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Functional and structural characterization of a heparanase.

Lisa BohlmannGregory D TredwellXing YuChih-Wei ChangThomas HaselhorstMoritz WingerJeffrey C DyasonRobin J ThomsonJoe TiralongoIfor R BeachamHelen BlanchardMark von Itzstein
Published in: Nature chemical biology (2015)
We report the structural and functional characterization of a novel heparanase (BpHep) from the invasive pathogenic bacterium Burkholderia pseudomallei (Bp), showing ∼24% sequence identity with human heparanase (hHep). Site-directed mutagenesis studies confirmed the active site resi-dues essential for activity, and we found that BpHep has specificity for heparan sulfate. Finally, we describe the first heparanase X-ray crystal structure, which provides new insight into both substrate recognition and inhibitor design.
Keyphrases
  • crystal structure
  • endothelial cells
  • crispr cas
  • high resolution
  • induced pluripotent stem cells
  • amino acid
  • computed tomography
  • structural basis