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Plant‐derived protein bodies as delivery vehicles for recombinant proteins into mammalian cells
The encapsulation of biopharmaceuticals into micro‐ or nanoparticles is a strategy frequently used to prevent degradation or to achieve the slow release of therapeutics and vaccines. Protein bodies (PBs), which occur naturally as storage organelles in seeds, can be used as such carrier vehicles. The...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7079162/ https://www.ncbi.nlm.nih.gov/pubmed/31956981 http://dx.doi.org/10.1002/bit.27273 |
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author | Schwestka, Jennifer Tschofen, Marc Vogt, Stefan Marcel, Sylvain Grillari, Johannes Raith, Marianne Swoboda, Ines Stoger, Eva |
author_facet | Schwestka, Jennifer Tschofen, Marc Vogt, Stefan Marcel, Sylvain Grillari, Johannes Raith, Marianne Swoboda, Ines Stoger, Eva |
author_sort | Schwestka, Jennifer |
collection | PubMed |
description | The encapsulation of biopharmaceuticals into micro‐ or nanoparticles is a strategy frequently used to prevent degradation or to achieve the slow release of therapeutics and vaccines. Protein bodies (PBs), which occur naturally as storage organelles in seeds, can be used as such carrier vehicles. The fusion of the N‐terminal sequence of the maize storage protein, γ‐zein, to other proteins is sufficient to induce the formation of PBs, which can be used to bioencapsulate recombinant proteins directly in the plant production host. In addition, the immunostimulatory effects of zein have been reported, which are advantageous for vaccine delivery. However, little is known about the interaction between zein PBs and mammalian cells. To better understand this interaction, fluorescent PBs, resulting from the fusion of the N‐terminal portion of zein to a green fluorescent protein, was produced in Nicotiana benthamiana leaves, recovered by a filtration‐based downstream procedure, and used to investigate their internalization efficiency into mammalian cells. We show that fluorescent PBs were efficiently internalized into intestinal epithelial cells and antigen‐presenting cells (APCs) at a higher rate than polystyrene beads of comparable size. Furthermore, we observed that PBs stimulated cytokine secretion by epithelial cells, a characteristic that may confer vaccine adjuvant activities through the recruitment of APCs. Taken together, these results support the use of zein fusion proteins in developing novel approaches for drug delivery based on controlled protein packaging into plant PBs. |
format | Online Article Text |
id | pubmed-7079162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70791622020-03-19 Plant‐derived protein bodies as delivery vehicles for recombinant proteins into mammalian cells Schwestka, Jennifer Tschofen, Marc Vogt, Stefan Marcel, Sylvain Grillari, Johannes Raith, Marianne Swoboda, Ines Stoger, Eva Biotechnol Bioeng ARTICLES The encapsulation of biopharmaceuticals into micro‐ or nanoparticles is a strategy frequently used to prevent degradation or to achieve the slow release of therapeutics and vaccines. Protein bodies (PBs), which occur naturally as storage organelles in seeds, can be used as such carrier vehicles. The fusion of the N‐terminal sequence of the maize storage protein, γ‐zein, to other proteins is sufficient to induce the formation of PBs, which can be used to bioencapsulate recombinant proteins directly in the plant production host. In addition, the immunostimulatory effects of zein have been reported, which are advantageous for vaccine delivery. However, little is known about the interaction between zein PBs and mammalian cells. To better understand this interaction, fluorescent PBs, resulting from the fusion of the N‐terminal portion of zein to a green fluorescent protein, was produced in Nicotiana benthamiana leaves, recovered by a filtration‐based downstream procedure, and used to investigate their internalization efficiency into mammalian cells. We show that fluorescent PBs were efficiently internalized into intestinal epithelial cells and antigen‐presenting cells (APCs) at a higher rate than polystyrene beads of comparable size. Furthermore, we observed that PBs stimulated cytokine secretion by epithelial cells, a characteristic that may confer vaccine adjuvant activities through the recruitment of APCs. Taken together, these results support the use of zein fusion proteins in developing novel approaches for drug delivery based on controlled protein packaging into plant PBs. John Wiley and Sons Inc. 2020-01-30 2020-04 /pmc/articles/PMC7079162/ /pubmed/31956981 http://dx.doi.org/10.1002/bit.27273 Text en © 2020 The Authors. Biotechnology and Bioengineering published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | ARTICLES Schwestka, Jennifer Tschofen, Marc Vogt, Stefan Marcel, Sylvain Grillari, Johannes Raith, Marianne Swoboda, Ines Stoger, Eva Plant‐derived protein bodies as delivery vehicles for recombinant proteins into mammalian cells |
title | Plant‐derived protein bodies as delivery vehicles for recombinant proteins into mammalian cells |
title_full | Plant‐derived protein bodies as delivery vehicles for recombinant proteins into mammalian cells |
title_fullStr | Plant‐derived protein bodies as delivery vehicles for recombinant proteins into mammalian cells |
title_full_unstemmed | Plant‐derived protein bodies as delivery vehicles for recombinant proteins into mammalian cells |
title_short | Plant‐derived protein bodies as delivery vehicles for recombinant proteins into mammalian cells |
title_sort | plant‐derived protein bodies as delivery vehicles for recombinant proteins into mammalian cells |
topic | ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7079162/ https://www.ncbi.nlm.nih.gov/pubmed/31956981 http://dx.doi.org/10.1002/bit.27273 |
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