University of Hertfordshire

  • Mire Zloh
  • C. Ramaswamy
  • A. Wilderspin
  • T. Sakthivel
  • A.T. Florence
View graph of relations
Original languageEnglish
Pages (from-to)47-52
Number of pages6
JournalMagnetic Resonance in Chemistry
Volume43
Issue1
DOIs
Publication statusPublished - 1 Jan 2005

Abstract

The cationic peptide dendrons synthesized and studied are lower generation polylysine-based partial dendrimers with or without lipid chains in the core. The dendrons with lipidic chains can be utilized as protein and liposomal mimics because of their unique structural properties. The full assignments of three different dendrons (L)(NH), (C )(L)(NH) and (C)(L)(NH) were obtained in DO and HO/DO using a 500 MHz NMR spectrometer. The hydrophobic lipidic core of branched polylysine dendrons was found to induce aggregation upon increasing concentration. Because non-lipidic dendrons do not self-assemble, the behaviour and internal structural features of two different dendrons with one and three C hydrocarbon chains were explored. The critical association concentration clearly depends on the number of core hydrophobic residues and the association starts at 0.025 mM for (C)(L)(NH) and 0.05 mM for (C)(L)(NH). Chemical shift analysis also revealed that the hydrophobic chains of the dendrons associate in the core, whereas the polar head groups (NH) are mainly located at the surfaces of the aggregates. The T relaxation time measurements showed that the mobility of the hydrocarbon chain is greater with the monomeric form of dendron (C) (L)(NH) than that of monomer (C)(L)(NH). The inter-chain hydrophobic interactions restrict the flexibility of the dendron with three hydrocarbon chains. As expected, the flexibility of the monomeric form is higher than that of the aggregated state for both of the dendrons.

ID: 1447961