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Co-Functionalization of Gold Nanoparticles with C7H2 and HuAL1 Peptides: Enhanced Antimicrobial and Antitumoral Activities

The functionalization of nanoparticles with therapeutic peptides has been pointed out as a promising strategy to improve the applications of these molecules in the field of health sciences. Peptides are highly bioactive but face several limitations such as low bioavailability due to the difficulty o...

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Autores principales: Formaggio, Daniela M. D., Magalhães, Jéssica A., Andrade, Vitor M., Conceição, Katia, Anastácio, Juliana M., Santiago, Gabrielli S., Arruda, Denise C., Tada, Dayane B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9317637/
https://www.ncbi.nlm.nih.gov/pubmed/35890220
http://dx.doi.org/10.3390/pharmaceutics14071324
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author Formaggio, Daniela M. D.
Magalhães, Jéssica A.
Andrade, Vitor M.
Conceição, Katia
Anastácio, Juliana M.
Santiago, Gabrielli S.
Arruda, Denise C.
Tada, Dayane B.
author_facet Formaggio, Daniela M. D.
Magalhães, Jéssica A.
Andrade, Vitor M.
Conceição, Katia
Anastácio, Juliana M.
Santiago, Gabrielli S.
Arruda, Denise C.
Tada, Dayane B.
author_sort Formaggio, Daniela M. D.
collection PubMed
description The functionalization of nanoparticles with therapeutic peptides has been pointed out as a promising strategy to improve the applications of these molecules in the field of health sciences. Peptides are highly bioactive but face several limitations such as low bioavailability due to the difficulty of overcoming the physiological barriers in the body and their degradation by enzymes. In this work, gold nanoparticles (AuNPs) were co-functionalized with two therapeutic peptides simultaneously. The peptides from the complementary determining region of monoclonal antibodies, composed of the amino acid sequences YISCYNGATSYNQKFK (C7H2) and RASQSVSSYLA (HuAL1) were chosen for having exhibited antitumor and antimicrobial activity before. The peptides-conjugated AuNPs were characterized regarding size, morphology, and metal concentration by using TEM, dynamic light scattering, and ICP-OES techniques. Then, peptides-conjugated AuNPs were evaluated regarding the antimicrobial activity against E. coli, P. aeruginosa, and C. albicans. The antitumoral activity was evaluated in vitro by cell viability assays with metastatic melanoma cell line (B16F10-Nex2) and the cytotoxicity was evaluated against human foreskin fibroblast (Hs68) cell line. Finally, in vivo assays were performed by using a syngeneic animal model of metastatic melanoma. Our findings have highlighted the potential application of the dual-peptide AuNPs in order to enhance the antitumor and antimicrobial activity of peptides.
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spelling pubmed-93176372022-07-27 Co-Functionalization of Gold Nanoparticles with C7H2 and HuAL1 Peptides: Enhanced Antimicrobial and Antitumoral Activities Formaggio, Daniela M. D. Magalhães, Jéssica A. Andrade, Vitor M. Conceição, Katia Anastácio, Juliana M. Santiago, Gabrielli S. Arruda, Denise C. Tada, Dayane B. Pharmaceutics Article The functionalization of nanoparticles with therapeutic peptides has been pointed out as a promising strategy to improve the applications of these molecules in the field of health sciences. Peptides are highly bioactive but face several limitations such as low bioavailability due to the difficulty of overcoming the physiological barriers in the body and their degradation by enzymes. In this work, gold nanoparticles (AuNPs) were co-functionalized with two therapeutic peptides simultaneously. The peptides from the complementary determining region of monoclonal antibodies, composed of the amino acid sequences YISCYNGATSYNQKFK (C7H2) and RASQSVSSYLA (HuAL1) were chosen for having exhibited antitumor and antimicrobial activity before. The peptides-conjugated AuNPs were characterized regarding size, morphology, and metal concentration by using TEM, dynamic light scattering, and ICP-OES techniques. Then, peptides-conjugated AuNPs were evaluated regarding the antimicrobial activity against E. coli, P. aeruginosa, and C. albicans. The antitumoral activity was evaluated in vitro by cell viability assays with metastatic melanoma cell line (B16F10-Nex2) and the cytotoxicity was evaluated against human foreskin fibroblast (Hs68) cell line. Finally, in vivo assays were performed by using a syngeneic animal model of metastatic melanoma. Our findings have highlighted the potential application of the dual-peptide AuNPs in order to enhance the antitumor and antimicrobial activity of peptides. MDPI 2022-06-23 /pmc/articles/PMC9317637/ /pubmed/35890220 http://dx.doi.org/10.3390/pharmaceutics14071324 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Formaggio, Daniela M. D.
Magalhães, Jéssica A.
Andrade, Vitor M.
Conceição, Katia
Anastácio, Juliana M.
Santiago, Gabrielli S.
Arruda, Denise C.
Tada, Dayane B.
Co-Functionalization of Gold Nanoparticles with C7H2 and HuAL1 Peptides: Enhanced Antimicrobial and Antitumoral Activities
title Co-Functionalization of Gold Nanoparticles with C7H2 and HuAL1 Peptides: Enhanced Antimicrobial and Antitumoral Activities
title_full Co-Functionalization of Gold Nanoparticles with C7H2 and HuAL1 Peptides: Enhanced Antimicrobial and Antitumoral Activities
title_fullStr Co-Functionalization of Gold Nanoparticles with C7H2 and HuAL1 Peptides: Enhanced Antimicrobial and Antitumoral Activities
title_full_unstemmed Co-Functionalization of Gold Nanoparticles with C7H2 and HuAL1 Peptides: Enhanced Antimicrobial and Antitumoral Activities
title_short Co-Functionalization of Gold Nanoparticles with C7H2 and HuAL1 Peptides: Enhanced Antimicrobial and Antitumoral Activities
title_sort co-functionalization of gold nanoparticles with c7h2 and hual1 peptides: enhanced antimicrobial and antitumoral activities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9317637/
https://www.ncbi.nlm.nih.gov/pubmed/35890220
http://dx.doi.org/10.3390/pharmaceutics14071324
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