Premium
Significance of the conformation of building blocks in curing of barnacle underwater adhesive
Author(s) -
Kamino Kei,
Nakano Masahiro,
Kanai Satoru
Publication year - 2012
Publication title -
the febs journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 204
eISSN - 1742-4658
pISSN - 1742-464X
DOI - 10.1111/j.1742-4658.2012.08552.x
Subject(s) - adhesive , biophysics , proteolysis , materials science , covalent bond , curing (chemistry) , intermolecular force , chemistry , polymer chemistry , nanotechnology , molecule , biochemistry , biology , organic chemistry , enzyme , layer (electronics)
Barnacles are a unique sessile crustacean that attach irreversibly and firmly to foreign underwater surfaces. Its biological underwater adhesive is a peculiar extracellular multi‐protein complex. Here we characterize one of the two major proteins, a 52 kDa protein found in the barnacle cement complex. Cloning of the cDNA revealed that the protein has no homolog in the nonredundant database. The primary structure consists of four long sequence repeats. The process of dissolving the protein at the adhesive joint of the animal by various treatments was monitored in order to obtain insight into the molecular mechanism involved in curing of the adhesive bulk. Treatments with protein denaturant, reducing agents and/or chemical‐specific proteolysis in combination with 2D diagonal PAGE indicated no involvement of the protein in intermolecular cross‐linkage/polymerization, including formation of intermolecular disulfide bonds. As solubilization of the proteins required high concentrations of denaturing agents, it appears that both the conformation of the protein as building blocks and non‐covalent molecular interactions between the building blocks, possibly hydrophobic interactions and hydrogen bonds, are crucial for curing of the cement. It was also suggested that the protein contributes to surface coupling by an anchoring effect to micro‐ to nanoscopic roughness of surfaces. Database
Sequence of Megabalanus rosa cp52k mRNA for 52 kDa cement protein has been submitted to the DNA Data Bank of Japan under accession number AB623048 .