Self-assembly of coherently dynamic, auxetic, two-dimensional protein crystals

Article

关键词: ELECTRON-MICROSCOPY;    POISSONS RATIO;    IMAGE-ANALYSIS;    GRAPHENE;    MEMBRANE;    POLYMER;    DIFFRACTION;    RESOLUTION;    DESIGN;    ARRAYS;   

DOI  :  10.1038/nature17633

来源: SCIE

【 摘 要 】

Two-dimensional (2D) crystalline materials possess unique structural, mechanical and electronic properties(1,2) that make them highly attractive in many applications(3-5). Although there have been advances in preparing 2D materials that consist of one or a few atomic or molecular layers(6,7), bottom-up assembly of 2D crystalline materials remains a challenge and an active area of development(8-10). More challenging is the design of dynamic 2D lattices that can undergo large-scale motions without loss of crystallinity. Dynamic behaviour in porous three-dimensional (3D) crystalline solids has been exploited for stimuli-responsive functions and adaptive behaviour(11-13). As in such 3D materials, integrating flexibility and adaptiveness into crystalline 2D lattices would greatly broaden the functional scope of 2D materials. Here we report the self-assembly of unsupported, 2D protein lattices with precise spatial arrangements and patterns using a readily accessible design strategy. Three single-or double-point mutants of the C4-symmetric protein RhuA were designed to assemble via different modes of intermolecular interactions (single-disulfide, double-disulfide and metal-coordination) into crystalline 2D arrays. Owing to the flexibility of the single-disulfide interactions, the lattices of one of the variants ((C98)RhuA) are essentially defect-free and undergo substantial, but fully correlated, changes in molecular arrangement, yielding coherently dynamic 2D molecular lattices. (C98)RhuA lattices display a Poisson's ratio of -1-the lowest thermodynamically possible value for an isotropic material-making them auxetic.

【 授权许可】

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