ACS Nano · 2019 · 38 citations · 39 references
Natural SciencesBioengineeringMaterials ScienceBiomaterialsBiomechanicsMechanobiologyBiopolymer NetworksFibrous ProteinsNanostructured BiomaterialsPolymer NetworksSupramolecular PolymersTissue MechanicsCollagen NanofibersCollagen NetworksMechanical Properties Of Fibrous ProteinsNonlinear ElasticitySupramolecular NetworksSupramolecular Polymer NetworksTensile StrengthTriple Helix Structure
Collagen is the most abundant structural protein in soft tissues, and the duplication of its structure and mechanics represents a key challenge to nanotechnology. Here we report a fibrous supramolecular network that can mimic nearly all of the aspects of collagen from dynamic hierarchical architecture to nonlinear mechanical behavior. This complex self-assembly system is solely based on a glucose polymer: curdlan, which is synthesized by bacteria and can form a similar triple helix as collagen. Triggered by solvent and temperature cues, free curdlan chains wind into superhelical trimers, and the trimers then bundle hexagonally into nanofibers of 20-40 nm in diameter. The fibers are interconnected in a water-rich 3D network structure. The network is highly dynamic and stress-responsive, which can shift from isotropic to anisotropic organization by the winding/unwinding of stress-induced interfiber triple helical net-points. Mechanical tests show that these nanofiber networks exhibit similar nonlinear elasticity as collagenous tissues including skin and tendon. The supramolecular networks also display a very wide range of tensile strength from ∼60 KPa to ∼50 MPa depending on the specific network organization. These biomimetic and dynamic supernetworks may have applications in tissue engineering, drug delivery systems, artificial skin, and soft robotics.
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