Metal-Tunable Self-Assembly of Hierarchical Structure in Mussel-Inspired Peptide Films.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 29385330.
- Also identified by DOI 10.1021/acsnano.7b07905.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
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 (Zn<sup>2+</sup> and Cu<sup>2+</sup>) 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.
Medical subject headings
- Copper
- Mytilus
- Nanostructures
- Peptides
- Zinc