Pathway driven self-assembly and living supramolecular polymerization in an amyloid-inspired peptide amphiphile

被引:49
|
作者
Singh, Ashmeet [1 ]
Joseph, Jojo P. [1 ]
Gupta, Deepika [1 ]
Sarkar, Indranil [1 ]
Pal, Asish [1 ]
机构
[1] Inst Nano Sci & Technol, Phase 10,Sect 64, Mohali, Punjab, India
关键词
HIERARCHICAL MICELLE ARCHITECTURES; COMPLEXITY; HYDROGELS; GROWTH;
D O I
10.1039/c8cc06266h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Peptide 1 with an A42 amyloid nucleating core demonstrates step-wise self-assembly in water. Variation of temperature or solvent composition arrests the self-assembly to give metastable nanoparticles, which undergo self-assembly on gradual increase in temperature and eventually produce kinetically controlled nanofibers and thermodynamically stable twisted helical bundles. Mechanical agitation of the fibers provided access to short seeds with narrow polydispersity index, which by mediation of seeded supramolecular polymerization establishes perfect control over the length of the nanofibers. Such pathway dependence and the length control of the supramolecular peptide nanofibers is exploited to tune the mechanical strength of the resulting hydrogel materials.
引用
收藏
页码:10730 / 10733
页数:4
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