gag-GFP fusion vector allows visualization of capsid transport in live cells and demonstrates a role for microtubules
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
R01 CA027834
NCI NIH HHS - United States
R01-CA-27834
NCI NIH HHS - United States
PubMed
24386297
PubMed Central
PMC3873405
DOI
10.1371/journal.pone.0083863
PII: PONE-D-13-27186
Knihovny.cz E-zdroje
- MeSH
- biologický transport MeSH
- buněčná membrána metabolismus MeSH
- fluorescenční barviva metabolismus MeSH
- genetické vektory genetika MeSH
- genové produkty gag genetika metabolismus MeSH
- HEK293 buňky MeSH
- kapsida metabolismus MeSH
- kinetika MeSH
- lidé MeSH
- Masonův-Pfizerův opičí virus genetika metabolismus fyziologie MeSH
- mikrotubuly metabolismus virologie MeSH
- molekulární zobrazování MeSH
- pohyb MeSH
- proviry genetika metabolismus fyziologie MeSH
- rekombinantní fúzní proteiny genetika metabolismus MeSH
- sestavení viru MeSH
- transport proteinů MeSH
- viabilita buněk MeSH
- zelené fluorescenční proteiny genetika metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- fluorescenční barviva MeSH
- genové produkty gag MeSH
- rekombinantní fúzní proteiny MeSH
- zelené fluorescenční proteiny MeSH
Immature capsids of the Betaretrovirus, Mason-Pfizer Monkey virus (M-PMV), are assembled in the pericentriolar region of the cell, and are then transported to the plasma membrane for budding. Although several studies, utilizing mutagenesis, biochemistry, and immunofluorescence, have defined the role of some viral and host cells factors involved in these processes, they have the disadvantage of population analysis, rather than analyzing individual capsid movement in real time. In this study, we created an M-PMV vector in which the enhanced green fluorescent protein, eGFP, was fused to the carboxyl-terminus of the M-PMV Gag polyprotein, to create a Gag-GFP fusion that could be visualized in live cells. In order to express this fusion protein in the context of an M-PMV proviral backbone, it was necessary to codon-optimize gag, optimize the Kozak sequence preceding the initiating methionine, and mutate an internal methionine codon to one for alanine (M100A) to prevent internal initiation of translation. Co-expression of this pSARM-Gag-GFP-M100A vector with a WT M-PMV provirus resulted in efficient assembly and release of capsids. Results from fixed-cell immunofluorescence and pulse-chase analyses of wild type and mutant Gag-GFP constructs demonstrated comparable intracellular localization and release of capsids to untagged counterparts. Real-time, live-cell visualization and analysis of the GFP-tagged capsids provided strong evidence for a role for microtubules in the intracellular transport of M-PMV capsids. Thus, this M-PMV Gag-GFP vector is a useful tool for identifying novel virus-cell interactions involved in intracellular M-PMV capsid transport in a dynamic, real-time system.
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