N-linked peptidoresorc[4]arene-based receptors designed for protein surface recognition. NMR analysis of Italian virgin olive oils and structural analysis of polysaccharides.

  • CERRETO, ANTONELLA
Publication date
February 2012

Abstract

The first part of this work concerned the synthesis of N-linked peptideresorcarenes and the study of their surface interaction with enzymes. As known, an important class of protein surface receptors based on the attachment of four cyclic peptides to a calix[4]arene scaffold was developed by Hamilton and targeted to the serine protease α-chymotrypsin (ChT). Moving from Hamilton’s results and from some preliminary molecular modeling studies, valyl-leucine, leucyl-valine and valyl-aspartic peptidoresorc[4]arenes have been designed with the aim to target the predominantly cationic region surrounding the active site of ChT. By varying sequence, nature, and stereochemistry of the side chains, we prepared anionically functionalized N-linked peptid...

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