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Engineering multifunctional metal/protein hybrid nanomaterials as tools for therapeutic intervention and high-sensitivity detection

Protein-based hybrid nanomaterials have recently emerged as promising platforms to fabricate tailored multifunctional biologics for biotechnological and biomedical applications. This work shows a simple, modular, and versatile strategy to design custom protein hybrid nanomaterials. This approach com...

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Autores principales: Aires, Antonio, Maestro, David, Ruiz del Rio, Jorge, Palanca, Ana R., Lopez-Martinez, Elena, Llarena, Irantzu, Geraki, Kalotina, Sanchez-Cano, Carlos, Villar, Ana V., Cortajarena, Aitziber L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179251/
https://www.ncbi.nlm.nih.gov/pubmed/34164014
http://dx.doi.org/10.1039/d0sc05215a
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author Aires, Antonio
Maestro, David
Ruiz del Rio, Jorge
Palanca, Ana R.
Lopez-Martinez, Elena
Llarena, Irantzu
Geraki, Kalotina
Sanchez-Cano, Carlos
Villar, Ana V.
Cortajarena, Aitziber L.
author_facet Aires, Antonio
Maestro, David
Ruiz del Rio, Jorge
Palanca, Ana R.
Lopez-Martinez, Elena
Llarena, Irantzu
Geraki, Kalotina
Sanchez-Cano, Carlos
Villar, Ana V.
Cortajarena, Aitziber L.
author_sort Aires, Antonio
collection PubMed
description Protein-based hybrid nanomaterials have recently emerged as promising platforms to fabricate tailored multifunctional biologics for biotechnological and biomedical applications. This work shows a simple, modular, and versatile strategy to design custom protein hybrid nanomaterials. This approach combines for the first time the engineering of a therapeutic protein module with the engineering of a nanomaterial-stabilizing module within the same molecule, resulting in a multifunctional hybrid nanocomposite unachievable through conventional material synthesis methodologies. As the first proof of concept, a multifunctional system was designed ad hoc for the therapeutic intervention and monitoring of myocardial fibrosis. This hybrid nanomaterial combines a designed Hsp90 inhibitory domain and a metal nanocluster stabilizing module resulting in a biologic drug labelled with a metal nanocluster. The engineered nanomaterial actively reduced myocardial fibrosis and heart hypertrophy in an animal model of cardiac remodeling. In addition to the therapeutic effect, the metal nanocluster allowed for in vitro, ex vivo, and in vivo detection and imaging of the fibrotic disease under study. This study evidences the potential of combining protein engineering and protein-directed nanomaterial engineering approaches to design custom nanomaterials as theranostic tools, opening up unexplored routes to date for the next generation of advanced nanomaterials in medicine.
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spelling pubmed-81792512021-06-22 Engineering multifunctional metal/protein hybrid nanomaterials as tools for therapeutic intervention and high-sensitivity detection Aires, Antonio Maestro, David Ruiz del Rio, Jorge Palanca, Ana R. Lopez-Martinez, Elena Llarena, Irantzu Geraki, Kalotina Sanchez-Cano, Carlos Villar, Ana V. Cortajarena, Aitziber L. Chem Sci Chemistry Protein-based hybrid nanomaterials have recently emerged as promising platforms to fabricate tailored multifunctional biologics for biotechnological and biomedical applications. This work shows a simple, modular, and versatile strategy to design custom protein hybrid nanomaterials. This approach combines for the first time the engineering of a therapeutic protein module with the engineering of a nanomaterial-stabilizing module within the same molecule, resulting in a multifunctional hybrid nanocomposite unachievable through conventional material synthesis methodologies. As the first proof of concept, a multifunctional system was designed ad hoc for the therapeutic intervention and monitoring of myocardial fibrosis. This hybrid nanomaterial combines a designed Hsp90 inhibitory domain and a metal nanocluster stabilizing module resulting in a biologic drug labelled with a metal nanocluster. The engineered nanomaterial actively reduced myocardial fibrosis and heart hypertrophy in an animal model of cardiac remodeling. In addition to the therapeutic effect, the metal nanocluster allowed for in vitro, ex vivo, and in vivo detection and imaging of the fibrotic disease under study. This study evidences the potential of combining protein engineering and protein-directed nanomaterial engineering approaches to design custom nanomaterials as theranostic tools, opening up unexplored routes to date for the next generation of advanced nanomaterials in medicine. The Royal Society of Chemistry 2020-12-14 /pmc/articles/PMC8179251/ /pubmed/34164014 http://dx.doi.org/10.1039/d0sc05215a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Aires, Antonio
Maestro, David
Ruiz del Rio, Jorge
Palanca, Ana R.
Lopez-Martinez, Elena
Llarena, Irantzu
Geraki, Kalotina
Sanchez-Cano, Carlos
Villar, Ana V.
Cortajarena, Aitziber L.
Engineering multifunctional metal/protein hybrid nanomaterials as tools for therapeutic intervention and high-sensitivity detection
title Engineering multifunctional metal/protein hybrid nanomaterials as tools for therapeutic intervention and high-sensitivity detection
title_full Engineering multifunctional metal/protein hybrid nanomaterials as tools for therapeutic intervention and high-sensitivity detection
title_fullStr Engineering multifunctional metal/protein hybrid nanomaterials as tools for therapeutic intervention and high-sensitivity detection
title_full_unstemmed Engineering multifunctional metal/protein hybrid nanomaterials as tools for therapeutic intervention and high-sensitivity detection
title_short Engineering multifunctional metal/protein hybrid nanomaterials as tools for therapeutic intervention and high-sensitivity detection
title_sort engineering multifunctional metal/protein hybrid nanomaterials as tools for therapeutic intervention and high-sensitivity detection
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179251/
https://www.ncbi.nlm.nih.gov/pubmed/34164014
http://dx.doi.org/10.1039/d0sc05215a
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