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Higher Order Architecture of Designer Peptides Forms Bioinspired 10 nm siRNA Delivery System
The higher-order architecture observed in biological systems, like viruses, is very effective in nucleic acid transport. The replications of this system has been attempted with both synthetic and naturally occurring polymers with mixed results. Here we describe a peptide/siRNA quaternary complex tha...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856157/ https://www.ncbi.nlm.nih.gov/pubmed/31728030 http://dx.doi.org/10.1038/s41598-019-53462-1 |
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author | Gamboa, Alicia Urfano, Selina F. Hernandez, Katrina Fraser, Deborah A. Ayalew, Luladey Slowinska, Katarzyna |
author_facet | Gamboa, Alicia Urfano, Selina F. Hernandez, Katrina Fraser, Deborah A. Ayalew, Luladey Slowinska, Katarzyna |
author_sort | Gamboa, Alicia |
collection | PubMed |
description | The higher-order architecture observed in biological systems, like viruses, is very effective in nucleic acid transport. The replications of this system has been attempted with both synthetic and naturally occurring polymers with mixed results. Here we describe a peptide/siRNA quaternary complex that functions as an siRNA delivery system. The rational design of a peptide assembly is inspired by the viral capsids, but not derived from them. We selected the collagen peptide (COL) to provide the structural stability and the folding framework, and hybridize it with the cell penetrating peptide (CPP) that allows for effective penetration of biological barriers. The peptide/siRNA quaternary complex forms stoichiometric, 10 nm nanoparticles, that show fast cellular uptake (<30 min), effective siRNA release, and gene silencing. The complex provides capsid-like protection for siRNA against nucleases without being immunostimulatory, or cytotoxic. Our data suggests that delivery vehicles based on synthetic quaternary structures that exhibit higher-order architecture may be effective in improving delivery and release of nucleic acid cargo. |
format | Online Article Text |
id | pubmed-6856157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68561572019-11-19 Higher Order Architecture of Designer Peptides Forms Bioinspired 10 nm siRNA Delivery System Gamboa, Alicia Urfano, Selina F. Hernandez, Katrina Fraser, Deborah A. Ayalew, Luladey Slowinska, Katarzyna Sci Rep Article The higher-order architecture observed in biological systems, like viruses, is very effective in nucleic acid transport. The replications of this system has been attempted with both synthetic and naturally occurring polymers with mixed results. Here we describe a peptide/siRNA quaternary complex that functions as an siRNA delivery system. The rational design of a peptide assembly is inspired by the viral capsids, but not derived from them. We selected the collagen peptide (COL) to provide the structural stability and the folding framework, and hybridize it with the cell penetrating peptide (CPP) that allows for effective penetration of biological barriers. The peptide/siRNA quaternary complex forms stoichiometric, 10 nm nanoparticles, that show fast cellular uptake (<30 min), effective siRNA release, and gene silencing. The complex provides capsid-like protection for siRNA against nucleases without being immunostimulatory, or cytotoxic. Our data suggests that delivery vehicles based on synthetic quaternary structures that exhibit higher-order architecture may be effective in improving delivery and release of nucleic acid cargo. Nature Publishing Group UK 2019-11-14 /pmc/articles/PMC6856157/ /pubmed/31728030 http://dx.doi.org/10.1038/s41598-019-53462-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Gamboa, Alicia Urfano, Selina F. Hernandez, Katrina Fraser, Deborah A. Ayalew, Luladey Slowinska, Katarzyna Higher Order Architecture of Designer Peptides Forms Bioinspired 10 nm siRNA Delivery System |
title | Higher Order Architecture of Designer Peptides Forms Bioinspired 10 nm siRNA Delivery System |
title_full | Higher Order Architecture of Designer Peptides Forms Bioinspired 10 nm siRNA Delivery System |
title_fullStr | Higher Order Architecture of Designer Peptides Forms Bioinspired 10 nm siRNA Delivery System |
title_full_unstemmed | Higher Order Architecture of Designer Peptides Forms Bioinspired 10 nm siRNA Delivery System |
title_short | Higher Order Architecture of Designer Peptides Forms Bioinspired 10 nm siRNA Delivery System |
title_sort | higher order architecture of designer peptides forms bioinspired 10 nm sirna delivery system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856157/ https://www.ncbi.nlm.nih.gov/pubmed/31728030 http://dx.doi.org/10.1038/s41598-019-53462-1 |
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