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Exosome engineering for efficient intracellular delivery of soluble proteins using optically reversible protein–protein interaction module
Nanoparticle-mediated delivery of functional macromolecules is a promising method for treating a variety of human diseases. Among nanoparticles, cell-derived exosomes have recently been highlighted as a new therapeutic strategy for the in vivo delivery of nucleotides and chemical drugs. Here we desc...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4961865/ https://www.ncbi.nlm.nih.gov/pubmed/27447450 http://dx.doi.org/10.1038/ncomms12277 |
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author | Yim, Nambin Ryu, Seung-Wook Choi, Kyungsun Lee, Kwang Ryeol Lee, Seunghee Choi, Hojun Kim, Jeongjin Shaker, Mohammed R. Sun, Woong Park, Ji-Ho Kim, Daesoo Do Heo, Won Choi, Chulhee |
author_facet | Yim, Nambin Ryu, Seung-Wook Choi, Kyungsun Lee, Kwang Ryeol Lee, Seunghee Choi, Hojun Kim, Jeongjin Shaker, Mohammed R. Sun, Woong Park, Ji-Ho Kim, Daesoo Do Heo, Won Choi, Chulhee |
author_sort | Yim, Nambin |
collection | PubMed |
description | Nanoparticle-mediated delivery of functional macromolecules is a promising method for treating a variety of human diseases. Among nanoparticles, cell-derived exosomes have recently been highlighted as a new therapeutic strategy for the in vivo delivery of nucleotides and chemical drugs. Here we describe a new tool for intracellular delivery of target proteins, named ‘exosomes for protein loading via optically reversible protein–protein interactions' (EXPLORs). By integrating a reversible protein–protein interaction module controlled by blue light with the endogenous process of exosome biogenesis, we are able to successfully load cargo proteins into newly generated exosomes. Treatment with protein-loaded EXPLORs is shown to significantly increase intracellular levels of cargo proteins and their function in recipient cells in vitro and in vivo. These results clearly indicate the potential of EXPLORs as a mechanism for the efficient intracellular transfer of protein-based therapeutics into recipient cells and tissues. |
format | Online Article Text |
id | pubmed-4961865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49618652016-09-06 Exosome engineering for efficient intracellular delivery of soluble proteins using optically reversible protein–protein interaction module Yim, Nambin Ryu, Seung-Wook Choi, Kyungsun Lee, Kwang Ryeol Lee, Seunghee Choi, Hojun Kim, Jeongjin Shaker, Mohammed R. Sun, Woong Park, Ji-Ho Kim, Daesoo Do Heo, Won Choi, Chulhee Nat Commun Article Nanoparticle-mediated delivery of functional macromolecules is a promising method for treating a variety of human diseases. Among nanoparticles, cell-derived exosomes have recently been highlighted as a new therapeutic strategy for the in vivo delivery of nucleotides and chemical drugs. Here we describe a new tool for intracellular delivery of target proteins, named ‘exosomes for protein loading via optically reversible protein–protein interactions' (EXPLORs). By integrating a reversible protein–protein interaction module controlled by blue light with the endogenous process of exosome biogenesis, we are able to successfully load cargo proteins into newly generated exosomes. Treatment with protein-loaded EXPLORs is shown to significantly increase intracellular levels of cargo proteins and their function in recipient cells in vitro and in vivo. These results clearly indicate the potential of EXPLORs as a mechanism for the efficient intracellular transfer of protein-based therapeutics into recipient cells and tissues. Nature Publishing Group 2016-07-22 /pmc/articles/PMC4961865/ /pubmed/27447450 http://dx.doi.org/10.1038/ncomms12277 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Yim, Nambin Ryu, Seung-Wook Choi, Kyungsun Lee, Kwang Ryeol Lee, Seunghee Choi, Hojun Kim, Jeongjin Shaker, Mohammed R. Sun, Woong Park, Ji-Ho Kim, Daesoo Do Heo, Won Choi, Chulhee Exosome engineering for efficient intracellular delivery of soluble proteins using optically reversible protein–protein interaction module |
title | Exosome engineering for efficient intracellular delivery of soluble proteins using optically reversible protein–protein interaction module |
title_full | Exosome engineering for efficient intracellular delivery of soluble proteins using optically reversible protein–protein interaction module |
title_fullStr | Exosome engineering for efficient intracellular delivery of soluble proteins using optically reversible protein–protein interaction module |
title_full_unstemmed | Exosome engineering for efficient intracellular delivery of soluble proteins using optically reversible protein–protein interaction module |
title_short | Exosome engineering for efficient intracellular delivery of soluble proteins using optically reversible protein–protein interaction module |
title_sort | exosome engineering for efficient intracellular delivery of soluble proteins using optically reversible protein–protein interaction module |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4961865/ https://www.ncbi.nlm.nih.gov/pubmed/27447450 http://dx.doi.org/10.1038/ncomms12277 |
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