VLPs Derived from the CCMV Plant Virus Can Directly Transfect and Deliver Heterologous Genes for Translation into Mammalian Cells
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Virus-like particles (VLPs) are being used for therapeutic developments such as vaccines and drug nanocarriers. Among these, plant virus capsids are gaining interest for the formation of VLPs because they can be safely handled and are noncytotoxic. A paradigm in virology, however, is that plant viruses cannot transfect and deliver directly their genetic material or other cargos into mammalian cells. In this work, we prepared VLPs with the CCMV capsid and the mRNA-EGFP as a cargo and reporter gene. We show, for the first time, that these plant virus-based VLPs are capable of directly transfecting different eukaryotic cell lines, without the aid of any transfecting adjuvant, and delivering their nucleic acid for translation as observed by the presence of fluorescent protein. Our results show that the CCMV capsid is a good noncytotoxic container for genome delivery into mammalian cells. © 2019 María V. Villagrana-Escareño et al.
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messenger RNA; capsid protein; green fluorescent protein; virus like particle vaccine; agar gel electrophoresis; Article; cell line; cell surface; cell viability; cowpea chlorotic mottle virus; fluorescence microscopy; gene delivery system; genetic code; genetic transfection; HEK293 cell line; HeLa cell line; hk2 cell line; human; nonhuman; plant virus; protein purification; reporter gene; RNA translation; transmission electron microscopy; viral gene delivery system; virology; virus capsid; virus like agent; virus particle; animal; Bromovirus; eukaryotic cell; gene transfer; genetic transfection; genetics; plant virus; procedures; virus assembly; Animals; Bromovirus; Capsid Proteins; Cell Line; Eukaryotic Cells; Gene Transfer Techniques; Genes, Reporter; Green Fluorescent Proteins; HeLa Cells; Humans; Plant Viruses; Transfection; Vaccines, Virus-Like Particle; Virus Assembly
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