Responsive gels formed by the spontaneous self-assembly of peptides into polymeric beta-sheet tapes

被引:751
作者
Aggeli, A
Bell, M
Boden, N
Keen, JN
Knowles, PF
McLeish, TCB
Pitkeathly, M
Radford, SE
机构
[1] UNIV LEEDS,CTR SELF ORGANISING MOL SYST,LEEDS LS2 9JT,W YORKSHIRE,ENGLAND
[2] UNIV LEEDS,SCH CHEM,LEEDS LS2 9JT,W YORKSHIRE,ENGLAND
[3] UNIV LEEDS,DEPT BIOCHEM & MOL BIOL,LEEDS LS2 9JT,W YORKSHIRE,ENGLAND
[4] UNIV LEEDS,DEPT PHYS,LEEDS LS2 9JT,W YORKSHIRE,ENGLAND
[5] UNIV OXFORD,OXFORD CTR MOL SCI,OXFORD OX1 3QT,ENGLAND
[6] UNIV OXFORD,NEW CHEM LAB,OXFORD OX1 3QT,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1038/386259a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Molecular self-assembly is becoming an increasingly popular route to new supramolecular structures and molecular materials(1-7). The inspiration for such structures is commonly derived from self-assembling systems in biology. Here we show that a biological motif, the peptide beta-sheet, can be exploited in designed oligopeptides that self-assemble into polymeric tapes and with potentially useful mechanical properties. We describe the construction of oligopeptides, rationally designed or based on segments of native proteins, that aggregate in suitable solvents into long, semi-flexible beta-sheet tapes. These become entangled even at low volume fractions to form gels whose viscoelastic properties can be controlled by chemical (pH) or physical (shear) influences. We suggest that it should be possible to engineer a wide range of properties in these gels by appropriate choice of the peptide primary structure.
引用
收藏
页码:259 / 262
页数:4
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