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Partial purification and characterization of a protease from human plasma
cleaving von Willebrand factor to fragments produced by in vivo proteolysis
M Furlan, R Robles and B Lamie
Central Hematology Laboratory of the University, Inselspital, Bern,
Switzerland.
Proteolytic cleavage of von Willebrand factor (vWF) takes place in the
circulating blood of healthy subjects and is increased in some patients
with von Willebrand disease type 2A. The hemostatically active large vWF
multimers are degraded to smaller less active forms. It has been suggested
that the polypeptide subunit of vWF is cleaved at the peptide bond
842Tyr-843Met. We purified (approximately 10,000-fold) from human plasma a
vWF-degrading protease, using chelating Sepharose, hydrophobic interaction
chromatography, and gel filtration. The enzyme was found to be virtually
absent in the platelet lysates obtained by repeated freezing and thawing.
The proteolytic activity was associated with a high molecular weight
protein (approximately 300 kD) as judged by gel filtration and sodium
dodecyl sulfate-polyacrylamide gel electrophoresis. vWF was resistant
against the protease in a neutral buffer at physiological ionic strength
but became degraded at low salt concentration or in the presence of 1 mol/L
urea. No degradation of human fibrinogen, bovine serum albumin, of calf
skin collagen by the purified protease was noted under the same
experimental conditions. Proteolytic activity showed a pH optimum at 8 to 9
and was strongly inhibited by chelating agents, whereas only slow
inhibition was observed with N-ethylmaleimide. There was no inhibition by
iodoacetamide, leupeptin, or serine protease inhibitors. The best peptidyl
diazomethyl ketone inhibitor was Z-Phe-Phe-CHN2. Activation by divalent
metal ions was found to increase in the following order: Zn2+ approximately
Cu2+ approximately CD2+ approximately Ni2+ approximately Co2+ <Mn2+
<Mg2+ <Ca2+ <Sr2+ <Ba2+. The observed properties of the vWF-
degrading enzyme differ from those of all other hitherto described
proteases. Purified vWF was incubated with the protease, and the degraded
material subjected to sodium dodecyl sulfate-polyacrylamide gel
electrophoresis after disulfide reduction. The size, amino acid
composition, and amino terminal sequence of the reduced fragments confirmed
that the peptide bond 842Tyr-843Met had been cleaved, ie, the same bond
that has been proposed to be cleaved in vivo.
Volume 87,
Issue 10,
pp. 4223-4234,
05/15/1996
Copyright © 1996 by The American Society of Hematology

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K. Kokame, M. Matsumoto, Y. Fujimura, and T. Miyata
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J. E. Pimanda, A. Maekawa, T. Wind, J. Paxton, C. N. Chesterman, and P. J. Hogg
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J. E. Sadler, J. L. Moake, T. Miyata, and J. N. George
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J. Caprioli, F. Castelletti, S. Bucchioni, P. Bettinaglio, E. Bresin, G. Pianetti, S. Gamba, S. Brioschi, E. Daina, G. Remuzzi, et al.
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E. M. Majerus, X. Zheng, E. A. Tuley, and J. E. Sadler
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K. Soejima, M. Matsumoto, K. Kokame, H. Yagi, H. Ishizashi, H. Maeda, C. Nozaki, T. Miyata, Y. Fujimura, and T. Nakagaki
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F. Scheiflinger, P. Knobl, B. Trattner, B. Plaimauer, G. Mohr, M. Dockal, F. Dorner, and M. Rieger
Nonneutralizing IgM and IgG antibodies to von Willebrand factor-cleaving protease (ADAMTS-13) in a patient with thrombotic thrombocytopenic purpura
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J.-f. Dong, J. L. Moake, A. Bernardo, K. Fujikawa, C. Ball, L. Nolasco, J. A. Lopez, and M. A. Cruz
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X. Zheng, K. Nishio, E. M. Majerus, and J. E. Sadler
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H.-M. Tsai
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H.-M. Tsai
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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.
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J.-f. Dong, J. L. Moake, L. Nolasco, A. Bernardo, W. Arceneaux, C. N. Shrimpton, A. J. Schade, L. V. McIntire, K. Fujikawa, and J. A. Lopez
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H.-M. Tsai, B. Lammle, V. Bianchi, L. Alberio, M. Furlan, G. Remuzzi, M. Galbusera, and P. M. Mannucci
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J. E. Sadler
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J. L. Moake
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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.
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V. Bianchi, R. Robles, L. Alberio, M. Furlan, and B. Lammle
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T. J. Raife, S. R. Lentz, B. S. Atkinson, S. K. Vesely, and M. J. Hessner
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J. N. George, J. E. Sadler, and B. Lammle
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P. M. Mannucci, M. T. Canciani, I. Forza, F. Lussana, A. Lattuada, and E. Rossi
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H. E. Gerritsen, R. Robles, B. Lammle, and M. Furlan
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K. Fujikawa, H. Suzuki, B. McMullen, and D. Chung
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A. Veyradier, B. Obert, A. Houllier, D. Meyer, and J.-P. Girma
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J. C. Moore, C. P. M. Hayward, T. E. Warkentin, and J. G. Kelton
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K. Spring, S. Cross, C. Li, D. Watters, L. Ben-Senior, P. Waring, F. Ahangari, S.-l. Lu, P. Chen, I. Misko, et al.
Atm Knock-in Mice Harboring an In-frame Deletion Corresponding to the Human ATM 7636del9 Common Mutation Exhibit a Variant Phenotype
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R. Schneppenheim, U. Budde, T. Obser, J. Brassard, K. Mainusch, Z. M. Ruggeri, S. Schneppenheim, R. Schwaab, and J. Oldenburg
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C. V. Denis, K. Kwack, S. Saffaripour, S. Maganti, P. Andre, R. G. Schaub, and D. D. Wagner
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K. R. McCrae, J. B. Bussel, P. M. Mannucci, G. Remuzzi, and D. B. Cines
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F. I. Pareti, A. Lattuada, C. Bressi, M. Zanobini, A. Sala, A. Steffan, and Z. M. Ruggeri
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M. Furlan and B. Lammle
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