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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
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.
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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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