结晶学
堆积
丝带
形态学(生物学)
化学
氢键
层状结构
超分子化学
两亲性
烷基
超分子手性
二肽
自组装
分子动力学
立体化学
生物物理学
材料科学
分子
聚合物
肽
共聚物
有机化学
晶体结构
计算化学
复合材料
遗传学
生物
生物化学
作者
Yanyao Wang,Chengcheng Zhao,Taohong He,Weipeng Zhao,Annela M. Seddon,Dave J. Adams,Honghui Yang
标识
DOI:10.1021/acs.biomac.5c01528
摘要
Abundant reversible noncovalent interactions contribute greatly to the anisotropy of supramolecular morphologies and the transformation across multiple structures. However, the trigger (group) to drive the transformation remains obscure. Herein, H-bonding between free N-terminal amines of l-tryptophan derivatives (GTCn) and DMSO, triggering a morphological transition is revealed from flat to twisted nanoribbons by tuning DMSO/H2O ratios. Corresponding dynamic macroscopic morphology evolution from an aggregated cluster to a flower-like sphere of gel is observed under an optical microscope. Combined experiments and molecular dynamics (MD) simulations establish this H-bonding as the submolecular trigger, which simultaneously induces the change of π–π stacking, from the J-type to H-type. Alkyl chains at the C-terminus modulate structural dimensions, while gel thixotropy is governed by chiral morphology. These results provide a molecular strategy for precisely triggering twisted ribbon formation in self-assembly alongside the injectable chiral gel systems visible under optical microscopy.
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