Incorporation of glycosylated amino acid into protein by an in vitro translation system

Bioorg Med Chem Lett. 2013 Oct 15;23(20):5634-6. doi: 10.1016/j.bmcl.2013.08.035. Epub 2013 Aug 15.

Abstract

O-GalNAcα-modified proteins are the precursor of mucin-type O-glycosylated proteins. Homogeneously O-glycosylated proteins are required to investigate the biological functions of glycoproteins and to develop biopharmaceuticals. Here we show that the incorporation of GalNAcα-Thr into proteins successfully proceeded by the use of a chemically aminoacylated tRNA. GalNAcα-Thr was chemoenzymatically attached to amber suppressor tRNA and the product was subjected to in vitro translation together with streptavidin mRNA containing the UAG codon. Gel electrophoresis and mass analysis showed that GalNAcα-Thr was successfully incorporated into the N-terminus, although it was not incorporated at the interior. This method will facilitate the preparation of homogeneous GalNAcα-proteins.

Keywords: Expanding genetic code; Glycoprotein; Glycosylated amino acid; In vitro translation system; O-Glycan.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylgalactosamine / metabolism*
  • Amino Acids / chemistry
  • Amino Acids / metabolism*
  • Codon, Terminator
  • Escherichia coli / metabolism
  • Glycosylation
  • Protein Biosynthesis
  • RNA, Transfer / metabolism
  • Streptavidin / chemistry
  • Streptavidin / genetics
  • Streptavidin / metabolism*

Substances

  • Amino Acids
  • Codon, Terminator
  • Streptavidin
  • RNA, Transfer
  • Acetylgalactosamine