This website uses cookies to give you the best user experience. If you continue
without changing your settings we'll assume you are happy to receive all RSC cookies.
You can change your cookie settings by navigating to our Privacy and Cookies page and following the instructions. These instructions
are also obtainable from the privacy link at the bottom of any RSC page.
Departamento de Química Orgánica, Centro Singular de Investigación en Química Biológica y Materiales Moleculares y Unidad Asociada al CSIC, Campus Vida, Universidad de Santiago de Compostela, 15782 Santiago de Compostela, Spain
E-mail: juanr.granja@usc.es
; Fax: (+34) 881 815704
; Tel: (+34) 881 815746
Org. Biomol. Chem., 2012,10, 8762-8766
DOI:
10.1039/C2OB26612A
Received
22 May 2012,
Accepted
20 Sep 2012
First published online
21 Sep 2012
In this study, a novel dimer-forming cyclic peptide composed exclusively by cyclic γ-amino acids with a saccharide-like outer surface is described. The antiparallel β-sheet type hydrogen bonding interactions responsible for the large association constant in non-polar solvents constitute a suitable model for a novel class of self-assembling peptide nanotubes.
Fetching data from CrossRef. This may take some time to load.
Organic & Biomolecular Chemistry
- Information Point