Modification of fluorophore photophysics through peptide-driven self-assembly

被引:68
作者
Channon, Kevin J. [2 ]
Devlin, Glyn L. [3 ]
Magennis, Steven W. [1 ]
Finlayson, Chris E. [2 ]
Tickler, Anna K. [2 ]
Silva, Carlos [4 ]
MacPhee, Cait E. [1 ]
机构
[1] Univ Edinburgh, Sch Phys, SUPA, Edinburgh EH9 3JZ, Midlothian, Scotland
[2] Univ Cambridge, Cavendish Lab, Cambridge CB3 0HE, England
[3] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
[4] Univ Montreal, Dept Phys, Montreal, PQ H3C 3J7, Canada
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1021/ja710310c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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, similar to 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.
引用
收藏
页码:5487 / 5491
页数:5
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