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Nanoparticles engineered to bind cellular motors for efficient delivery
BACKGROUND: Dynein is a cytoskeletal molecular motor protein that transports cellular cargoes along microtubules. Biomimetic synthetic peptides designed to bind dynein have been shown to acquire dynamic properties such as cell accumulation and active intra- and inter-cellular motion through cell-to-...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5877387/ https://www.ncbi.nlm.nih.gov/pubmed/29602307 http://dx.doi.org/10.1186/s12951-018-0354-1 |
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author | Dalmau-Mena, Inmaculada del Pino, Pablo Pelaz, Beatriz Cuesta-Geijo, Miguel Ángel Galindo, Inmaculada Moros, María de la Fuente, Jesús M. Alonso, Covadonga |
author_facet | Dalmau-Mena, Inmaculada del Pino, Pablo Pelaz, Beatriz Cuesta-Geijo, Miguel Ángel Galindo, Inmaculada Moros, María de la Fuente, Jesús M. Alonso, Covadonga |
author_sort | Dalmau-Mena, Inmaculada |
collection | PubMed |
description | BACKGROUND: Dynein is a cytoskeletal molecular motor protein that transports cellular cargoes along microtubules. Biomimetic synthetic peptides designed to bind dynein have been shown to acquire dynamic properties such as cell accumulation and active intra- and inter-cellular motion through cell-to-cell contacts and projections to distant cells. On the basis of these properties dynein-binding peptides could be used to functionalize nanoparticles for drug delivery applications. RESULTS: Here, we show that gold nanoparticles modified with dynein-binding delivery sequences become mobile, powered by molecular motor proteins. Modified nanoparticles showed dynamic properties, such as travelling the cytosol, crossing intracellular barriers and shuttling the nuclear membrane. Furthermore, nanoparticles were transported from one cell to another through cell-to-cell contacts and quickly spread to distant cells through cell projections. CONCLUSIONS: The capacity of these motor-bound nanoparticles to spread to many cells and increasing cellular retention, thus avoiding losses and allowing lower dosage, could make them candidate carriers for drug delivery. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-018-0354-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5877387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58773872018-04-02 Nanoparticles engineered to bind cellular motors for efficient delivery Dalmau-Mena, Inmaculada del Pino, Pablo Pelaz, Beatriz Cuesta-Geijo, Miguel Ángel Galindo, Inmaculada Moros, María de la Fuente, Jesús M. Alonso, Covadonga J Nanobiotechnology Research BACKGROUND: Dynein is a cytoskeletal molecular motor protein that transports cellular cargoes along microtubules. Biomimetic synthetic peptides designed to bind dynein have been shown to acquire dynamic properties such as cell accumulation and active intra- and inter-cellular motion through cell-to-cell contacts and projections to distant cells. On the basis of these properties dynein-binding peptides could be used to functionalize nanoparticles for drug delivery applications. RESULTS: Here, we show that gold nanoparticles modified with dynein-binding delivery sequences become mobile, powered by molecular motor proteins. Modified nanoparticles showed dynamic properties, such as travelling the cytosol, crossing intracellular barriers and shuttling the nuclear membrane. Furthermore, nanoparticles were transported from one cell to another through cell-to-cell contacts and quickly spread to distant cells through cell projections. CONCLUSIONS: The capacity of these motor-bound nanoparticles to spread to many cells and increasing cellular retention, thus avoiding losses and allowing lower dosage, could make them candidate carriers for drug delivery. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-018-0354-1) contains supplementary material, which is available to authorized users. BioMed Central 2018-03-30 /pmc/articles/PMC5877387/ /pubmed/29602307 http://dx.doi.org/10.1186/s12951-018-0354-1 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Dalmau-Mena, Inmaculada del Pino, Pablo Pelaz, Beatriz Cuesta-Geijo, Miguel Ángel Galindo, Inmaculada Moros, María de la Fuente, Jesús M. Alonso, Covadonga Nanoparticles engineered to bind cellular motors for efficient delivery |
title | Nanoparticles engineered to bind cellular motors for efficient delivery |
title_full | Nanoparticles engineered to bind cellular motors for efficient delivery |
title_fullStr | Nanoparticles engineered to bind cellular motors for efficient delivery |
title_full_unstemmed | Nanoparticles engineered to bind cellular motors for efficient delivery |
title_short | Nanoparticles engineered to bind cellular motors for efficient delivery |
title_sort | nanoparticles engineered to bind cellular motors for efficient delivery |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5877387/ https://www.ncbi.nlm.nih.gov/pubmed/29602307 http://dx.doi.org/10.1186/s12951-018-0354-1 |
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