超分子化学
两亲性
自组装
超分子手性
形态学(生物学)
分散性
胶束
手性(物理)
分子
纳米结构
材料科学
结晶学
纳米技术
序列(生物学)
化学工程
超分子组装
肽
化学
纳米颗粒
纳米纤维
单层
化学物理
超分子聚合物
共聚物
晶体结构
有机化学
高分子化学
物理
水溶液
聚合物
生物
量子力学
生物化学
遗传学
手征对称破缺
Nambu–Jona Lasinio模型
夸克
作者
M. Hussain Sangji,Hiroaki Sai,Stacey M. Chin,Sieun Ruth Lee,Ivan R. Sasselli,Liam C. Palmer,Samuel I. Stupp
出处
期刊:Nano Letters
[American Chemical Society]
日期:2021-07-14
卷期号:21 (14): 6146-6155
被引量:23
标识
DOI:10.1021/acs.nanolett.1c01737
摘要
The morphology of supramolecular peptide nanostructures is difficult to predict given their complex energy landscapes. We investigated peptide amphiphiles containing β-sheet forming domains that form twisted nanoribbons in water. We explained the morphology based on a balance between the energetically favorable packing of molecules in the center of the nanostructures, the unfavorable packing at the edges, and the deformations due to packing of twisted β-sheets. We find that morphological polydispersity of PA nanostructures is determined by peptide sequences, and the twisting of their internal β-sheets. We also observed a change in the supramolecular chirality of the nanostructures as the peptide sequence was modified, although only amino acids with l-configuration were used. Upon increasing charge repulsion between molecules, we observed a change in morphology to long cylinders and then rodlike fragments and spherical micelles. Understanding the self-assembly mechanisms of peptide amphiphiles into nanostructures should be useful to optimize their well-known functions.
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