Keywords :
Hydrogels; Adhesives; Microgels; Polysaccharides; Animals; Gastropoda/chemistry; Gastropoda/metabolism; Polysaccharides/chemistry; Polysaccharides/metabolism; Hydrogels/chemistry; Adhesives/chemistry; Microgels/chemistry; Cross linking; Crosslinked networks; Double network gels; Double-network hydrogels; Fast setting; Gain insight; Membrane-bound; Microgel; Network mechanism; Polyanionics; Gastropoda; Chemistry (all); Condensed Matter Physics
Abstract :
[en] The slug Arion subfuscus produces a tough, highly adhesive defensive secretion. This secretion is a flexible hydrogel that is toughened by a double network mechanism. While synthetic double network gels typically require extensive time to prepare, this slug creates a tough gel in seconds. To gain insight into how the glue forms a double-network hydrogel so rapidly, the secretory apparatus of this slug was analyzed. The goal was to determine how the major components of the glue were distributed and mixed. Most of the glue comes from two types of large unicellular glands; one secretes polyanionic polysaccharides in small, membrane-bound packets, the other secretes proteins that appear to form a cross-linked network. The latter gland shows distinct regions where cross-linking appears to be occurring. These regions are darker, more homogeneous and appear more solid than the rest of the secretory material. The enzyme catalase is highly abundant in these regions, as are basic proteins. These results suggest that a rapid oxidation event occurs in this protein-containing gland, triggering cross-linking before the glue is released. The cross-linked microgels would then join together after secretion to form a granular hydrogel. The polysaccharide-filled packets would be mixed and interspersed among these microgels and may contribute to joining them together. This is an unexpected and highly effective way to form a tough gel rapidly.
Funding text :
We would like to thank W. M. Kier for assistance with the semi-thin methacrylate sections. This work was supported by the Fonds de la Recherche Scientifique \u2013 FNRS under Grants EQP UN07220F and PDR T.0088.20, and by the Research Institute for Biosciences of the University of Mons (Action 5). P. F. is Research Director of the FRS-FNRS.
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