Self-Assembly of the Tetraphenylethylene-Capped Diserine through a Hierarchical Assembly Process

被引:1
作者
Chang, Jui-Wen [2 ]
Chakravarthy, Rajan Deepan [2 ]
Chu, Nien-Tzu [2 ]
Liu, Jyun-Cheng [1 ]
Yeh, Mei-Yu [1 ]
Lin, Hsin-Chieh [2 ]
机构
[1] Chung Yuan Christian Univ, Dept Chem, Zhongli 320314, Taiwan
[2] Natl Yang Ming Chiao Tung Univ, Dept Mat Sci & Engn, Hsinchu 300093, Taiwan
关键词
AMPHIPHILIC PEPTIDES; HYDROGEL; NANOFIBERS; DESIGN;
D O I
10.1021/acs.bioconjchem.3c00032
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We report a new peptide-based urchin-shaped structure prepared through two-step self-assembly of tetraphenylethylenediserine (TPE-SS). Hydrogelation generated nanobelts through the first stage of self-assembly of TPE-SS; these nanobelts further transformed on silicon wafers into urchin-like microstructures featuring nanosized spines. The presence of the TPE moiety in the hydrogelator resulted in aggregation-induced emission characteristics both in the solution and in the gel phases. TPE-SS has the lowest molecular weight of any TPE-capped hydrogelator with beta-sheet-like structures under physiological pH. This new design strategy appears to be useful for generating three-dimensional self-assembled microstructures and multifunctional biomaterials. We found that TPE-SS is biocompatible with human mesenchymal stem cells and breast cancer cells, making them potential applications in tissue engineering and biomedical research.
引用
收藏
页码:562 / 571
页数:10
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