Abstract
Hirudin P6 is a leech-derived anti-thrombotic protein which possesses two post-translational modifications, O-glycosylation and tyrosine sulfation. In this study we report the ligation-based synthesis of a library of hirudin P6 proteins possessing homogeneous glycosylation and sulfation modifications. The nature of the modifications incorporated was shown to have a drastic effect on inhibition against both the fibrinogenolytic and amidolytic activities of thrombin and thus highlights a potential means for attenuating the biological activity of the protein.
| Original language | English |
|---|---|
| Pages (from-to) | 3947-3951 |
| Journal | Angewandte Chemie (International Edition) |
| Volume | 53 |
| Issue number | 15 |
| DOIs | |
| Publication status | Published - 31 Dec 2014 |
Keywords
- Biologically Active Molecules
- Organic Chemical Synthesis
- Proteins and Peptides
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