Localization of Phosphoproteins within the Barnacle Adhesive Interface.

Published

Journal Article

Barnacles permanently adhere to nearly any inert substrate using proteinaceous glue. The glue consists of at least ten major proteins, some of which have been isolated and sequenced. Questions still remain about the chemical mechanisms involved in adhesion and the potential of the glue to serve as a platform for mineralization of the calcified base plate. We tested the hypothesis that barnacle glue contains phosphoproteins, which have the potential to play a role in both adhesion and mineralization. Using a combination of phosphoprotein-specific gel staining and Western blotting with anti-phosphoserine antibody, we identified multiple phosphorylated proteins in uncured glue secretions from the barnacle Amphibalanus amphitrite The protein composition of the glue and the quantity and abundance of phosphoproteins varied distinctly among individual barnacles, possibly due to cyclical changes in the glue secretion over time. We assessed the location of the phosphoproteins within the barnacle glue layer using decalcified barnacle base plates and residual glue deposited by reattached barnacles. Phosphoproteins were found throughout the organic matrix of the base plate and within the residual glue. Staining within the residual glue appeared most intensely in regions where capillary glue ducts, which are involved in cyclical release of glue, had been laid down. Lastly, mineralization studies of glue proteins separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) indicated that proteins identified as phosphorylated possibly induce mineralization of calcium carbonate (CaCO3). These results contribute to our understanding of the protein composition of barnacle glue, and provide new insights into the potential roles of phosphoproteins in underwater bioadhesives.

Full Text

Duke Authors

Cited Authors

  • Dickinson, GH; Yang, X; Wu, F; Orihuela, B; Rittschof, D; Beniash, E

Published Date

  • June 2016

Published In

Volume / Issue

  • 230 / 3

Start / End Page

  • 233 - 242

PubMed ID

  • 27365418

Pubmed Central ID

  • 27365418

Electronic International Standard Serial Number (EISSN)

  • 1939-8697

International Standard Serial Number (ISSN)

  • 0006-3185

Digital Object Identifier (DOI)

  • 10.1086/BBLv230n3p233

Language

  • eng