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 ItzsteinPublished 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.