4.8 Article

Multivalent Noncovalent Interfacing and Cross-Linking of Supramolecular Tubes

期刊

ADVANCED MATERIALS
卷 34, 期 5, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202105926

关键词

chiral tubes; cross-linking; streptavidin-biotin interactions; supramolecular networks; supramolecular polymers; surface binding

资金

  1. European Union's Horizon 2020 research and innovation programme under the Marie Skodowska-Curie Grant [841150]
  2. European Research Council (ERC Consolidator Grant) [819075]
  3. China Scholarship Council (CSC)
  4. European Research Council (ERC) [819075] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Natural supramolecular filaments have the ability to cross-link with each other and interface with cellular membranes through biomolecular noncovalent interactions, forming complex networks. Artificial supramolecular polymers have limited exploration in specific noncovalent interactions but can be engineered to create adjustable structures by controlling surface density and concentration. This strategy provides a pathway for designing more complex biomimetic adaptive materials.
Natural supramolecular filaments have the ability to cross-link with each other and to interface with the cellular membrane via biomolecular noncovalent interactions. This behavior allows them to form complex networks within as well as outside the cell, i.e., the cytoskeleton and the extracellular matrix, respectively. The potential of artificial supramolecular polymers to interact through specific noncovalent interactions has so far only seen limited exploration due to the dynamic nature of supramolecular interactions. Here, a system of synthetic supramolecular tubes that cross-link forming supramolecular networks, and at the same time bind to biomimetic surfaces by the aid of noncovalent streptavidin-biotin linkages, is demonstrated. The architecture of the networks can be engineered by controlling the density of the biotin moiety at the exterior of the tubes as well as by the concentration of the streptavidin. The presented strategy provides a pathway for designing adjustable artificial supramolecular superstructures, which can potentially yield more complex biomimetic adaptive materials.

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