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A novel delivery platform based on Bacteriophage MS2 virus-like particles

Our objective here is to review the novel delivery platform based on Bacteriophage MS2 virus-like particles (VLPs), including introduction to their structure, their potential as a delivery platform, and their expected use in medicine and other fields. Bacteriophage MS2 VLPs are nanoparticles devoid...

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Detalles Bibliográficos
Autores principales: Fu, Yu, Li, Jinming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114531/
https://www.ncbi.nlm.nih.gov/pubmed/26415756
http://dx.doi.org/10.1016/j.virusres.2015.08.022
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author Fu, Yu
Li, Jinming
author_facet Fu, Yu
Li, Jinming
author_sort Fu, Yu
collection PubMed
description Our objective here is to review the novel delivery platform based on Bacteriophage MS2 virus-like particles (VLPs), including introduction to their structure, their potential as a delivery platform, and their expected use in medicine and other fields. Bacteriophage MS2 VLPs are nanoparticles devoid of viral genetic material and can self-assemble from the coat protein into an icosahedral capsid. As a novel delivery platform, they possess numerous features that make them suitable and attractive for targeted delivery of RNAs or DNAs, epitope peptides, and drugs within the protein capsid. In short, as a novel delivery platform, MS2 VLPs are suitable for delivery of targeted agents and hold promise for use in diagnostics, vaccines, and therapeutic modalities.
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spelling pubmed-71145312020-04-02 A novel delivery platform based on Bacteriophage MS2 virus-like particles Fu, Yu Li, Jinming Virus Res Review Our objective here is to review the novel delivery platform based on Bacteriophage MS2 virus-like particles (VLPs), including introduction to their structure, their potential as a delivery platform, and their expected use in medicine and other fields. Bacteriophage MS2 VLPs are nanoparticles devoid of viral genetic material and can self-assemble from the coat protein into an icosahedral capsid. As a novel delivery platform, they possess numerous features that make them suitable and attractive for targeted delivery of RNAs or DNAs, epitope peptides, and drugs within the protein capsid. In short, as a novel delivery platform, MS2 VLPs are suitable for delivery of targeted agents and hold promise for use in diagnostics, vaccines, and therapeutic modalities. Elsevier B.V. 2016-01-04 2015-09-28 /pmc/articles/PMC7114531/ /pubmed/26415756 http://dx.doi.org/10.1016/j.virusres.2015.08.022 Text en Copyright © 2015 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Review
Fu, Yu
Li, Jinming
A novel delivery platform based on Bacteriophage MS2 virus-like particles
title A novel delivery platform based on Bacteriophage MS2 virus-like particles
title_full A novel delivery platform based on Bacteriophage MS2 virus-like particles
title_fullStr A novel delivery platform based on Bacteriophage MS2 virus-like particles
title_full_unstemmed A novel delivery platform based on Bacteriophage MS2 virus-like particles
title_short A novel delivery platform based on Bacteriophage MS2 virus-like particles
title_sort novel delivery platform based on bacteriophage ms2 virus-like particles
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114531/
https://www.ncbi.nlm.nih.gov/pubmed/26415756
http://dx.doi.org/10.1016/j.virusres.2015.08.022
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