Biocatalytically Triggered Co-Assembly of Two-Component Core/Shell Nanofibers

被引:64
作者
Abul-Haija, Yousef M. [1 ]
Roy, Sangita [1 ]
Frederix, Pim W. J. M. [1 ]
Javid, Nadeem [1 ]
Jayawarna, Vineetha [1 ]
Ulijn, Rein V. [1 ]
机构
[1] Univ Strathclyde, Dept Pure & Appl Chem, WestCHEM, Glasgow G1 1XL, Lanark, Scotland
基金
英国工程与自然科学研究理事会;
关键词
biocatalysis; co-assembly; peptides; surface functionality; transformation; PEPTIDE-AMPHIPHILE NANOFIBERS; SUPRAMOLECULAR HYDROGELS; ENZYMATIC FORMATION; SMALL MOLECULES; BETA-SHEETS; SELF; NANOTUBES; CELLS;
D O I
10.1002/smll.201301668
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
For the development of applications and novel uses for peptide nanostructures, robust routes for their surface functionalization, that ideally do not interfere with their self-assembly properties, are required. Many existing methods rely on covalent functionalization, where building blocks are appended with functional groups, either pre- or post-assembly. A facile supramolecular approach is demonstrated for the formation of functionalized nanofibers by combining the advantages of biocatalytic self-assembly and surfactant/gelator co-assembly. This is achieved by enzymatically triggered reconfiguration of free flowing micellar aggregates of pre-gelators and functional surfactants to form nanofibers that incorporate and display the surfactants' functionality at the surface. Furthermore, by varying enzyme concentration, the gel stiffness and supramolecular organization of building blocks can be varied.
引用
收藏
页码:973 / 979
页数:7
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