Abstract
Peptide vaccines use antigenic peptide fragments to induce an immune response but are problematic because of the short half-life of peptides. A study now reports thioamide substitution in the peptide backbone as a strategy to enhance resistance to proteolysis and promote binding to the MHC I complex for T cell activation.
Original language | English |
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Pages (from-to) | 549-550 |
Number of pages | 2 |
Journal | Nature Chemical Biology |
Volume | 20 |
Issue number | 5 |
DOIs |
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State | Published - May 2024 |