Binding and detection of glycosaminoglycans immobilized on membranes treated with cationic detergents

被引:27
作者
Karlsson, M [1 ]
Edfors-Lilja, I
Björnsson, S
机构
[1] Vaxjo Univ, Dept Biosci & Proc Technol, S-35195 Vaxjo, Sweden
[2] Cent Hosp Kristianstad, Dept Clin Chem, S-29185 Kristianstad, Sweden
关键词
immobilization; membrane bound; solid phase; cationic detergent; glycosaminoglycan; proteoglycan; chondroitin sulfate; dermatan sulfate; heparan sulfate; epitopes; sequences; alcian blue; dot blot; blotting; transfer;
D O I
10.1006/abio.2000.4767
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Immobilization of molecules on surfaces is used for preparative, quantitative, and qualitative studies. Glycosaminoglycans (GAGs) are strongly hydrophilic and negatively charged molecules that do not bind well to either polystyrene surfaces or hydrophobic blotting membranes. Hydrophobic membranes were derivatized with cationic detergents to become hydrophilic and positively charged. The ability of the polyvinylidene fluoride and nitrocellulose membranes to retain GAGs increased up to 12.8 mug per spot in the dot blot assay when the membrane was treated with a cationic detergent. Immobilized GAGs were stained with alcian blue, and the staining intensity was quantitated by scanning and densitometry, The derivatized membranes were used for solid-phase extraction of GAGs in blood plasma, urine, or cerebrospinal fluid. The detection sensitivity was equal for different types of GAGs but there was a slight negative interference from fibrinogen in blood plasma. The immobilized GAGs could also be released from the membrane using a nonionic detergent at high ionic strength, Recovery of different proteoglycan populations, separated by electrophoresis and detected by reversible staining with toluidine blue, was 70-100%. (C) 2000 Academic Press.
引用
收藏
页码:51 / 58
页数:8
相关论文
共 18 条
[1]
PRECIPITATION OF POLYANIONS BY LONG-CHAIN ALIPHATIC AMMONIUM COMPOUNDS .4. ELUTION IN SALT SOLUTIONS OF MUCOPOLYSACCHARIDEQUATERNARY AMMONIUM COMPLEXES ADSORBED ON A SUPPORT [J].
ANTONOPOULOS, C ;
SCOTT, JE ;
BORELIUS, E ;
HAMNSTRO.B ;
GARDELL, S .
BIOCHIMICA ET BIOPHYSICA ACTA, 1961, 54 (02) :213-&
[2]
AOTSUKA S, 1988, CLIN EXP IMMUNOL, V73, P436
[3]
Bjornsson S, 1995, ACTA ORTHOP SCAND, V66, P158
[4]
SIZE-DEPENDENT SEPARATION OF PROTEOGLYCANS BY ELECTROPHORESIS IN GELS OF PURE AGAROSE [J].
BJORNSSON, S .
ANALYTICAL BIOCHEMISTRY, 1993, 210 (02) :292-298
[5]
SIMULTANEOUS PREPARATION AND QUANTITATION OF PROTEOGLYCANS BY PRECIPITATION WITH ALCIAN BLUE [J].
BJORNSSON, S .
ANALYTICAL BIOCHEMISTRY, 1993, 210 (02) :282-291
[6]
Quantitation of proteoglycans as glycosaminoglycans in biological fluids using an alcian blue dot blot analysis [J].
Björnsson, S .
ANALYTICAL BIOCHEMISTRY, 1998, 256 (02) :229-237
[7]
OPTIMIZATION OF AN ALCIAN BLUE DOT-BLOT ASSAY FOR THE DETECTION OF GLYCOSAMINOGLYCANS AND PROTEOGLYCANS [J].
BUEE, L ;
BOYLE, NJ ;
ZHANG, LB ;
DELACOURTE, A ;
FILLIT, HM .
ANALYTICAL BIOCHEMISTRY, 1991, 195 (02) :238-242
[8]
Evidence for the presence of a large keratan sulphate proteoglycan in the human uterine cervix [J].
Fischer, DC ;
Henning, A ;
Winkler, M ;
Rath, W ;
Haubeck, HD ;
Greiling, H .
BIOCHEMICAL JOURNAL, 1996, 320 :393-399
[9]
DETECTION BY I-125 CATIONIZED CYTOCHROME-C OF PROTEOGLYCANS AND GLYCOSAMINOGLYCANS IMMOBILIZED ON UNMODIFIED AND ON POSITIVELY CHARGED NYLON-66 [J].
HEIMER, R ;
MOLINARO, L ;
SAMPSON, PM .
ANALYTICAL BIOCHEMISTRY, 1987, 165 (02) :448-455
[10]
DETECTING PROTEOGLYCANS IMMOBILIZED ON POSITIVELY CHARGED NYLON [J].
HEIMER, R ;
SAMPSON, PM .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (02) :330-336