ARC Centre of Excellence in Convergent Bio-Nano Science and Technology, Department of Chemical Engineering, The University of Melbourne, Parkville, Victoria, 3010, Australia.
Angew Chem Int Ed Engl. 2020 Sep 1;59(36):15618-15625. doi: 10.1002/anie.202002089. Epub 2020 Mar 20.
Functional materials composed of proteins have attracted much interest owing to the inherent and diverse functionality of proteins. However, establishing general techniques for assembling proteins into nanomaterials is challenging owing to the complex physicochemical nature and potential denaturation of proteins. Here, a simple, versatile strategy is introduced to fabricate functional protein assemblies through the interfacial assembly of proteins and polyphenols (e.g., tannic acid) on various substrates (organic, inorganic, and biological). The dominant interactions (hydrogen-bonding, hydrophobic, and ionic) between the proteins and tannic acid were elucidated; most proteins undergo multiple noncovalent stabilizing interactions with polyphenols, which can be used to engineer responsiveness into the assemblies. The proteins retain their structure and function within the assemblies, thereby enabling their use in various applications (e.g., catalysis, fluorescence imaging, and cell targeting).
由于蛋白质固有的多样性功能,由蛋白质组成的功能材料引起了广泛关注。然而,由于蛋白质复杂的物理化学性质和潜在的变性,将蛋白质组装成纳米材料的通用技术仍具有挑战性。在这里,我们提出了一种简单、通用的策略,通过在各种基底(有机、无机和生物)上的蛋白质和多酚(如单宁酸)的界面组装,来制造功能性蛋白质组装体。阐明了蛋白质与单宁酸之间的主要相互作用(氢键、疏水和离子相互作用);大多数蛋白质与多酚发生多种非共价稳定相互作用,可用于构建组装体的响应性。蛋白质在组装体中保留其结构和功能,从而可以将其用于各种应用(例如,催化、荧光成像和细胞靶向)。