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LptD-antigen system on gold nanoparticles: an innovative strategy in the nanovaccine development

Nanovaccine development is a growing research field in which the development of new carriers and bioconjugation approaches is a priority. In this sense, this report describes for the first time, the development of a novel conjugate that consists of gold nanoparticles (AuNPs) obtained by a one-step s...

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Published in:Nanotechnology 2022-07, Vol.33 (29), p.295602
Main Authors: Aguilera-Juárez, Ana, Hernández-Adame, Luis, Ruíz-Gómez, Miguel Ángel, Monreal-Escalante, Elizabeth, Reyes-Becerril, Martha, Rosales-Mendoza, Sergio, Pereyra, Héctor Gabriel Silva, Angulo, Carlos
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Language:English
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Summary:Nanovaccine development is a growing research field in which the development of new carriers and bioconjugation approaches is a priority. In this sense, this report describes for the first time, the development of a novel conjugate that consists of gold nanoparticles (AuNPs) obtained by a one-step synthesis using an immunogenic peptide of the Lipopolysaccharide-assembly protein LptD from bacteria as a reducing and capping agent. The resulting compounds were fully characterized and the results showed the high capacity of the peptide to form complexes and reduce gold ions. The reaction yield estimated was higher than 83% and the chemical integrity of the peptide on the NP surface revealed a tyrosine amino acid bonding on the AuNP surface. Furthermore, the system showed high colloidal stability in a wide pH range (3-11 pH values), where the hydrodynamic diameter and Zeta potential behavior were strongly influenced by the functional groups of the antigenic peptide. The cytotoxicity assays showed that the obtained system is safe for mouse leukocytes, while immunized mice with produced specific IgG antibodies. These encouraging results revealed the efficacy of some antigenic peptides as reducers and capping agents, in addition, opening the path to determine immunogenicity and immunoprotective efficacy of the system against the disease induced by .
ISSN:0957-4484
1361-6528
DOI:10.1088/1361-6528/ac659b