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Tracking morphologies at the nanoscale: self-assembly of an amphiphilic designer peptide into a double helix superstructure

机译:在纳米级跟踪形态:两亲性设计肽的自组装成双螺旋超结构

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摘要

Hierarchical self-assembly is a fundamental principle in nature, which gives rise to astonishing supramolecular architectures that offer an inspiration for the development of innovative materials in nanotechnology. Here we present the unique structure of a cone-shaped amphiphilic designer peptide. When tracking its concentration-dependent morphologies, we observed elongated bilayered single tapes at the beginning of the assembly process, which further developed into novel double-helix-like superstructures at increased concentrations. This architecture is characterized by a tight intertwisting of two individual helices, resulting in a periodic pitch size over their total lengths of several hundred nanometers. Solution X-ray scattering data revealed a marked 2-layered internal organization. All these characteristics remained unaltered for the investigated period of almost three months. In their collective morphology the assemblies are integrated into a network with hydrogel characteristics. Such a peptide based structure holds promise for a building block of next-generation nanostructured biomaterials.
机译:分层自组装是自然界中的基本原理,它产生了惊人的超分子体系结构,为纳米技术中创新材料的开发提供了灵感。在这里,我们介绍了一个锥形两亲设计器肽的独特结构。当追踪其浓度依赖性形态时,我们在组装过程开始时观察到了伸长的双层单条带,并在增加的浓度下进一步发展为新颖的双螺旋状超结构。该体系结构的特征是两个单独的螺旋紧密缠绕在一起,从而在其数百纳米的总长度上产生周期性的节距大小。溶液的X射线散射数据显示出明显的2层内部结构。在将近三个月的调查期内,所有这些特征均保持不变。在它们的集体形态下,组件被集成到具有水凝胶特征的网络中。这种基于肽的结构有望成为下一代纳米结构生物材料的基础。

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