蛋白质设计
螺旋线圈
蛋白质折叠
蛋白质结构
结晶学
蛋白质工程
生物物理学
四面体
体内
化学
折叠(DSP实现)
纳米技术
材料科学
生物
生物化学
酶
电气工程
工程类
生物技术
作者
Ajasja Ljubetič,Fabio Lapenta,Helena Gradišar,Igor Drobnak,Jana Aupič,Žiga Strmšek,Duško Lainšček,Iva Hafner‐Bratkovič,Andreja Majerle,Nuša Krivec,Mojca Benčina,Tomaž Pisanski,Tanja Ćirković Veličković,Adam Round,J.M. Carazo,Roberto Melero,Roman Jerala
摘要
Polypeptides and polynucleotides are natural programmable biopolymers that can self-assemble into complex tertiary structures. We describe a system analogous to designed DNA nanostructures in which protein coiled-coil (CC) dimers serve as building blocks for modular de novo design of polyhedral protein cages that efficiently self-assemble in vitro and in vivo. We produced and characterized >20 single-chain protein cages in three shapes-tetrahedron, four-sided pyramid, and triangular prism-with the largest containing >700 amino-acid residues and measuring 11 nm in diameter. Their stability and folding kinetics were similar to those of natural proteins. Solution small-angle X-ray scattering (SAXS), electron microscopy (EM), and biophysical analysis confirmed agreement of the expressed structures with the designs. We also demonstrated self-assembly of a tetrahedral structure in bacteria, mammalian cells, and mice without evidence of inflammation. A semi-automated computational design platform and a toolbox of CC building modules are provided to enable the design of protein cages in any polyhedral shape.
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