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Encapsidation of Different Plasmonic Gold Nanoparticles by the CCMV CP
Different types of gold nanoparticles have been synthesized that show great potential in medical applications such as medical imaging, bio-analytical sensing and photothermal cancer therapy. However, their stability, polydispersity and biocompatibility are major issues of concern. For example, the s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7321416/ https://www.ncbi.nlm.nih.gov/pubmed/32516956 http://dx.doi.org/10.3390/molecules25112628 |
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author | Durán-Meza, Ana L. Escamilla-Ruiz, Martha I. Segovia-González, Xochitl F. Villagrana-Escareño, Maria V. Vega-Acosta, J. Roger Ruiz-Garcia, Jaime |
author_facet | Durán-Meza, Ana L. Escamilla-Ruiz, Martha I. Segovia-González, Xochitl F. Villagrana-Escareño, Maria V. Vega-Acosta, J. Roger Ruiz-Garcia, Jaime |
author_sort | Durán-Meza, Ana L. |
collection | PubMed |
description | Different types of gold nanoparticles have been synthesized that show great potential in medical applications such as medical imaging, bio-analytical sensing and photothermal cancer therapy. However, their stability, polydispersity and biocompatibility are major issues of concern. For example, the synthesis of gold nanorods, obtained through the elongated micelle process, produce them with a high positive surface charge that is cytotoxic, while gold nanoshells are unstable and break down in a few weeks due to the Ostwald ripening process. In this work, we report the self-assembly of the capsid protein (CP) of cowpea chlorotic mottle virus (CCMV) around spherical gold nanoparticles, gold nanorods and gold nanoshells to form virus-like particles (VLPs). All gold nanoparticles were synthesized or treated to give them a negative surface charge, so they can interact with the positive N-terminus of the CP leading to the formation of the VLPs. To induce the protein self-assembly around the negative gold nanoparticles, we use different pH and ionic strength conditions determined from a CP phase diagram. The encapsidation with the viral CP will provide the nanoparticles better biocompatibility, stability, monodispersity and a new biological substrate on which can be introduced ligands toward specific cells, broadening the possibilities for medical applications. |
format | Online Article Text |
id | pubmed-7321416 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73214162020-06-29 Encapsidation of Different Plasmonic Gold Nanoparticles by the CCMV CP Durán-Meza, Ana L. Escamilla-Ruiz, Martha I. Segovia-González, Xochitl F. Villagrana-Escareño, Maria V. Vega-Acosta, J. Roger Ruiz-Garcia, Jaime Molecules Article Different types of gold nanoparticles have been synthesized that show great potential in medical applications such as medical imaging, bio-analytical sensing and photothermal cancer therapy. However, their stability, polydispersity and biocompatibility are major issues of concern. For example, the synthesis of gold nanorods, obtained through the elongated micelle process, produce them with a high positive surface charge that is cytotoxic, while gold nanoshells are unstable and break down in a few weeks due to the Ostwald ripening process. In this work, we report the self-assembly of the capsid protein (CP) of cowpea chlorotic mottle virus (CCMV) around spherical gold nanoparticles, gold nanorods and gold nanoshells to form virus-like particles (VLPs). All gold nanoparticles were synthesized or treated to give them a negative surface charge, so they can interact with the positive N-terminus of the CP leading to the formation of the VLPs. To induce the protein self-assembly around the negative gold nanoparticles, we use different pH and ionic strength conditions determined from a CP phase diagram. The encapsidation with the viral CP will provide the nanoparticles better biocompatibility, stability, monodispersity and a new biological substrate on which can be introduced ligands toward specific cells, broadening the possibilities for medical applications. MDPI 2020-06-05 /pmc/articles/PMC7321416/ /pubmed/32516956 http://dx.doi.org/10.3390/molecules25112628 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Durán-Meza, Ana L. Escamilla-Ruiz, Martha I. Segovia-González, Xochitl F. Villagrana-Escareño, Maria V. Vega-Acosta, J. Roger Ruiz-Garcia, Jaime Encapsidation of Different Plasmonic Gold Nanoparticles by the CCMV CP |
title | Encapsidation of Different Plasmonic Gold Nanoparticles by the CCMV CP |
title_full | Encapsidation of Different Plasmonic Gold Nanoparticles by the CCMV CP |
title_fullStr | Encapsidation of Different Plasmonic Gold Nanoparticles by the CCMV CP |
title_full_unstemmed | Encapsidation of Different Plasmonic Gold Nanoparticles by the CCMV CP |
title_short | Encapsidation of Different Plasmonic Gold Nanoparticles by the CCMV CP |
title_sort | encapsidation of different plasmonic gold nanoparticles by the ccmv cp |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7321416/ https://www.ncbi.nlm.nih.gov/pubmed/32516956 http://dx.doi.org/10.3390/molecules25112628 |
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