In silico search, chemical characterization and immunogenic evaluation of amino-terminated G4-PAMAM-HIV peptide complexes using three-dimensional models of the HIV-1 gp120 protein
| Autor: | Jazmín García-Machorro, Manuel Jonathan Fragoso-Vázquez, João Rodrigues, Rolando Alberto Rodríguez-Fonseca, Nicolas Cayetano-Castro, María Ángeles Muñoz-Fernández, Saúl Rojas-Hernández, Raúl Borja-Urby, Jose L. Jimenez, Martiniano Bello, Mara Gutiérrez-Sánchez, José Correa-Basurto, Octavio Rodríguez-Cortés |
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| Rok vydání: | 2019 |
| Předmět: |
Models
Molecular Dendrimers In silico Peptide 02 engineering and technology Peptide-dendrimer complex HIV Envelope Protein gp120 01 natural sciences Epitope Faculdade de Ciências Exatas e da Engenharia Mice Colloid and Surface Chemistry Intranasal administration 0103 physical sciences Gp120 Animals Computer Simulation Physical and Theoretical Chemistry Binding site Peptide epitope chemistry.chemical_classification Mice Inbred BALB C 010304 chemical physics Immunogenicity Surfaces and Interfaces General Medicine 021001 nanoscience & nanotechnology Nylons G4-PAMAM dendrimer Biochemistry chemistry Docking (molecular) HIV-1 Female Nasal administration Nanocarriers Peptides 0210 nano-technology Biotechnology |
| Zdroj: | Repositório Científico de Acesso Aberto de Portugal Repositório Científico de Acesso Aberto de Portugal (RCAAP) instacron:RCAAP |
| ISSN: | 0927-7765 |
| Popis: | Peptide epitopes have been widely used to develop synthetic vaccines and immunotherapies. However, peptide epitopes may exhibit poor absorption or immunogenicity due to their low molecular weights. Conversely, fourth-generation polyamidoamine (G4-PAMAM) dendrimers are nonimmunogenic and relatively nontoxic synthetic nanoparticles that have been used as adjuvants and nanocarriers of small peptides and to improve nasal absorption. Based on this information, we hypothesized that the combination of intranasal immunization and G4-PAMAM dendrimers would be useful for enhancing the antibody responses of HIV-1 gp120 peptide epitopes. Therefore, we first used structural data, peptide epitope predictors and docking and MD simulations on MHC-II to identify two peptide epitopes on the CD4 binding site of HIV-1 gp120. The formation of G4-PAMAM-peptide complexes was evaluated in silico (molecular docking studies using different G4-PAMAM conformations retrieved from MD simulations as well as the MMGBSA approach) and validated experimentally (electrophoresis, 1H NMR and cryo-TEM). Next, the G4-PAMAM dendrimer-peptide complexes were administered intranasally to groups of female BALB/cJ mice. The results showed that both peptides were immunogenic at the systemic and mucosal levels (nasal and vaginal), and G4-PAMAM dendrimer-peptide complexes improved IgG and IgA responses in serum and nasal washes. Thus, G4-PAMAM dendrimers have potential for use as adjuvants and nanocarriers of peptides. |
| Databáze: | OpenAIRE |
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