Photoactivatable Mussel-Based Underwater Adhesive Proteins by an Expanded Genetic Code

Chembiochem. 2017 Sep 19;18(18):1819-1823. doi: 10.1002/cbic.201700327. Epub 2017 Aug 1.

Abstract

Marine mussels exhibit potent underwater adhesion abilities under hostile conditions by employing 3,4-dihydroxyphenylalanine (DOPA)-rich mussel adhesive proteins (MAPs). However, their recombinant production is a major biotechnological challenge. Herein, a novel strategy based on genetic code expansion has been developed by engineering efficient aminoacyl-transfer RNA synthetases (aaRSs) for the photocaged noncanonical amino acid ortho-nitrobenzyl DOPA (ONB-DOPA). The engineered ONB-DOPARS enables in vivo production of MAP type 5 site-specifically equipped with multiple instances of ONB-DOPA to yield photocaged, spatiotemporally controlled underwater adhesives. Upon exposure to UV light, these proteins feature elevated wet adhesion properties. This concept offers new perspectives for the production of recombinant bioadhesives.

Keywords: biomimetic synthesis; computational chemistry; mussel adhesive protein; photochemistry; scanning probe microscopy; synthetases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adhesives / radiation effects
  • Amino Acyl-tRNA Synthetases / metabolism
  • Animals
  • Biomimetic Materials / metabolism
  • Bivalvia / genetics
  • Bivalvia / metabolism*
  • Dihydroxyphenylalanine / metabolism
  • Genetic Code / genetics*
  • Microscopy, Atomic Force
  • Microscopy, Scanning Probe
  • Mutagenesis, Site-Directed
  • Proteins / genetics
  • Proteins / metabolism*
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / isolation & purification
  • Ultraviolet Rays

Substances

  • Adhesives
  • Proteins
  • Recombinant Proteins
  • adhesive protein, mussel
  • Dihydroxyphenylalanine
  • Amino Acyl-tRNA Synthetases