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Download fileMetal-Tunable Self-Assembly of Hierarchical Structure in Mussel-Inspired Peptide Films
journal contribution
posted on 2018-01-31, 00:00 authored by Franziska Jehle, Peter Fratzl, Matthew J. HarringtonBottom-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.
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Mussel byssal threadsassembly processmagnitude increaseMussel-Inspired Peptide Films Bottom-up controlpH-triggered self-assembly pointmetal coordinationbyssal thread proteinsHierarchical Structureprotein building blocksfunctionlength scalesmaterial stiffnessacid sequencemetal ionsprotein-based biofibersMetal-Tunable Self-Assemblymaterials fabricationmetal complexationpeptide films