Ayres Lee, Adams P Hans H M, Löwik Dennis W P M, van Hest Jan C M
Organic Chemistry Department, Institute for Molecules and Materials (IMM), Radboud University Nijmegen, Toernooiveld 1, Nijmegen 6525 ED, The Netherlands.
Biomacromolecules. 2005 Mar-Apr;6(2):825-31. doi: 10.1021/bm049421p.
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.
丝绸是一类经过广泛研究的天然存在的结构蛋白。特别是拖牵丝,因其强度和韧性的卓越结合而被视为自然界的高性能材料。这些机械性能源于蛋白质二级结构,即由定义明确的β-折叠片在定义不太明确的富含甘氨酸的基质中组合而成。将这种结构转化为合成聚合物是本研究的目标。为实现这一目标,合成了一种基于肽的单体,其包含丙氨酸-甘氨酸-丙氨酸-甘氨酸序列,这是在丝绸中发现的一种著名的形成β-折叠片的序列。使用原子转移自由基聚合和双功能引发剂,制备了一种定义明确的基于肽的聚合物,并将其用作甲基丙烯酸甲酯聚合的大分子引发剂。使用红外光谱对所得的定义明确的三嵌段共聚物进行分析,结果清楚地表明已引入了β-折叠片二级结构。