Designing Two-Dimensional Protein Arrays through Fusion of Multimers and Interface Mutations

Nano Lett. 2015 Aug 12;15(8):5235-9. doi: 10.1021/acs.nanolett.5b01499. Epub 2015 May 26.

Abstract

We have combined fusion of oligomers with cyclic symmetry and alanine substitutions to eliminate clashes and produce proteins that self-assemble into 2-D arrays upon addition of calcium ions. Using TEM, AFM, small-angle X-ray scattering, and fluorescence microscopy, we show that the designed lattices which are 5 nm high with p3 space group symmetry and 7.25 nm periodicity self-assemble into structures that can exceed 100 μm in characteristic length. The versatile strategy, experimental approach, and hexagonal arrays described herein should prove valuable for the engineering of functional nanostructured materials in 2-D.

Keywords: 2-D materials; Protein design; artificial S-layers; bionanotechnology; self-assembly.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amino Acid Substitution*
  • Bacterial Proteins / chemistry*
  • Bacterial Proteins / genetics*
  • Calcium / chemistry*
  • Microscopy, Atomic Force
  • Microscopy, Fluorescence
  • Models, Molecular
  • Nanostructures / chemistry
  • Nanostructures / ultrastructure*
  • Protein Array Analysis* / instrumentation
  • Salmonella typhimurium / chemistry
  • Salmonella typhimurium / genetics*
  • X-Ray Diffraction

Substances

  • Bacterial Proteins
  • Calcium