VandenBerg Michael A, Sahoo Jugal Kishore, Zou Lei, McCarthy William, Webber Matthew J
Department of Chemical & Biomolecular Engineering, University of Notre Dame, Notre Dame, Indiana 46556, United States.
ACS Nano. 2020 May 26;14(5):5491-5505. doi: 10.1021/acsnano.9b09610. Epub 2020 Apr 16.
Natural proteins traverse complex free energy landscapes to assemble into hierarchically organized structures, often through stimuli-directed kinetic pathways in response to relevant biological cues. Bioinspired strategies have sought to emulate the complexity, dynamicity, and modularity exhibited in these natural processes with synthetic analogues. However, these efforts are limited by many factors that complicate the rational design and predictable assembly of synthetic constructs, especially in aqueous environments. Herein, a model discotic amphiphile gelator is described that undergoes pathway-dependent structural maturation when exposed to varying application rates of a pH stimulus, investigated by electron microscopy, spectroscopy, and X-ray scattering techniques. Under the direction of a slowly changing pH stimulus, complex hierarchical assemblies result, characterized by mesoscale elongated "superstructure" bundles embedded in a percolated mesh of narrow nanofibers. In contrast, the assembly under a rapidly applied pH stimulus is characterized by homogeneous structures that are reminiscent of the superstructures arising from the more deliberate path, except with significantly reduced scale and concomitantly large increases in bulk rheological properties. This synthetic system bears resemblance to the pathway complexity and hierarchical ordering observed for native structures, such as collagen, and points to fundamental design principles that might be applied toward enhanced control of the properties of supramolecular self-assembly across length scales.
天然蛋白质穿越复杂的自由能景观,以组装成层次有序的结构,通常是通过响应相关生物线索的刺激导向动力学途径来实现。受生物启发的策略试图用合成类似物来模拟这些自然过程中表现出的复杂性、动态性和模块化。然而,这些努力受到许多因素的限制,这些因素使合成构建体的合理设计和可预测组装变得复杂,尤其是在水性环境中。在此,描述了一种盘状两亲性凝胶剂模型,当暴露于不同pH刺激应用速率时,它会经历依赖途径的结构成熟过程,通过电子显微镜、光谱学和X射线散射技术进行研究。在缓慢变化的pH刺激作用下,会形成复杂的层次组装体,其特征是中尺度的细长“超结构”束嵌入在由窄纳米纤维组成的渗透网中。相比之下,在快速施加pH刺激下的组装体的特征是均匀结构,这让人联想到由更精心设计的途径产生的超结构,只是规模显著减小,同时整体流变学性质大幅增加。这个合成系统与天然结构(如胶原蛋白)中观察到的途径复杂性和层次有序性相似,并指出了可能应用于跨长度尺度增强超分子自组装性质控制的基本设计原则。