4.8 Article

A chemically fueled supramolecular glue for self-healing gels

期刊

CHEMICAL SCIENCE
卷 13, 期 38, 页码 11411-11421

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2sc03691f

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资金

  1. TUM Innovation Network-RISE
  2. German Federal Ministry of Education and Research (BMBF)
  3. Max Planck Society
  4. European Research Council (ERC starting grant) [852187]
  5. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [SFB-863, 111166240]
  6. DFG [411722921]
  7. European Research Council (ERC) [852187] Funding Source: European Research Council (ERC)

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In this study, a chemically fueled peptide was designed to exhibit self-healing properties, even in the absence of dynamics in fiber assembly and disassembly. The self-healing mechanism involved the formation of new nucleation sites by chemically fueled peptide molecules upon fiber perturbation. This research contributes to narrowing the gap between biological and synthetic self-assemblies by exploring the potential application of the self-healing mechanism in more complex structures.
Chemically fueled supramolecular materials offer unique properties that include spatial and temporal control and even the ability to self-heal. Indeed, a few studies have demonstrated the ability to self-heal, however, the underlying mechanisms remain unclear. Here, we designed a peptide that forms a fibrillar network upon chemical fueling. We were surprised that the hydrogel could self-heal despite the lack of dynamics in the fiber assembly and disassembly. We explain this behavior by a mechanism that involves the chemically fueled peptide molecules that cannot self-assemble due to the lack of nucleation sites. When the fibers are perturbed, new nucleation sites form that help the assembly resulting in the healing of the damaged network. Furthermore, we generalized the behavior for other peptides. We refer to this non-assembling, chemically-fueled peptide as a molecular glue. In future work, we aim to explore whether this self-healing mechanism applies to more complex structures, narrowing the gap between biological and synthetic self-assemblies.

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