Metal-Tunable Self-Assembly of Hierarchical Structure in Mussel-Inspired Peptide Films

ACS Nano. 2018 Mar 27;12(3):2160-2168. doi: 10.1021/acsnano.7b07905. Epub 2018 Feb 5.

Abstract

Bottom-up control over structural hierarchy from the nanoscale through the macroscale is a critical aspect of biological materials fabrication and function, which can inspire production of advanced materials. Mussel byssal threads are a prime example of protein-based biofibers in which hierarchical organization of protein building blocks coupled via metal complexation leads to notable mechanical behaviors, such as high toughness and self-healing. Using a natural amino acid sequence from byssal thread proteins, which functions as a pH-triggered self-assembly point, we created free-standing peptide films with complex hierarchical organization across multiple length scales that can be controlled by inclusion of metal ions (Zn2+ and Cu2+) during the assembly process. Additionally, analysis of film mechanical performance indicates that metal coordination bestows up to an order of magnitude increase in material stiffness, providing a paradigm for creating tunable polymeric materials with multiscale organizational structure.

Keywords: hierarchical architecture; metal reinforcement; mussel inspired; nanostructured material; peptide film; self-assembly.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Biomimetic Materials / chemistry
  • Biomimetics
  • Coordination Complexes / chemistry
  • Copper / chemistry*
  • Models, Molecular
  • Mytilus / chemistry*
  • Nanostructures / chemistry*
  • Nanotechnology
  • Peptides / chemistry*
  • Zinc / chemistry*

Substances

  • Coordination Complexes
  • Peptides
  • Copper
  • Zinc