Analysis of von Willebrand Factor Multimers by Simultaneous High- and Low-Resolution Vertical SDS-Agarose Gel Electrophoresis and Cy5-Labeled Antibody High-Sensitivity Fluorescence Detection

被引:26
作者
Ott, Helmut W. [1 ]
Griesmacher, Andrea [1 ]
Schnapka-Koepf, Mirjam [1 ]
Golderer, Georg [2 ]
Sieberer, Andrea [3 ]
Spannagl, Michael [4 ]
Scheibe, Burghardt [5 ]
Perkhofer, Susanne [1 ]
Will, Kerstin [6 ]
Budde, Ulrich [6 ]
机构
[1] Med Univ Innsbruck, A-6020 Innsbruck, Austria
[2] Univ Innsbruck, Bioctr, A-6020 Innsbruck, Austria
[3] Biomed Res Ctr, Orth, Austria
[4] Univ Munich, Med Clin, Munich, Germany
[5] GE Healthcare Europe, Vienna, Austria
[6] Aesculap Lab, Hamburg, Germany
关键词
von Willebrand factor multimers; Sodium dodecyl sulfate-agarose gel electrophoresis; Fluorescence detection; von Willebrand disease; VONWILLEBRAND-FACTOR MULTIMERS; ADAMTS13; DEFICIENCY; DISEASE; CLASSIFICATION; VISUALIZATION; LUMINOGRAPHY; ASSAY;
D O I
10.1309/AJCPZSBTD2BWOMVL
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Analysis of von Willebrand factor (vWF) multimers allows classification of the subtypes of von Willebrand disease (vWD) in human serum and platelet lysates. A novel method for multimer analysis of vWF by 2-chamber, vertical (sodium dodecyl sulfate), agarose gel electrophoresis, designed for comparing discontinuous high- and low-resolving gels for plasma and platelets, followed by Western blotting and high-sensitivity fluorescence detection (HSFD) of cyanine (Cy)5-labeled vWF multimers is presented. HSFD shows that this method has high discriminatory power for visualization and densitometric analysis of platelets and plasma vWF multimers in various types of vWD and allows rapid classification of vWD types, to separate types 2A and 2B. The described procedures of vWF multimer analysis with high-sensitivity Cy5 fluorescence detection and direct comparison of high- and low-resolving gels for screening and detection of the complete range of high- and low-molecular vWF multimers is efficient and useful for screening, detecting, and classifying vWD subtypes and makes this method diagnostically and clinically relevant.
引用
收藏
页码:322 / 330
页数:9
相关论文
共 25 条
[1]  
AIHARA M, 1986, THROMB HAEMOSTASIS, V55, P263
[2]  
BUDDE U, 1990, THROMB HAEMOSTASIS, V63, P312
[3]   Laboratory testing for von Willebrand Disease: Contribution of multimer analysis to diagnosis and classification [J].
Budde, Ulrich ;
Pieconka, Antje ;
Will, Kirsten ;
Schneppenheim, Reinhard .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2006, 32 (05) :514-521
[4]   Factor VIII accelerates proteolytic cleavage of von Willebrand factor by ADAMTS13 [J].
Cao, Wenjing ;
Krishnaswamy, Sriram ;
Camire, Rodney M. ;
Lenting, Peter J. ;
Zheng, X. Long .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (21) :7416-7421
[5]   ANALYSIS OF VONWILLEBRAND-FACTOR MULTIMERS USING A COMMERCIALLY AVAILABLE ENHANCED CHEMILUMINESCENCE KIT [J].
CUMMING, AM ;
WENSLEY, RT .
JOURNAL OF CLINICAL PATHOLOGY, 1993, 46 (05) :470-473
[6]  
FERNANDEZ MFL, 1982, BLOOD, V60, P1132
[7]   TRIPLET STRUCTURE OF VON-WILLEBRAND-FACTOR REFLECTS PROTEOLYTIC DEGRADATION OF HIGH-MOLECULAR-WEIGHT MULTIMERS [J].
FURLAN, M ;
ROBLES, R ;
AFFOLTER, D ;
MEYER, D ;
BAILLOD, P ;
LAMMLE, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (16) :7503-7507
[8]   Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis [J].
Furlan, M ;
Robles, R ;
Lammle, B .
BLOOD, 1996, 87 (10) :4223-4234
[9]   PLATELET VONWILLEBRAND-FACTOR - COMPARISON WITH PLASMA VONWILLEBRAND-FACTOR [J].
GRALNICK, HR ;
WILLIAMS, SB ;
MCKEOWN, LP ;
KRIZEK, DM ;
SHAFER, BC ;
RICK, ME .
THROMBOSIS RESEARCH, 1985, 38 (06) :623-633
[10]  
KAO KJ, 1981, BLOOD, V57, P579