DiaPharma α-Thrombin Purified Enzyme, Human (100µg)
$0.00
Proteolytic Activation of Prothrombin
The serine protease α-thrombin is produced by proteolytic activation of the zymogen, prothrombin. The enzyme complex, prothrombinase, catalyzes the proteolysis of two peptide bonds in prothrombin, which gives rise to an NH2-terminal derived
Properties of Thrombin
| Localization: | Plasma | ||||||||
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| Mode of action: | Serine protease which cleaves fibrinogen to form fibrin; also responsible for activation of protein C, platelet activation and feedback activation of the procofactors, factor V and factor VIII | ||||||||
| Molecular weight: | 36,700 | ||||||||
| Extinction coefficient: |
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| Specific Activity: | approximately 3800 NIH units/mg | ||||||||
| Isoelectric point: | 7.0-7.6 (human) | ||||||||
| Structure: | two subunits, approximately Mr=6,000 and 31,000 | ||||||||
| Percent carbohydrate: | approximately 5% |
Images
Formulation
50% glycerol/water (v/v)
Purity
>95% by SDS-PAGE
NOT tissue/cell culture grade. Not tested for endotoxin.
Activity
Fibrinogen clotting or chromogenic assay
Storage & Stability
| Storage | Glyercol formulation: -20°C |
|---|---|
| Shelf Life (Properly Stored) | 12 months |
Sample Gel Info
| Gel | Novex 4-12% Bis-Tris |
|---|---|
| Load | Human Thrombin, 1 µg per lane |
| Buffer | MES |
| Standard | SeeBluePlus 2; Myosin (188 kDa), Phosphorylase B (98 kDa), BSA (62 kDa), Glutamic Dehydrogenase (49 kDa), Alcohol Dehydrogenase (38 kDa), Carbonic Anhydrase (28 kDa), Myoglobin Red (17 kDa), Lysozyme (14 kDa), Aprotinin (6 kDa), Insulin, B chain (3 kDa). |
Background
Overview of Thrombin
Alpha-thrombin is a highly specific serine protease generated by proteolytic activation of the zymogen prothrombin. During coagulation, thrombin cleaves fibrinogen to form fibrin, leading to the ultimate step in coagulation, the formation of a fibrin clot. Thrombin is also responsible for feedback activation of the procofactors factor V and factor VIII. Thrombin has also been reported to activate factor XIII and platelets, and also functions as a vasoconstrictor protein. The procoagulant activity of thrombin is arrested in two ways:
- inhibition by either heparin cofactor II or the antithrombin III/heparin complex; or
- complex formation with thrombomodulin. Formation of the thrombin/thrombomodulin complex results in the inability of thrombin to cleave fibrinogen and activate factors V and VIII, but increases the efficiency of thrombin for activation of the anticoagulant, protein C.
Thrombin is a two chain enzyme composed of an NH2-terminal “A” chain (Mr=6,000) and a COOH-terminal “B” chain (Mr=31,000) which remain covalently associated through a single disulfide bond. Human thrombin is 13 amino acids shorter than the bovine thrombin due to a thrombin cleavage site on the human protein that is not present in the bovine protein.
Thrombin is also utilized for site specific cleavage of fusion proteins expressed in bacteria. A thrombin sensitive site is incorporated between the recombinant protein of interest and peptides or proteins which facilitate purification and/or expression. The target protein is released from the expressed hybrid by cleavage with thrombin. Thrombin can then be easily removed by affinity chromatography.
Human, bovine and mouse thrombin are prepared from purified prothrombin using a modification of the Lundblad procedure as described by Nesheim et al. Thrombin is supplied in 50% (vol/vol) glycerol/H2O and should be stored at -20°C. Purity is determined by SDS-PAGE analysis and activity is measured in a thrombin specific clotting assay, and compared to standardized NIH thrombin. Thrombin is also available with the active site blocked with either DFP, FPRck, or biotinlyated FPRck.
Cleavage of Fusion Proteins
In addition to its broad application in coagulation research thrombin can be used for site specific cleavage of fusion proteins. A thrombin sensitive site is incorporated between the recombinant protein of interest and peptides or proteins which facilitate purification and/or expression. The target protein is released from the expressed hybrid by cleavage with thrombin. Thrombin can then be easily removed by affinity chromatography. Lot to lot consistency ensures reproducible results every time. For experiments involving cell cultures, please contact us to discuss custom, low endotoxin lots designated for cell culture use.