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Updated: May 1, 2026

Constructing Thioether/Vinyl Sulfide-tethered Helical Peptides Via Photo-induced Thiol-ene/yne Hydrothiolation
Published on: August 1, 2018
Lipidated peptides via post-synthetic thioalkylation promoted by molecular sieves
Enrica Calce1, Marilisa Leone, Luca Monfregola
1Institute of Biostructures and Bioimaging, National Research Council, 80134, Naples, Italy.
Abstract:
A thioalkylation procedure, which uses molecular sieves to promote the reaction, was exploited to provide peptides with useful functional groups (lipidic moieties), naturally occurring on proteins as post-translational modifications. The procedure was further implemented to synthesize tailor-made lipidated peptides, interesting tools to investigate biological processes involving their Ras parent proteins. Moreover, the one-pot preparation of multi-alkylated peptides confirms the versatility and flexibility of the employed methodology.

