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Physiologic cleavage of von Willebrand factor by a plasma protease is
dependent on its conformation and requires calcium ion
HM Tsai
Division of Hematology, Montefiore Medical Center, Bronx, NY 10467, USA.
von Willebrand factor (vWF) in the circulation is subjected to proteolysis.
In a recent study, we reported that normal plasma contains a protease
activity that cleaves vWF in a shear-dependent manner, causing a decrease
in its multimer size while generating dimers of the 140-kD and the 176-kD
fragments indistinguishable from those found in normal plasma. In this
study, the plasma protease has been partially purified and characterized
and the role of vWF conformation in its cleavage by the protease has been
further investigated. Guanidine HCl caused unfolding of vWF in a
concentration-dependent manner, resulting in a shift in its fluorescence
emission maxima to longer wavelengths. A dramatic increase in its
proteolytic susceptibility was seen at 1.1 to 1.2 mol/L guanidine HCl, a
concentration causing only a 3- to 4-nm shift in vWF emission maxima.
Although vWF molecules refolded as guanidine HCl was removed by dialysis,
the refolding was accompanied only by a partial recovery of the proteolytic
resistance. The plasma protease, partially purified by approximately 900
folds by Sephacryl S- 300 HR gel filtration, Matrex gel orange A dye
affinity chromatography, and Q Sepharose anion exchange, had a molecular
mass of approximately 200 kD and was inhibited by EDTA, EGTA, or
1,10-phenanthroline. The inhibition by EGTA or EDTA could be reversed by
Ca2+ but not by mg2+. It was not inhibited by a panel of synthetic and
natural protease inhibitors or adsorbed by gelatin-agarose, and it was
present in plasmas deficient in proteins involved in coagulation and
anticoagulation. The vWF fragments generated by the protease, as mapped by
peptide-specific antibodies VP-1 and LJ-7745, were in distinguishable from
the natural fragments but distinct from those produced by plasmin. High
molecular weight endothelial vWF, after exposure to guanidine HCLI or high
shear stress, was cleaved by the protease to smaller forms. These results
support the model that endothelial secreted vWF is converted to multimers
by a novel plasma metalloproteinase. Although native vWF exists in a
conformation relatively resistant to cleavage, an alteration in the
conformation by shear stress can lead to enhanced proteolytic
susceptibility. This model may explain the decrease in vWF multimer sizes
in various clinical conditions.
Volume 87,
Issue 10,
pp. 4235-4244,
05/15/1996
Copyright © 1996 by The American Society of Hematology

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|
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|
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|
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|
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|
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|
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|
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|

|
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|
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|
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|
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|
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|
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|

|
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|
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|
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|
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|
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[Abstract]
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|
 |
|

|
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|
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[Full Text]
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|
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|
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|
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H.-M. Tsai
Advances in the Pathogenesis, Diagnosis, and Treatment of Thrombotic Thrombocytopenic Purpura
J. Am. Soc. Nephrol.,
April 1, 2003;
14(4):
1072 - 1081.
[Abstract]
[Full Text]
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H.-M. Tsai
Platelet Activation and the Formation of the Platelet Plug: Deficiency of ADAMTS13 Causes Thrombotic Thrombocytopenic Purpura
Arterioscler Thromb Vasc Biol,
March 1, 2003;
23(3):
388 - 396.
[Abstract]
[Full Text]
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R. Schneppenheim, U. Budde, F. Oyen, D. Angerhaus, V. Aumann, E. Drewke, W. Hassenpflug, J. Haberle, K. Kentouche, E. Kohne, et al.
von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP
Blood,
March 1, 2003;
101(5):
1845 - 1850.
[Abstract]
[Full Text]
[PDF]
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H.-M. Tsai, B. Lammle, V. Bianchi, L. Alberio, M. Furlan, G. Remuzzi, M. Galbusera, and P. M. Mannucci
Deficiency of ADAMTS13 and thrombotic thrombocytopenic purpura
Blood,
November 15, 2002;
100(10):
3839 - 3842.
[Full Text]
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B. Plaimauer, K. Zimmermann, D. Volkel, G. Antoine, R. Kerschbaumer, P. Jenab, M. Furlan, H. Gerritsen, B. Lammle, H. P. Schwarz, et al.
Cloning, expression, and functional characterization of the von Willebrand factor-cleaving protease (ADAMTS13)
Blood,
November 15, 2002;
100(10):
3626 - 3632.
[Abstract]
[Full Text]
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J. E. Sadler
A new name in thrombosis, ADAMTS13
PNAS,
September 3, 2002;
99(18):
11552 - 11554.
[Full Text]
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K. Kokame, M. Matsumoto, K. Soejima, H. Yagi, H. Ishizashi, M. Funato, H. Tamai, M. Konno, K. Kamide, Y. Kawano, et al.
Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity
PNAS,
September 3, 2002;
99(18):
11902 - 11907.
[Abstract]
[Full Text]
[PDF]
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J. L. Moake
Thrombotic Microangiopathies
N. Engl. J. Med.,
August 22, 2002;
347(8):
589 - 600.
[Full Text]
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G. Remuzzi, M. Galbusera, M. Noris, M. T. Canciani, E. Daina, E. Bresin, S. Contaretti, J. Caprioli, S. Gamba, P. Ruggenenti, et al.
von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome
Blood,
July 18, 2002;
100(3):
778 - 785.
[Abstract]
[Full Text]
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V. Bianchi, R. Robles, L. Alberio, M. Furlan, and B. Lammle
Von Willebrand factor-cleaving protease (ADAMTS13) in thrombocytopenic disorders: a severely deficient activity is specific for thrombotic thrombocytopenic purpura
Blood,
June 28, 2002;
100(2):
710 - 713.
[Abstract]
[Full Text]
[PDF]
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J. N. George, J. E. Sadler, and B. Lammle
Platelets: Thrombotic Thrombocytopenic Purpura
Hematology,
January 1, 2002;
2002(1):
315 - 334.
[Abstract]
[Full Text]
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P. M. Mannucci, M. T. Canciani, I. Forza, F. Lussana, A. Lattuada, and E. Rossi
Changes in health and disease of the metalloprotease that cleaves von Willebrand factor
Blood,
November 1, 2001;
98(9):
2730 - 2735.
[Abstract]
[Full Text]
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H. E. Gerritsen, R. Robles, B. Lammle, and M. Furlan
Partial amino acid sequence of purified von Willebrand factor-cleaving protease
Blood,
September 15, 2001;
98(6):
1654 - 1661.
[Abstract]
[Full Text]
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K. Fujikawa, H. Suzuki, B. McMullen, and D. Chung
Purification of human von Willebrand factor-cleaving protease and its identification as a new member of the metalloproteinase family
Blood,
September 15, 2001;
98(6):
1662 - 1666.
[Abstract]
[Full Text]
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A. Veyradier, B. Obert, A. Houllier, D. Meyer, and J.-P. Girma
Specific von Willebrand factor-cleaving protease in thrombotic microangiopathies: a study of 111 cases
Blood,
September 15, 2001;
98(6):
1765 - 1772.
[Abstract]
[Full Text]
[PDF]
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J. C. Moore, C. P. M. Hayward, T. E. Warkentin, and J. G. Kelton
Decreased von Willebrand factor protease activity associated with thrombocytopenic disorders
Blood,
September 15, 2001;
98(6):
1842 - 1846.
[Abstract]
[Full Text]
[PDF]
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K. R. McCrae, J. B. Bussel, P. M. Mannucci, G. Remuzzi, and D. B. Cines
Platelets: An Update on Diagnosis and Management of Thrombocytopenic Disorders
Hematology,
January 1, 2001;
2001(1):
282 - 305.
[Abstract]
[Full Text]
[PDF]
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N. Mistry, S. L. Cranmer, Y. Yuan, P. Mangin, S. M. Dopheide, I. Harper, S. Giuliano, D. E. Dunstan, F. Lanza, H. H. Salem, et al.
Cytoskeletal regulation of the platelet glycoprotein Ib/V/IX-von Willebrand factor interaction
Blood,
November 15, 2000;
96(10):
3480 - 3489.
[Abstract]
[Full Text]
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F. I. Pareti, A. Lattuada, C. Bressi, M. Zanobini, A. Sala, A. Steffan, and Z. M. Ruggeri
Proteolysis of von Willebrand Factor and Shear Stress-Induced Platelet Aggregation in Patients With Aortic Valve Stenosis
Circulation,
September 12, 2000;
102(11):
1290 - 1295.
[Abstract]
[Full Text]
[PDF]
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M. Furlan and B. Lammle
Haemolytic-uraemic syndrome and thrombotic thrombocytopenic purpura--new insights into underlying biochemical mechanisms
Nephrol. Dial. Transplant.,
August 1, 2000;
15(8):
1112 - 1114.
[Full Text]
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S L Allford and S J Machin
Current understanding of the pathophysiology of thrombotic thrombocytopenic purpura
J. Clin. Pathol.,
July 1, 2000;
53(7):
497 - 501.
[Full Text]
[PDF]
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H.-M. Tsai, L. Rice, R. Sarode, T. W. Chow, and J. L. Moake
Antibody Inhibitors to von Willebrand Factor Metalloproteinase and Increased Binding of von Willebrand Factor to Platelets in Ticlopidine-Associated Thrombotic Thrombocytopenic Purpura
Ann Intern Med,
May 16, 2000;
132(10):
794 - 799.
[Abstract]
[Full Text]
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A. Nandi, P. Estess, and M. H. Siegelman
Hyaluronan Anchoring and Regulation on the Surface of Vascular Endothelial Cells Is Mediated through the Functionally Active Form of CD44
J. Biol. Chem.,
May 12, 2000;
275(20):
14939 - 14948.
[Abstract]
[Full Text]
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P.L. Turecek, L. Pichler, W. Auer, G. Eder, K. Varadi, A. Mitterer, W. Mundt, U. Schlokat, F. Dorner, L.O. Drouet, et al.
Evidence for Extracellular Processing of Pro-von Willebrand Factor After Infusion in Animals With and Without Severe von Willebrand Disease
Blood,
September 1, 1999;
94(5):
1637 - 1647.
[Abstract]
[Full Text]
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L. Oleksowicz, N. Bhagwati, and M. DeLeon-Fernandez
Deficient Activity of von Willebrand's Factor-cleaving Protease in Patients with Disseminated Malignancies
Cancer Res.,
May 1, 1999;
59(9):
2244 - 2250.
[Abstract]
[Full Text]
[PDF]
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M. Furlan, R. Robles, M. Galbusera, G. Remuzzi, P. A. Kyrle, B. Brenner, M. Krause, I. Scharrer, V. Aumann, U. Mittler, et al.
von Willebrand Factor-Cleaving Protease in Thrombotic Thrombocytopenic Purpura and the Hemolytic-Uremic Syndrome
N. Engl. J. Med.,
November 26, 1998;
339(22):
1578 - 1584.
[Abstract]
[Full Text]
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H.-M. Tsai and E. C.-Y. Lian
Antibodies to von Willebrand Factor-Cleaving Protease in Acute Thrombotic Thrombocytopenic Purpura
N. Engl. J. Med.,
November 26, 1998;
339(22):
1585 - 1594.
[Abstract]
[Full Text]
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J. L. Moake
Moschcowitz, Multimers, and Metalloprotease
N. Engl. J. Med.,
November 26, 1998;
339(22):
1629 - 1631.
[Full Text]
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M. Furlan, R. Robles, M. Solenthaler, and B. Lammle
Acquired Deficiency of von Willebrand Factor-Cleaving Protease in a Patient With Thrombotic Thrombocytopenic Purpura
Blood,
April 15, 1998;
91(8):
2839 - 2846.
[Abstract]
[Full Text]
[PDF]
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P. V. Jenkins, K. J. Pasi, and S. J. Perkins
Molecular Modeling of Ligand and Mutation Sites of the Type A Domains of Human von Willebrand Factor and Their Relevance to von Willebrand's Disease
Blood,
March 15, 1998;
91(6):
2032 - 2044.
[Abstract]
[Full Text]
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P. L. Turecek, H. Gritsch, L. Pichler, W. Auer, B. Fischer, A. Mitterer, W. Mundt, U. Schlokat, F. Dorner, H. J. M. Brinkman, et al.
In Vivo Characterization of Recombinant von Willebrand Factor in Dogs With von Willebrand Disease
Blood,
November 1, 1997;
90(9):
3555 - 3567.
[Abstract]
[Full Text]
[PDF]
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M. Furlan, R. Robles, M. Solenthaler, M. Wassmer, P. Sandoz, and B. Lammle
Deficient Activity of von Willebrand Factor-Cleaving Protease in Chronic Relapsing Thrombotic Thrombocytopenic Purpura
Blood,
May 1, 1997;
89(9):
3097 - 3103.
[Abstract]
[Full Text]
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H.-M. Tsai, I. I. Sussman, D. Ginsburg, H. Lankhof, J. J. Sixma, and R. L. Nagel
Proteolytic Cleavage of Recombinant Type 2A von Willebrand Factor Mutants R834W and R834Q: Inhibition by Doxycycline and by Monoclonal Antibody VP-1
Blood,
March 15, 1997;
89(6):
1954 - 1962.
[Abstract]
[Full Text]
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X. Zheng, D. Chung, T. K. Takayama, E. M. Majerus, J. E. Sadler, and K. Fujikawa
Structure of von Willebrand Factor-cleaving Protease (ADAMTS13), a Metalloprotease Involved in Thrombotic Thrombocytopenic Purpura
J. Biol. Chem.,
October 26, 2001;
276(44):
41059 - 41063.
[Abstract]
[Full Text]
[PDF]
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