Intramolecular acyl transfer in peptide and protein ligation and synthesis‡. (30th January 2015)

• Record Type: Journal Article
• Authors: Tailhades, Julien; Patil, Nitin A.; Hossain, Mohammed Akhter; Wade, John D.
• Is Part Of: Journal of peptide science. Volume 21:Number 3(2015:Mar.)
• Page Start: 139
• Page End: 147
• Publication Date: 2015-01-30
• Subjects: Peptides -- Periodicals; Peptides -- Periodicals; 572.65
• DOI: 10.1002/psc.2749
• Languages: English
• ISSNs: 1075-2617

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Intramolecular acyl transfer equilibrium in peptides and proteins has stimulated the development of new methodologies for ligation, aggregation suppression or difficult peptide synthesis. Native chemical ligation or aggregation suppression methodologies are based on an X‐to‐N acyl transfer of a peptide chain (X = S, O). The reverse reaction from N‐to‐X has led to exciting developments in solving key synthetic problems such as peptide thioester preparation using Fmoc/tBu strategy. Depending on the target peptide or protein, variations of these methods, which are also based on acyl transfer equilibriums, are now available.</p> <p>In this review, we provide a detailed overview of development and utility of methodologies in peptide chemistry that are based on the control of intramolecular equilibrium. To this end, we outline the scaffolds that are favorable for acyl transfer, the conditions for controlling both sides of the acyl transfer equilibrium and their applications to peptide and protein chemistry. Additional new methodologies have been developed for the synthesis of difficult peptides such as peptide alcohols or head‐to‐tail cyclic peptides. Promising new applications of intramolecular acyl transfer reactions are also highlighted. Copyright © 2015 European Peptide Society and John Wiley &amp; Sons, Ltd.</p> </abstract>