Engineering sulfotransferases to modify heparan sulfate

Nat Chem Biol. 2008 Mar;4(3):200-2. doi: 10.1038/nchembio.66. Epub 2008 Jan 27.

Abstract

The biosynthesis of heparan sulfate (HS) involves an array of specialized sulfotransferases. Here, we present a study aimed at engineering the substrate specificity of different HS 3-O-sulfotransferase isoforms. Based on the crystal structures, we identified a pair of amino acid residues responsible for selecting the substrates. Mutations of these residues altered the substrate specificities. Our results demonstrate the feasibility of tailoring the specificity of sulfotransferases to modify HS with desired functions.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Carbohydrate Conformation
  • Feasibility Studies
  • Heparitin Sulfate / biosynthesis*
  • Heparitin Sulfate / chemistry
  • Models, Molecular
  • Mutagenesis, Site-Directed
  • Protein Engineering*
  • Protein Isoforms / chemistry
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism*
  • Substrate Specificity
  • Sulfotransferases / chemistry
  • Sulfotransferases / genetics
  • Sulfotransferases / metabolism*

Substances

  • Protein Isoforms
  • Heparitin Sulfate
  • Sulfotransferases
  • heparan sulfate D-glucosaminyl 3-O-sulfotransferase

Associated data

  • PubChem-Substance/46499873
  • PubChem-Substance/46499874
  • PubChem-Substance/46499875
  • PubChem-Substance/46499876
  • PubChem-Substance/46499877
  • PubChem-Substance/46499878