Channon Kevin J, Devlin Glyn L, Magennis Steven W, Finlayson Chris E, Tickler Anna K, Silva Carlos, MacPhee Cait E
Cavendish Laboratory, University of Cambridge, JJ Thomson Avenue, Cambridge, UK.
J Am Chem Soc. 2008 Apr 23;130(16):5487-91. doi: 10.1021/ja710310c. Epub 2008 Apr 1.
We describe the formation of self-assembling nanoscale fibrillar aggregates from a hybrid system comprising a short polypeptide conjugated to the fluorophore fluorene. The fibrils are typically unbranched, approximately 7 nm in diameter, and many microns in length. A range of techniques are used to demonstrate that the spectroscopic nature of the fluorophore is significantly altered in the fibrillar environment. Time-resolved fluorescence spectroscopy reveals changes in the guest fluorophore, consistent with energy migration and excimer formation within the fibrils. We thus demonstrate the use of self-assembling peptides to drive the assembly of a guest moiety, in which novel characteristics are observed as a consequence. We suggest that this method could be used to drive the assembly of a wide range of guests, offering the development of a variety of useful, smart nanomaterials that are able to self-assemble in a controllable and robust fashion.
我们描述了一种由与芴荧光团共轭的短肽组成的混合系统形成自组装纳米级纤维状聚集体的过程。这些纤维通常是无分支的,直径约为7纳米,长度达数微米。一系列技术被用于证明荧光团在纤维环境中的光谱性质发生了显著改变。时间分辨荧光光谱揭示了客体荧光团的变化,这与纤维内的能量迁移和准分子形成相一致。因此,我们证明了使用自组装肽来驱动客体部分的组装,由此观察到了新的特性。我们认为,这种方法可用于驱动多种客体的组装,从而开发出各种能够以可控且稳定的方式自组装的有用的智能纳米材料。