Issue 7, 2011

Aggregation behaviour of peptide–polymer conjugates containing linear peptide backbones and multiple polymer side chains prepared by nitroxide-mediated radical polymerization

Abstract

A series of peptides with an alternating sequence of alkoxyamine conjugated lysine and glycine residues were synthesized by classical solution phase peptide coupling. The resulting peptides containing up to eight alkoxyamine moieties were used as initiators in nitroxide-mediated polymerization (NMP) to obtain peptidepolymer conjugates with well defined linear peptide backbones and a defined number of polymeric side chains. Polymerization of styrene and N-isopropylacrylamide (NIPAM) occurred in a highly controlled fashion. Molecular weight and polydispersity index (PDI) were determined by gel permeation chromatography (GPC). Aggregation behaviour of these hybrid materials was investigated by dynamic light scattering (DLS) and atomic force microscopy (AFM). Depending on composition, number and length of the polymer side chains, the conjugates aggregate to different topologies. Whereas peptidepolystyrene conjugates may aggregate to so called honeycomb structures, peptide–poly-N-isopropylacrylamide conjugates show differentiated aggregation behaviour.

Graphical abstract: Aggregation behaviour of peptide–polymer conjugates containing linear peptide backbones and multiple polymer side chains prepared by nitroxide-mediated radical polymerization

Supplementary files

Article information

Article type
Paper
Submitted
18 Nov 2010
Accepted
07 Jan 2011
First published
14 Feb 2011

Org. Biomol. Chem., 2011,9, 2403-2412

Aggregation behaviour of peptidepolymer conjugates containing linear peptide backbones and multiple polymer side chains prepared by nitroxide-mediated radical polymerization

M. Möller, C. Hentschel, L. Chi and A. Studer, Org. Biomol. Chem., 2011, 9, 2403 DOI: 10.1039/C0OB01047B

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