Abstract
Peptide-based vaccines are composed of minimal microbial components that are required to stimulate immune responses. Peptide antigens are easy to produce, relatively cheap and non-toxic. They are also able to activate the immune system in a well-controlled manner. However, peptides themselves are poor immunogens and have to be co-administered with an adjuvant (immune stimulator) to produce desired immune responses. Unfortunately, many adjuvants are toxic, poorly effective or not compatible with peptide antigens. Recently, we demonstrated that, upon conjugation to a peptide antigen, poly(hydrophobic amino acids) can self-assemble into nanoparticles and induce strong humoral immune responses. Here, we examine the ability of polyphenylalanine to act as a self-adjuvanting moiety when conjugated to a peptide antigen derived from Group A Streptococcus M-protein. The polyphenylalanine moiety was further lipidated to alter the conjugate conformation and its ability to form nanoparticles. The lipidated analogue triggered the production of a high level of antibodies in immunized mice. The antibodies produced were highly opsonic against tested GAS clinical isolates.
| Original language | English |
|---|---|
| Pages (from-to) | 429-436 |
| Number of pages | 8 |
| Journal | Australian Journal of Chemistry |
| Volume | 76 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - Aug 2023 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- adjuvant
- amino acid polymers
- epitope conformation
- Group A Streptococcus
- nanoparticles
- opsonic antibodies
- peptide self-assembly
- peptide vaccine
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