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1.
Nanomedicine (Lond) ; 9(1): 35-43, 2014 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-23611619

RESUMO

AIM: To explore four-arm star poly(t-butyl)acrylate (P(t)BA)-peptide and linear P(t)BA-peptide conjugates as a vaccine-delivery system against Group A Streptococcus. MATERIALS & METHODS: P(t)BA nanoparticles bearing J14 peptide epitopes were prepared via alkyne-azide 1,3-dipolar cycloaddition 'click' reaction. The conjugated products were self-assembled into small or large nanoparticles. These nanoparticle vaccine candidates were evaluated in vivo and J14-specific antibody titers were assessed. RESULTS & DISCUSSION: Mice vaccinated with the nanoparticles were able to produce J14-specific IgG antibodies without the use of an external adjuvant after a single immunization. We have demonstrated for the first time that the immune responses against self-assembled P(t)BA nanoparticles are stronger for the smaller sized (~20 nm) nanoparticles compared with the larger (~500 nm) P(t)BA nanoparticles. CONCLUSION: PtBA analogs have the potential to be developed as potent carrier systems for single-dose synthetic vaccines.


Assuntos
Sistemas de Liberação de Medicamentos , Peptídeos/uso terapêutico , Polímeros/uso terapêutico , Vacinas/uso terapêutico , Adjuvantes Imunológicos , Animais , Epitopos/imunologia , Humanos , Imunoglobulina G/imunologia , Camundongos , Nanomedicina , Nanopartículas/química , Nanopartículas/uso terapêutico , Peptídeos/química , Peptídeos/imunologia , Polímeros/química , Vacinas/imunologia
2.
Molecules ; 18(11): 13148-74, 2013 Oct 24.
Artigo em Inglês | MEDLINE | ID: mdl-24284482

RESUMO

The copper (I)-catalyzed alkyne azide 1,3-dipolar cycloaddition (CuAAC) or 'click' reaction, is a highly versatile reaction that can be performed under a variety of reaction conditions including various solvents, a wide pH and temperature range, and using different copper sources, with or without additional ligands or reducing agents. This reaction is highly selective and can be performed in the presence of other functional moieties. The flexibility and selectivity has resulted in growing interest in the application of CuAAC in various fields. In this review, we briefly describe the importance of the structural folding of peptides and proteins and how the 1,4-disubstituted triazole product of the CuAAC reaction is a suitable isoster for an amide bond. However the major focus of the review is the application of this reaction to produce peptide conjugates for tagging and targeting purpose, linkers for multifunctional biomacromolecules, and reporter ions for peptide and protein analysis.


Assuntos
Química Click/métodos , Cobre/química , Peptídeos/química , Alcinos/química , Azidas/química , Proteínas/química
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