Identification and Mechanistic Analysis of a Novel Tick-Derived Inhibitor of Thrombin
Language English Country United States Media electronic-ecollection
Document type Journal Article, Research Support, N.I.H., Intramural, Research Support, Non-U.S. Gov't
Grant support
Intramural NIH HHS - United States
PubMed
26244557
PubMed Central
PMC4526366
DOI
10.1371/journal.pone.0133991
PII: PONE-D-15-21568
Knihovny.cz E-resources
- MeSH
- Platelet Aggregation drug effects MeSH
- Anticoagulants chemistry isolation & purification pharmacology MeSH
- Blood Coagulation drug effects MeSH
- Ticks chemistry MeSH
- Humans MeSH
- Molecular Sequence Data MeSH
- Mice, Inbred BALB C MeSH
- Mice MeSH
- Peptides chemistry isolation & purification pharmacology MeSH
- Amino Acid Sequence MeSH
- Sequence Alignment MeSH
- Thrombin antagonists & inhibitors metabolism MeSH
- Thrombosis drug therapy MeSH
- Blood Coagulation Tests MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Intramural MeSH
- Names of Substances
- Anticoagulants MeSH
- Peptides MeSH
- Thrombin MeSH
A group of peptides from the salivary gland of the tick Hyalomma marginatum rufipes, a vector of Crimean Congo hemorrhagic fever show weak similarity to the madanins, a group of thrombin-inhibitory peptides from a second tick species, Haemaphysalis longicornis. We have evaluated the anti-serine protease activity of one of these H. marginatum peptides that has been given the name hyalomin-1. Hyalomin-1 was found to be a selective inhibitor of thrombin, blocking coagulation of plasma and inhibiting S2238 hydrolysis in a competitive manner with an inhibition constant (Ki) of 12 nM at an ionic strength of 150 mM. It also blocks the thrombin-mediated activation of coagulation factor XI, thrombin-mediated platelet aggregation, and the activation of coagulation factor V by thrombin. Hyalomin-1 is cleaved at a canonical thrombin cleavage site but the cleaved products do not inhibit coagulation. However, the C-terminal cleavage product showed non-competitive inhibition of S2238 hydrolysis. A peptide combining the N-terminal parts of the molecule with the cleavage region did not interact strongly with thrombin, but a 24-residue fragment containing the cleavage region and the C-terminal fragment inhibited the enzyme in a competitive manner and also inhibited coagulation of plasma. These results suggest that the peptide acts by binding to the active site as well as exosite I or the autolysis loop of thrombin. Injection of 2.5 mg/kg of hyalomin-1 increased arterial occlusion time in a mouse model of thrombosis, suggesting this peptide could be a candidate for clinical use as an antithrombotic.
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