Design of coiled-coil protein-origami cages that self-assemble in vitro and in vivo

Nat Biotechnol. 2017 Nov;35(11):1094-1101. doi: 10.1038/nbt.3994. Epub 2017 Oct 16.

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.

MeSH terms

  • Models, Molecular
  • Nanostructures
  • Protein Engineering*
  • Protein Folding
  • Protein Multimerization
  • Protein Structure, Secondary
  • Proteins / chemistry*

Substances

  • Proteins