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Innovative chemical synthesis and conformational hints on the lipopeptide liraglutide

Academic Article
Publication Date:
2016
abstract:
Liraglutide is a new generation lipopeptide drug used for the treatment of type II diabetes. In this work, we describe new approaches for its preparation fully by chemical methods. The key step of these strategies is the synthesis in solution of the Lys/-Glu building block, Fmoc-Lys-(Pal--Glu-OtBu)-OH, in which Lys and Glu residues are linked through their side chains and -Glu is N-palmitoylated. This dipeptide derivative is then inserted into the peptide sequence on solid phase. As liraglutide is obtained with great purity and high yield, our approach can be particularly attractive for an industrial production. We also report here the results of a circular dichroism conformational analysis in a membrane mimetic environment that offers new insights into the mechanism of action of liraglutide. Copyright (c) 2016 European Peptide Society and John Wiley & Sons, Ltd.
Iris type:
01.01 Articolo in rivista
Keywords:
circular dichroism; conformational analysis; lipope; liraglutide; peptide synthesis
List of contributors:
Formaggio, Fernando; Toniolo, Claudio; Biondi, Barbara
Authors of the University:
BIONDI BARBARA
Handle:
https://iris.cnr.it/handle/20.500.14243/323567
Published in:
JOURNAL OF PEPTIDE SCIENCE (PRINT)
Journal
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