| Literature DB >> 29035374 |
Ajasja Ljubetič1, Fabio Lapenta1,2, Helena Gradišar1,3, Igor Drobnak1, Jana Aupič1,4, Žiga Strmšek1, Duško Lainšček1, Iva Hafner-Bratkovič1,3, Andreja Majerle1, Nuša Krivec1, Mojca Benčina1, Tomaž Pisanski5, Tanja Ćirković Veličković6, Adam Round7,8, José María Carazo9, Roberto Melero9, Roman Jerala1,3.
Abstract
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.Entities:
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Year: 2017 PMID: 29035374 DOI: 10.1038/nbt.3994
Source DB: PubMed Journal: Nat Biotechnol ISSN: 1087-0156 Impact factor: 54.908