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1.
Methods Mol Biol ; 1403: 639-53, 2016.
Article in English | MEDLINE | ID: mdl-27076158

ABSTRACT

A protein-based vaccine approach against hookworm infection has failed to deliver the expected outcome, due to a problem with an allergic response in the patient or difficulties in the proteins' production. This implication could be overcome by using a chemically synthesized peptide-based vaccine approach. This approach utilizes minimal pathogenic components that are necessary for the stimulation of the immune response without triggering adverse side effects. To boost the peptide's immunogenicity, a lipid core peptide (LCP) system can be utilized as a carrier molecule/immunostimulant. This chapter describes in detail the synthesizing of protected lipoamino acid, the self-adjuvanting moiety (LCP core), the peptide epitope, and the final vaccine candidate. The subunit peptide and the LCP core were synthesized using microwave-assisted solid-phase peptide synthesis (SPPS). Then the final hookworm vaccine construct was assembled using the copper-catalyzed azide-alkyne cycloaddition, or "click," reaction.


Subject(s)
Click Chemistry/methods , Hookworm Infections/prevention & control , Microwaves , Solid-Phase Synthesis Techniques/methods , Vaccines/chemical synthesis , Animals , Epitopes/immunology , Necator americanus/immunology , Palmitic Acid/chemistry , Vaccines/chemistry , Vaccines/immunology , Vaccines, Subunit/chemical synthesis , Vaccines, Subunit/chemistry , Vaccines, Subunit/immunology
2.
ChemMedChem ; 10(10): 1647-54, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26269385

ABSTRACT

Necator americanus (hookworm) infects over half a billion people worldwide. Anthelminthic drugs are commonly used to treat the infection; however, vaccination is a more favorable strategy to combat this parasite. We designed new B-cell peptide epitopes based on the aspartic protease of N. americanus (Na-APR-1). The peptides were conjugated to self-adjuvanting lipid core peptide (LCP) systems via stepwise solid-phase peptide synthesis (SPPS) and copper catalyst azide-alkyne cycloaddition (CuAAC) reactions. The LCP vaccine candidates were able to self-assemble into nanoparticles, were administered to mice without the use of additional adjuvant, and generated antibodies that recognized the parent epitope. However, only one LCP derivative was able to produce a high titer of antibodies specific to Na-APR-1; circular dichroism analyses of this compound showed a ß-sheet conformation for the incorporated epitope. This study provides important insight in epitope and delivery system design for the development of a vaccine against hookworm infections.


Subject(s)
Aspartic Acid Proteases/immunology , Hookworm Infections/parasitology , Lipopeptides/immunology , Nanoparticles/chemistry , Necator americanus/immunology , Vaccines, Synthetic/chemistry , Vaccines, Synthetic/immunology , Animals , Antibodies, Helminth/immunology , Aspartic Acid Proteases/chemistry , Female , Hookworm Infections/immunology , Lipopeptides/chemistry , Mice , Mice, Inbred BALB C , Molecular Conformation , Necator americanus/enzymology , Particle Size , Structure-Activity Relationship
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