Hierarchical peroxiredoxin assembly through orthogonal pH-response and electrostatic interactions

被引:2
作者
Anaya-Plaza, Eduardo [1 ]
Ozdemir, Zulal [2 ]
Wimmer, Zdenek [2 ]
Kostiainen, Mauri A. [1 ]
机构
[1] Aalto Univ, Sch Chem Engn, Dept Bioprod & Biosyst, Kemistintie 1, Espoo, Finland
[2] Univ Chem & Technol Prague, Dept Chem Nat Cpds, Technicka 5, Prague 6, Czech Republic
基金
芬兰科学院;
关键词
PROTEIN CRYSTALS; ACCURATE DESIGN; PORPHYRIN; NANOPARTICLES; AGGREGATION; RING;
D O I
10.1039/d3tb00369h
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Morpheeins are proteins that adapt their morphology and function to the environment. Therefore, their use in nanotechnology opens up the bottom-up preparation of anisotropic metamaterials, based on the sequential use of different stimuli. A prominent member of this family of proteins is peroxiredoxins (Prx), with dual peroxidase and chaperone function, depending on the pH of the media. At high pH, they show a toroidal morphology that turns into tubular stacks upon acidification. While the toroidal conformers have been explored as building blocks to yield 1D and 2D structures, the obtention of higher ordered materials remain unexplored. In this research, the morpheein behaviour of Prx is exploited to yield columnar aggregates, that are subsequently self-assembled into 3D anisotropic bundles. This is achieved by electrostatic recognition between the negatively charged protein rim and a positively charged porphyrin acting as molecular glue. The subsequent and orthogonal input lead to the alignment of the monodimensional stacks side-by-side, leading to the precise assembly of this anisotropic materials. Highly ordered anisotropic assemblies of toroidal peroxiredoxin protein cage are reported by the sequential and orthogonal input of pH and chemical stimuli.
引用
收藏
页码:11544 / 11551
页数:8
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