Temperature-induced reversible self-assembly of diphenylalanine peptide and the structural transition from organogel to crystalline nanowires

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• 作者：Renliang Huang (4) (5)
  Yuefei Wang (5)
  Wei Qi (5) (6)
  Rongxin Su (5) (6)
  Zhimin He (5)
  
  4. School of Environmental Science and Engineering ; Tianjin University ; Tianjin ; 300072 ; People鈥檚 Republic of China
  5. State Key Laboratory of Chemical Engineering ; School of Chemical Engineering and Technology ; Tianjin University ; Tianjin ; 300072 ; People鈥檚 Republic of China
  6. Collaborative Innovation Center of Chemical Science and Engineering (Tianjin) ; Tianjin ; 300072 ; People鈥檚 Republic of China
  
• 关键词：Self ; assembly ; Diphenylalanine ; Peptide ; Nanowire ; Organogel
• 刊名：Nanoscale Research Letters
• 出版年：2014
• 出版时间：December 2014
• 年：2014
• 卷：9
• 期：1
• 全文大小：1,500 KB
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• 刊物主题：Nanotechnology; Nanotechnology and Microengineering; Nanoscale Science and Technology; Nanochemistry; Molecular Medicine;
• 出版者：Springer US
• ISSN：1556-276X

文摘

Controlling the self-assembly of diphenylalanine peptide (FF) into various nanoarchitectures has received great amounts of attention in recent years. Here, we report the temperature-induced reversible self-assembly of diphenylalanine peptide to microtubes, nanowires, or organogel in different solvents. We also find that the organogel in isopropanol transforms into crystalline flakes or nanowires when the temperature increases. The reversible self-assembly in polar solvents may be mainly controlled by electronic and aromatic interactions between the FF molecules themselves, which is associated with the dissociation equilibrium and significantly influenced by temperature. We found that the organogel in the isopropanol solvent made a unique transition to crystalline structures, a process that is driven by temperature and may be kinetically controlled. During the heating-cooling process, FF preferentially self-assembles to metastable nanofibers and organogel. They further transform to thermodynamically stable crystal structures via molecular rearrangement after introducing an external energy, such as the increasing temperature used in this study. The strategy demonstrated in this study provides an efficient way to controllably fabricate smart, temperature-responsive peptide nanomaterials and enriches the understanding of the growth mechanism of diphenylalanine peptide nanostructures.