• metalloendopeptidase activity • integrin binding • calcium ion binding • protein binding • peptidase activity • zinc ion binding
• proteinaceous extracellular matrix • extracellular space • cell surface
• proteolysis • cell-matrix adhesion • integrin-mediated signaling pathway • glycoprotein metabolic process • protein processing • platelet activation • peptide catabolic process
RNA expression pattern
More reference expression data
NM_139028 (mRNA) NP_620597 (protein)
XM_914175 (mRNA) XP_919268 (protein)
Chr 9: 135.28 - 135.31 Mb
ADAMTS13 (A Disintegrin And Metalloproteinase with a ThromboSpondin type 1 motif, member 13) is a zinc-containing metalloprotease enzyme that cleaves von Willebrand factor (vWf), a large protein involved in blood clotting. It is also known as von Willebrand factor-cleaving protease (VWFCP). It is secreted in blood and degrades large vWf multimers, decreasing their activity.
The ADAMTS13 gene maps to the ninth chromosome (9q34).
Discovery and function
Since 1982 it had been known that thrombotic thrombocytopenic purpura (TTP), one of the microangiopathic hemolytic anemias (see below), was characterised in its familial form by the presence in plasma of unusually large von Willebrand factor multimers (ULVWF).
In 1994, VWF was shown to be cleaved between a tyrosine at position 1605 and a methionine at 1606 by a plasma metalloprotease when it was exposed to high levels of shear stress. In 1996, two research groups independently further characterized the enzyme that cleaved VWF. In the next two years, the same two groups showed that the congenital deficiency of vWf-cleaving protease was associated with formation of platelet microthrombi in the small blood vessels. In addition, they reported that in majority of patients IgGantibodies, directed against this enzyme, caused TTP in non-familial cases.
Genomically, ADAMTS13 shares many properties with the 19 member ADAMTS family, all of which are characterised by a protease domain (the part that performs the protein hydrolysis), an adjacent disintegrin domain and one or more thrombospondin domains. ADAMTS13 in fact has eight thrombospondin domains. It has no hydrophobic transmembrane domain, and hence it not anchored in the cell membrane.
Role in disease
Deficiency of ADAMTS13 was originally discovered in Upshaw-Shulman syndrome, the recurring familial form of TTP. By that time it was already suspected that TTP occurred in the autoimmune form as well, owing to its response to plasmapheresis and characterisation of IgG inhibitors. Since the discovery of ADAMTS13, specific epitopes on its surface have been shown to be the target of inhibitory antibodies.
Especially since the link between aortic valve stenosis and angiodysplasia was proven to be due to high shear stress (Heyde's syndrome), it has been accepted that increased exposure of vWf to ADAMTS13 due to various reasons would predispose to bleeding by causing increased degradation of vWf. This phenomenon is characterised by a form of von Willebrand disease (type 2a).
^ abcdefg Levy GG, Motto DG, Ginsburg D (2005). "ADAMTS13 turns 3". Blood106 (1): 11–7. doi:10.1182/blood-2004-10-4097. PMID 15774620.
^ Tsai HM (2003). "Advances in the pathogenesis, diagnosis, and treatment of thrombotic thrombocytopenic purpura". J. Am. Soc. Nephrol.14 (4): 1072–81. PMID 12660343.
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