| Literature DB >> 15762647 |
Lee Ayres1, P Hans H M Adams, Dennis W P M Löwik, Jan C M van Hest.
Abstract
Silks are a widely studied class of naturally occurring structural proteins. Dragline spider silk, in particular, is considered to be nature's high-performance material due to its remarkable combination of strength and toughness. These mechanical properties stem from the protein secondary structure, a combination of well-defined beta-sheets in a less well-defined glycine-rich matrix. The translation of this structure into a synthetic polymer was the aim of this investigation. To achieve this, a peptide-based monomer containing the sequence alanine-glycine-alanine-glycine, a well-known beta-sheet-forming sequence found in silk, was synthesized. Using atom-transfer radical polymerization and a bifunctional initiator, a well-defined peptide-based polymer was prepared. This was then used as the macroinitiator for the polymerization of methyl methacrylate. The resulting well-defined triblock copolymer was analyzed using IR spectroscopy, which clearly showed beta-sheet secondary structure had been introduced.Entities:
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Year: 2005 PMID: 15762647 DOI: 10.1021/bm049421p
Source DB: PubMed Journal: Biomacromolecules ISSN: 1525-7797 Impact factor: 6.988