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Design of a Multicomponent Peptide-Woven Nanocomplex for Delivery of siRNA
We developed and tested a multicomponent peptide-woven siRNA nanocomplex (PwSN) comprising different peptides designed for efficient cellular targeting, endosomal escape, and release of siRNA. To enhance tumor-specific cellular uptake, we connected an interleukin-4 receptor-targeting peptide (I4R) t...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4338040/ https://www.ncbi.nlm.nih.gov/pubmed/25705892 http://dx.doi.org/10.1371/journal.pone.0118310 |
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author | Jun, Eunsung Kim, Soyoun Kim, Jong-Ho Cha, Kiweon So, In-Seop Son, Hye-Nam Lee, Byung-Heon Kim, Kwangmeyung Kwon, Ick Chan Kim, Sang Yoon Kim, In-San |
author_facet | Jun, Eunsung Kim, Soyoun Kim, Jong-Ho Cha, Kiweon So, In-Seop Son, Hye-Nam Lee, Byung-Heon Kim, Kwangmeyung Kwon, Ick Chan Kim, Sang Yoon Kim, In-San |
author_sort | Jun, Eunsung |
collection | PubMed |
description | We developed and tested a multicomponent peptide-woven siRNA nanocomplex (PwSN) comprising different peptides designed for efficient cellular targeting, endosomal escape, and release of siRNA. To enhance tumor-specific cellular uptake, we connected an interleukin-4 receptor-targeting peptide (I4R) to a nine-arginine peptide (9r), yielding I4R-9r. To facilitate endosomal escape, we blended endosomolytic peptides into the I4R-9r to form a multicomponent nanocomplex. Lastly, we modified 9r peptides by varying the number and positions of positive charges to obtain efficient release of siRNA from the nanocomplex in the cytosol. Using this step-wise approach for overcoming the biological challenges of siRNA delivery, we obtained an optimized PwSN with significant biological activity in vitro and in vivo. Interestingly, surface plasmon resonance analyses and three-dimensional peptide models demonstrated that our designed peptide adopted a unique structure that was correlated with faster complex disassembly and a better gene-silencing effect. These studies further elucidate the siRNA nanocomplex delivery pathway and demonstrate the applicability of our stepwise strategy to the design of siRNA carriers capable of overcoming multiple challenges and achieving efficient delivery. |
format | Online Article Text |
id | pubmed-4338040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-43380402015-03-04 Design of a Multicomponent Peptide-Woven Nanocomplex for Delivery of siRNA Jun, Eunsung Kim, Soyoun Kim, Jong-Ho Cha, Kiweon So, In-Seop Son, Hye-Nam Lee, Byung-Heon Kim, Kwangmeyung Kwon, Ick Chan Kim, Sang Yoon Kim, In-San PLoS One Research Article We developed and tested a multicomponent peptide-woven siRNA nanocomplex (PwSN) comprising different peptides designed for efficient cellular targeting, endosomal escape, and release of siRNA. To enhance tumor-specific cellular uptake, we connected an interleukin-4 receptor-targeting peptide (I4R) to a nine-arginine peptide (9r), yielding I4R-9r. To facilitate endosomal escape, we blended endosomolytic peptides into the I4R-9r to form a multicomponent nanocomplex. Lastly, we modified 9r peptides by varying the number and positions of positive charges to obtain efficient release of siRNA from the nanocomplex in the cytosol. Using this step-wise approach for overcoming the biological challenges of siRNA delivery, we obtained an optimized PwSN with significant biological activity in vitro and in vivo. Interestingly, surface plasmon resonance analyses and three-dimensional peptide models demonstrated that our designed peptide adopted a unique structure that was correlated with faster complex disassembly and a better gene-silencing effect. These studies further elucidate the siRNA nanocomplex delivery pathway and demonstrate the applicability of our stepwise strategy to the design of siRNA carriers capable of overcoming multiple challenges and achieving efficient delivery. Public Library of Science 2015-02-23 /pmc/articles/PMC4338040/ /pubmed/25705892 http://dx.doi.org/10.1371/journal.pone.0118310 Text en © 2015 Jun et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Jun, Eunsung Kim, Soyoun Kim, Jong-Ho Cha, Kiweon So, In-Seop Son, Hye-Nam Lee, Byung-Heon Kim, Kwangmeyung Kwon, Ick Chan Kim, Sang Yoon Kim, In-San Design of a Multicomponent Peptide-Woven Nanocomplex for Delivery of siRNA |
title | Design of a Multicomponent Peptide-Woven Nanocomplex for Delivery of siRNA |
title_full | Design of a Multicomponent Peptide-Woven Nanocomplex for Delivery of siRNA |
title_fullStr | Design of a Multicomponent Peptide-Woven Nanocomplex for Delivery of siRNA |
title_full_unstemmed | Design of a Multicomponent Peptide-Woven Nanocomplex for Delivery of siRNA |
title_short | Design of a Multicomponent Peptide-Woven Nanocomplex for Delivery of siRNA |
title_sort | design of a multicomponent peptide-woven nanocomplex for delivery of sirna |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4338040/ https://www.ncbi.nlm.nih.gov/pubmed/25705892 http://dx.doi.org/10.1371/journal.pone.0118310 |
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