Home LiteratureArticle Details
PMID: 3485111 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Subunit composition of plasma von Willebrand factor. Cleavage is present in normal individuals, increased in IIA and IIB von Willebrand disease, but minimal in variants with aberrant structure of individual oligomers (types IIC, IID, and IIE).

The Journal of clinical investigation ·Vol. 77 ·No. 3 ·1986-03-00 ·Pages 947-51

Zimmerman TS, Dent JA, Ruggeri ZM, Nannini LH

Abstract

We have evaluated the subunit composition of plasma von Willebrand factor (vWF) and found evidence that cleavage is present in normal individuals, increased in IIA and IIB von Willebrand disease (vWD), but decreased or absent in variants with aberrant structure of individual oligomers. vWF was rapidly purified from plasma on an analytical scale by monoclonal antibody immunoaffinity chromatography in the presence of protease inhibitors. After reduction and electrophoresis in 5% polyacrylamide gels containing sodium dodecyl sulfate, fragments of 189, 176, and 140 kD, as well as the predominant 225-kD subunit, were identified in plasma vWF from 25 normal individuals. The vWF polypeptides were detected by immunoblotting with a mixture of 55 anti-vWF monoclonal antibodies followed by 125I-rabbit anti-mouse antibody and autoradiography. In five individuals with type IIA and five individuals with type IIB vWD, the proportions of 176 and 140-kD fragments were increased relative to the intact 225-kD subunit, as determined by excising each band and quantitating incorporated radioactivity. In contrast, these fragments were either not detectable or were present in only trace amounts in variants with abnormal structure of individual oligomers (types IIC and IID, and a new variant, type IIE vWD). The results reported here provide evidence that absence of large vWF multimers in these two groups of variants results from different mechanisms. In addition, they demonstrate that partial cleavage of the plasma vWF subunit is a normal event.

MeSH Terms
Antibodies, Monoclonal Humans Macromolecular Substances Molecular Weight Peptide Fragments/analysis von Willebrand Diseases/blood,classification,genetics von Willebrand Factor/genetics,metabolism
Chemicals
Antibodies, Monoclonal Macromolecular Substances Peptide Fragments von Willebrand Factor
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Zimmerman T S
Dent J A
Ruggeri Z M
Nannini L H
References (18)
18 references, click to expand
  1. Cleavage of structural proteins during the assembly of the head of bacteriophage T4.
    Nature. 1970 Aug 15;227(5259):680-5 PMID: 5432063
  2. von Willebrand disease type IIC with different abnormalities of von Willebrand factor in the same sibship.
    Am J Hematol. 1986 Feb;21(2):177-88 PMID: 3484608
  3. Heightened interaction between platelets and factor VIII/von Willebrand factor in a new subtype of von Willebrand's disease.
    N Engl J Med. 1980 May 8;302(19):1047-51 PMID: 6767976
  4. Variant von Willebrand's disease: characterization of two subtypes by analysis of multimeric composition of factor VIII/von Willebrand factor in plasma and platelets.
    J Clin Invest. 1980 Jun;65(6):1318-25 PMID: 6773982
  5. The complex multimeric composition of factor VIII/von Willebrand factor.
    Blood. 1981 Jun;57(6):1140-3 PMID: 6784794
  6. Properties of human asialo-factor VIII. A ristocetin-independent platelet-aggregating agent.
    J Clin Invest. 1981 Aug;68(2):321-8 PMID: 6790574
  7. Characterization of the human factor VIII procoagulant protein with a heterologous precipitating antibody.
    Proc Natl Acad Sci U S A. 1982 Mar;79(5):1648-52 PMID: 6803246
  8. Aberrant multimeric structure of von Willebrand factor in a new variant of von Willebrand's disease (type IIC).
    J Clin Invest. 1982 Nov;70(5):1124-7 PMID: 6982283
  9. Platelet aggregation induced by 1-desamino-8-D-arginine vasopressin (DDAVP) in Type IIB von Willebrand's disease.
    N Engl J Med. 1983 Oct 6;309(14):816-21 PMID: 6412139
  10. A variant of von Willebrand's disease characterized by recessive inheritance and missing triplet structure of von Willebrand factor multimers.
    Blood. 1983 Nov;62(5):1000-5 PMID: 6605165
  11. A new variant of dominant type II von Willebrand's disease with aberrant multimeric pattern of factor VIII-related antigen (type IID).
    Blood. 1984 Jun;63(6):1369-71 PMID: 6426551
  12. Cleavage of human von Willebrand factor by platelet calcium-activated protease.
    Blood. 1985 Feb;65(2):352-6 PMID: 2981585
  13. Type IIB Tampa: a variant of von Willebrand disease with chronic thrombocytopenia, circulating platelet aggregates, and spontaneous platelet aggregation.
    Blood. 1985 Aug;66(2):282-6 PMID: 3926021
  14. Effects of plasmin on von Willebrand factor multimers. Degradation in vitro and stimulation of release in vivo.
    J Clin Invest. 1985 Jul;76(1):261-70 PMID: 3160727
  15. In vitro correction of the abnormal multimeric structure of von Willebrand factor in type IIa von Willebrand's disease.
    Proc Natl Acad Sci U S A. 1985 Sep;82(17):5968-72 PMID: 2994057
  16. Interaction of purified type IIB von Willebrand factor with the platelet membrane glycoprotein Ib induces fibrinogen binding to the glycoprotein IIb/IIIa complex and initiates aggregation.
    Proc Natl Acad Sci U S A. 1985 Nov;82(21):7424-8 PMID: 2932740
  17. von Willebrand factor. A reduced and alkylated 52/48-kDa fragment beginning at amino acid residue 449 contains the domain interacting with platelet glycoprotein Ib.
    J Biol Chem. 1986 Jan 5;261(1):381-5 PMID: 2934387
  18. Enzymatic degradation of the factor-VIII-von-Willebrand protein: a unique tryptic fragment with ristocetin cofactor activity.
    Blood. 1980 May;55(5):848-58 PMID: 6767513
Article Info
Journal
The Journal of clinical investigation
Abbr.
J Clin Invest
ISSN
0021-9738
Published
1986-03-00
Pages
947-51
Language
English
Region
United States
NLM ID
7802877
PMCID
PMC423489
Subset
IM
Grants
NHLBI NIH HHS · HL15491 · United States
NHLBI NIH HHS · HL31950 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com