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Reversible Supramolecular Assembly of Velvet Worm Adhesive Fibers via Electrostatic Interactions of Charged Phosphoproteins.
Baer, Alexander; Hänsch, Sebastian; Mayer, Georg; Harrington, Matthew J; Schmidt, Stephan.
Afiliación
  • Baer A; Department of Zoology, Institute of Biology , University of Kassel , Heinrich-Plett-Str. 40 , 34132 Kassel , Germany.
  • Hänsch S; Center for Advanced Imaging (CAi) , Heinrich-Heine-Universität Düsseldorf , Universitätsstraße 1 , 40225 Düsseldorf , Germany.
  • Mayer G; Department of Zoology, Institute of Biology , University of Kassel , Heinrich-Plett-Str. 40 , 34132 Kassel , Germany.
  • Harrington MJ; Department of Biomaterials , Max Planck Institute of Colloids and Interfaces , Potsdam 14424 , Germany.
  • Schmidt S; Department of Chemistry , McGill University , 801 Sherbrooke Street West , Montreal , Quebec H3A 0B8 , Canada.
Biomacromolecules ; 19(10): 4034-4043, 2018 10 08.
Article en En | MEDLINE | ID: mdl-30114911
ABSTRACT
Velvet worms secrete a fluid hunting slime comprised of a dispersion of nanoglobules that form microfibers under small mechanical shear forces, facilitating the rapid formation of stiff biopolymeric fibers. Here, we demonstrate that the nanoglobules are held together and stabilized as a dispersion by electrostatic interactions reminiscent of coacervate-based natural adhesives. Variation of ionic strength and pH affects the stability of nanoglobules and their ability to form fibers. Fibers mainly consist of large (∼300 kDa), highly charged proteins, and current biochemical analysis reveals a high degree of protein phosphorylation and presence of divalent cations. Taken together, we surmise that polyampholytic protein sequences, phosphorylated sites, and ions give rise to transient ionic cross-linking, enabling reversible curing of ejected slime into high-stiffness fibers following dehydration. These results provide a deeper understanding of velvet worm adhesive fibers, which may stimulate new routes toward mechanoresponsive and sustainable materials.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fosfoproteínas / Artrópodos / Adhesivos / Reactivos de Enlaces Cruzados / Nanoestructuras / Electricidad Estática / Proteínas de Artrópodos Límite: Animals Idioma: En Revista: Biomacromolecules Asunto de la revista: BIOLOGIA MOLECULAR Año: 2018 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fosfoproteínas / Artrópodos / Adhesivos / Reactivos de Enlaces Cruzados / Nanoestructuras / Electricidad Estática / Proteínas de Artrópodos Límite: Animals Idioma: En Revista: Biomacromolecules Asunto de la revista: BIOLOGIA MOLECULAR Año: 2018 Tipo del documento: Article País de afiliación: Alemania