Platelet-decorated von Willebrand factor (VWF) strings anchored to the endothelial surface are rapidly cleaved by ADAMTS13. Individual VWF string characteristics such as number, location, and auxiliary features of the ADAMTS13 cleavage sites were explored here using imaging and computing software. By following changes in VWF string length, we demonstrated that VWF strings are cleaved multiple times, successively shortening string length in the function of time and generating fragments ranging in size from 5 to over 100 mu m. These are larger than generally observed in normal plasma, indicating that further proteolysis takes place in circulation. Interestingly, in 89% of all cleavage events, VWF strings elongate precisely at the cleavage sit...
Von Willebrand factor (VWF) is a key protein in hemostasis as it mediates adhesion of blood platelet...
ciently cleaves only the Tyr1605-Met1606 bond in the central A2 domain of multi-meric von Willebrand...
Platelet recruitment to sites of blood vessel damage is highly dependent upon von Willebrand factor ...
Platelet-decorated von Willebrand factor (VWF) strings anchored to the endothelial surface are rapid...
von Willebrand factor (VWF) is amongst others synthesized by endothelial cells and stored as ultra-l...
Background: The multidomain metalloprotease ADAMTS13 regulates the size of von Willebrand factor (VW...
von Willebrand factor (VWF) is a large adhesive glycoprotein with established functions in hemostasi...
Background and Objective: Von Willebrand factor (VWF) forms strings on activated vascular endothelia...
ADAMTS13 (A Disintegrin And Metalloprotease with ThromboSpondin type1 repeats-13) is an enzyme that ...
ADAMTS13 (A Disintegrin And Metalloprotease with ThromboSpondin type1 repeats-13) is an enzyme that ...
Endothelial cells secrete prothrombotic ul-tralarge von Willebrand factor (VWF) multim-ers, and the ...
von Willebrand factor (VWF) strings are removed from the endothelial surface by ADAMTS13 (a disinteg...
Von Willebrand factor (VWF) is a large, multimeric protein that regulates hemostasis by tethering pl...
Background: ADAMTS-13 proteolytic activity is controlled by the conformation of its substrate, von W...
The haemostatic potential of von Willebrand factor, a glycoprotein expressed by endothelial cells as...
Von Willebrand factor (VWF) is a key protein in hemostasis as it mediates adhesion of blood platelet...
ciently cleaves only the Tyr1605-Met1606 bond in the central A2 domain of multi-meric von Willebrand...
Platelet recruitment to sites of blood vessel damage is highly dependent upon von Willebrand factor ...
Platelet-decorated von Willebrand factor (VWF) strings anchored to the endothelial surface are rapid...
von Willebrand factor (VWF) is amongst others synthesized by endothelial cells and stored as ultra-l...
Background: The multidomain metalloprotease ADAMTS13 regulates the size of von Willebrand factor (VW...
von Willebrand factor (VWF) is a large adhesive glycoprotein with established functions in hemostasi...
Background and Objective: Von Willebrand factor (VWF) forms strings on activated vascular endothelia...
ADAMTS13 (A Disintegrin And Metalloprotease with ThromboSpondin type1 repeats-13) is an enzyme that ...
ADAMTS13 (A Disintegrin And Metalloprotease with ThromboSpondin type1 repeats-13) is an enzyme that ...
Endothelial cells secrete prothrombotic ul-tralarge von Willebrand factor (VWF) multim-ers, and the ...
von Willebrand factor (VWF) strings are removed from the endothelial surface by ADAMTS13 (a disinteg...
Von Willebrand factor (VWF) is a large, multimeric protein that regulates hemostasis by tethering pl...
Background: ADAMTS-13 proteolytic activity is controlled by the conformation of its substrate, von W...
The haemostatic potential of von Willebrand factor, a glycoprotein expressed by endothelial cells as...
Von Willebrand factor (VWF) is a key protein in hemostasis as it mediates adhesion of blood platelet...
ciently cleaves only the Tyr1605-Met1606 bond in the central A2 domain of multi-meric von Willebrand...
Platelet recruitment to sites of blood vessel damage is highly dependent upon von Willebrand factor ...