Self-assembly mechanisms of nanofibers from peptide amphiphiles in solution and on substrate surfaces

被引:56
|
作者
Liao, Hsien-Shun [1 ,3 ,4 ]
Lin, Jing [2 ]
Liu, Yang [5 ]
Huang, Peng [2 ]
Jin, Albert [4 ]
Chen, Xiaoyuan [3 ]
机构
[1] Natl Taiwan Univ, Dept Mech Engn, Taipei 10617, Taiwan
[2] Shenzhen Univ, Sch Biomed Engn, Guangdong Key Lab Biomed Measurements & Ultrasoud, Shenzhen 518060, Peoples R China
[3] NIBIB, Lab Mol Imaging & Nanomed LOMIN, NIH, Bethesda, MD 20892 USA
[4] NIBIB, Lab Cellular Imaging & Macromol Biophys, NIH, Bethesda, MD 20892 USA
[5] Duke Univ, Dept Biomed Engn, Fitzpatrick Inst Photon, Durham, NC 27708 USA
基金
中国国家自然科学基金;
关键词
ATOMIC-FORCE MICROSCOPY; AMYLOID FIBRILS; ALPHA-SYNUCLEIN; MOLECULAR-DYNAMICS; CELLULAR MOTILITY; CONTACT-ANGLE; BETA PEPTIDE; NANOSTRUCTURES; DESIGN; MICROTUBULES;
D O I
10.1039/c6nr04672j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report the investigation of the self-assembly mechanism of nanofibers, using a small peptide amphiphile (NapFFKYp) as a model. Combining experimental and simulation methods, we identify the self-assembly pathways in the solution and on the substrates, respectively. In the solution, peptide amphiphiles undergo the nucleation process to grow into nanofibers. The nanofibers can further twist into high-ordered nanofibers with aging. On the substrates, peptide amphiphiles form nanofibers and nanosheet structures simultaneously. This surface-induced nanosheet consists of rod-like structures, and its thickness is substrate-dependent. Most intriguingly, water can transform the nanosheet into the nanofiber. Molecular dynamic simulation suggests that hydrophobic and ion-ion interactions are dominant forces during the self-assembly process.
引用
收藏
页码:14814 / 14820
页数:7
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