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Trifaceted Mickey Mouse Amphiphiles for Programmable Self‐Assembly, DNA Complexation and Organ‐Selective Gene Delivery
Instilling segregated cationic and lipophilic domains with an angular disposition in a trehalose‐based trifaceted macrocyclic scaffold allows engineering patchy molecular nanoparticles leveraging directional interactions that emulate those controlling self‐assembling processes in viral capsids. The...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361672/ https://www.ncbi.nlm.nih.gov/pubmed/33882160 http://dx.doi.org/10.1002/chem.202100832 |
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author | Carbajo‐Gordillo, Ana I. González‐Cuesta, Manuel Jiménez Blanco, José L. Benito, Juan M. Santana‐Armas, María L. Carmona, Thais Di Giorgio, Christophe Przybylski, Cédric Ortiz Mellet, Carmen Tros de Ilarduya, Conchita Mendicuti, Francisco García Fernández, José M. |
author_facet | Carbajo‐Gordillo, Ana I. González‐Cuesta, Manuel Jiménez Blanco, José L. Benito, Juan M. Santana‐Armas, María L. Carmona, Thais Di Giorgio, Christophe Przybylski, Cédric Ortiz Mellet, Carmen Tros de Ilarduya, Conchita Mendicuti, Francisco García Fernández, José M. |
author_sort | Carbajo‐Gordillo, Ana I. |
collection | PubMed |
description | Instilling segregated cationic and lipophilic domains with an angular disposition in a trehalose‐based trifaceted macrocyclic scaffold allows engineering patchy molecular nanoparticles leveraging directional interactions that emulate those controlling self‐assembling processes in viral capsids. The resulting trilobular amphiphilic derivatives, featuring a Mickey Mouse architecture, can electrostatically interact with plasmid DNA (pDNA) and further engage in hydrophobic contacts to promote condensation into transfectious nanocomplexes. Notably, the topology and internal structure of the cyclooligosaccharide/pDNA co‐assemblies can be molded by fine‐tuning the valency and characteristics of the cationic and lipophilic patches, which strongly impacts the transfection efficacy in vitro and in vivo. Outstanding organ selectivities can then be programmed with no need of incorporating a biorecognizable motif in the formulation. The results provide a versatile strategy for the construction of fully synthetic and perfectly monodisperse nonviral gene delivery systems uniquely suited for optimization schemes by making cyclooligosaccharide patchiness the focus. |
format | Online Article Text |
id | pubmed-8361672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83616722021-08-17 Trifaceted Mickey Mouse Amphiphiles for Programmable Self‐Assembly, DNA Complexation and Organ‐Selective Gene Delivery Carbajo‐Gordillo, Ana I. González‐Cuesta, Manuel Jiménez Blanco, José L. Benito, Juan M. Santana‐Armas, María L. Carmona, Thais Di Giorgio, Christophe Przybylski, Cédric Ortiz Mellet, Carmen Tros de Ilarduya, Conchita Mendicuti, Francisco García Fernández, José M. Chemistry Full Papers Instilling segregated cationic and lipophilic domains with an angular disposition in a trehalose‐based trifaceted macrocyclic scaffold allows engineering patchy molecular nanoparticles leveraging directional interactions that emulate those controlling self‐assembling processes in viral capsids. The resulting trilobular amphiphilic derivatives, featuring a Mickey Mouse architecture, can electrostatically interact with plasmid DNA (pDNA) and further engage in hydrophobic contacts to promote condensation into transfectious nanocomplexes. Notably, the topology and internal structure of the cyclooligosaccharide/pDNA co‐assemblies can be molded by fine‐tuning the valency and characteristics of the cationic and lipophilic patches, which strongly impacts the transfection efficacy in vitro and in vivo. Outstanding organ selectivities can then be programmed with no need of incorporating a biorecognizable motif in the formulation. The results provide a versatile strategy for the construction of fully synthetic and perfectly monodisperse nonviral gene delivery systems uniquely suited for optimization schemes by making cyclooligosaccharide patchiness the focus. John Wiley and Sons Inc. 2021-05-26 2021-06-25 /pmc/articles/PMC8361672/ /pubmed/33882160 http://dx.doi.org/10.1002/chem.202100832 Text en © 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Carbajo‐Gordillo, Ana I. González‐Cuesta, Manuel Jiménez Blanco, José L. Benito, Juan M. Santana‐Armas, María L. Carmona, Thais Di Giorgio, Christophe Przybylski, Cédric Ortiz Mellet, Carmen Tros de Ilarduya, Conchita Mendicuti, Francisco García Fernández, José M. Trifaceted Mickey Mouse Amphiphiles for Programmable Self‐Assembly, DNA Complexation and Organ‐Selective Gene Delivery |
title | Trifaceted Mickey Mouse Amphiphiles for Programmable Self‐Assembly, DNA Complexation and Organ‐Selective Gene Delivery |
title_full | Trifaceted Mickey Mouse Amphiphiles for Programmable Self‐Assembly, DNA Complexation and Organ‐Selective Gene Delivery |
title_fullStr | Trifaceted Mickey Mouse Amphiphiles for Programmable Self‐Assembly, DNA Complexation and Organ‐Selective Gene Delivery |
title_full_unstemmed | Trifaceted Mickey Mouse Amphiphiles for Programmable Self‐Assembly, DNA Complexation and Organ‐Selective Gene Delivery |
title_short | Trifaceted Mickey Mouse Amphiphiles for Programmable Self‐Assembly, DNA Complexation and Organ‐Selective Gene Delivery |
title_sort | trifaceted mickey mouse amphiphiles for programmable self‐assembly, dna complexation and organ‐selective gene delivery |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361672/ https://www.ncbi.nlm.nih.gov/pubmed/33882160 http://dx.doi.org/10.1002/chem.202100832 |
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