DEVELOPMENT OF A CLEAVAGE-SITE-SPECIFIC MONOCLONAL-ANTIBODY FOR DETECTING METALLOPROTEINASE-DERIVED AGGRECAN FRAGMENTS - DETECTION OF FRAGMENTS IN HUMAN SYNOVIAL-FLUIDS

被引:84
作者
FOSANG, AJ [1 ]
LAST, K [1 ]
GARDINER, P [1 ]
JACKSON, DC [1 ]
BROWN, L [1 ]
机构
[1] UNIV MELBOURNE, DEPT MICROBIOL, PARKVILLE, VIC 3050, AUSTRALIA
关键词
D O I
10.1042/bj3100337
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have developed a monoclonal antibody AF-28 that specifically recognizes a neo-epitope on polypeptides with N-terminal FFGVG... sequences. This sequence is found at the N-terminus of aggrecan fragments that have been digested with matrix metalloproteinases (MMPs). By immunoblotting, monoclonal antibody AF-28 specifically detected G2 fragments derived from an aggrecan G1-G2 substrate digested with stromelysin, collagenase, gelatinase and matrilysin, but failed to detect G2 fragments obtained from elastase, trypsin or cathepsin B digests. Undigested G1-G2 was not detected. In addition, AF-28 antibody detected fragments derived from whole aggrecan and this detection did not require prior treatment with chondroitinase or keratanase. Competition experiments confirmed that peptides containing internal...FFGVG... sequences were not detected by the antibody, while native MMP-digested aggrecan fragments and a synthetic 32-mer peptide with FFGVG... N-termini were equally competitive on a molar basis. An FFGVG 5-mer, and an FGVGGEEDI 9-mer which lacked the N-terminal phenylalanine residue, were 50 times and 230 times respectively less competitive than the FFGVG... 32-mer. Two fragments from the interglobular domain, F-342-E(373) and F-342-D-441, that are predicted products of G1-G2 digestion by neutrophil collagenase but have not previously been detected, could be detected with AF-28. The epitope recognized by AF-28 was also detected in human synovial fluids by Western blot analysis. A broad band of 100-200 kDa was detected in some patients and a dominant band of 40-60 kDa was found in two patients. The size of this small fragment corresponds with that seen for the porcine F-342-E(373) product and may represent the natural physiological product of aggrecan cleaved in vivo at both the MMP site (... DIPEN(341)down arrow F(342)FGVG ...) and the aggrecanase site (... ITEGE(373)down arrow A(374)RGSVI...).
引用
收藏
页码:337 / 343
页数:7
相关论文
共 41 条
[1]   HYALURONAN-BINDING REGION OF AGGRECAN FROM PIG LARYNGEAL CARTILAGE - AMINO-ACID-SEQUENCE, ANALYSIS OF N-LINKED OLIGOSACCHARIDES AND LOCATION OF THE KERATAN SULFATE [J].
BARRY, FP ;
GAW, JU ;
YOUNG, CN ;
NEAME, PJ .
BIOCHEMICAL JOURNAL, 1992, 286 :761-769
[2]  
BAYLISS MT, 1989, T ORTHOP RES SOC, V14, P350
[3]  
BAYNE EK, 1994, T ORTHOP RES SOC, V19, P308
[4]  
BAYNE EK, 1995, T ORTHOP RES SOC, V20, P328
[5]   THE ACTION OF HUMAN ARTICULAR-CARTILAGE METALLOPROTEINASE ON PROTEOGLYCAN AND LINK PROTEIN - SIMILARITIES BETWEEN PRODUCTS OF DEGRADATION INSITU AND INVITRO [J].
CAMPBELL, IK ;
ROUGHLEY, PJ ;
MORT, JS .
BIOCHEMICAL JOURNAL, 1986, 237 (01) :117-122
[6]   ELECTROPHORESIS OF S-35 LABELED PROTEOGLYCANS ON POLYACRYLAMIDE-AGAROSE COMPOSITE GELS AND THEIR VISUALIZATION BY FLUOROGRAPHY [J].
CARNEY, SL ;
BAYLISS, MT ;
COLLIER, JM ;
MUIR, H .
ANALYTICAL BIOCHEMISTRY, 1986, 156 (01) :38-44
[7]  
CATERSON B, 1986, ARTICULAR CARTILAGE, P59
[8]  
DOCHERTY AJP, 1990, ANN RHEUM DIS, P469
[9]  
DOEGE KJ, 1991, J BIOL CHEM, V266, P894
[10]   ELECTROPHORETIC ANALYSIS OF MAJOR POLYPEPTIDES OF HUMAN ERYTHROCYTE MEMBRANE [J].
FAIRBANKS, G ;
STECK, TL ;
WALLACH, DFH .
BIOCHEMISTRY, 1971, 10 (13) :2606-+