Abstract
A detailed study on the solid-phase synthesis of lipidated peptides of the Ras family employing the Ellman sulfonamide linker is reported. Using the C-terminal N-Ras sequence, critical issues such as lipidated amino acid resin loading, peptide elongation in the presence of labile groups and optimized conditions for release of the peptides were investigated. A versatile methodology for the synthesis of peptides with diverse lipid motifs and C-terminal methyl esters has accordingly been established.
| Original language | English |
|---|---|
| Pages (from-to) | 9585-9591 |
| Number of pages | 6 |
| Journal | Chemistry : A European Journal |
| Volume | 16 |
| Issue number | 31 |
| DOIs | |
| Publication status | Published - 2010 |
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