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首页> 外文期刊>The biochemical journal >Development of a cleavage-site-specific monoclonal antibody for detecting metalloproteinase-derived aggrecan fragments: detection of fragments in human synovial fluids
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Development of a cleavage-site-specific monoclonal antibody for detecting metalloproteinase-derived aggrecan fragments: detection of fragments in human synovial fluids

机译:用于检测金属蛋白酶衍生的聚集蛋白聚糖片段的裂解位点特异性单克隆抗体的开发:检测人类滑液中的片段

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pWe 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 FGVGGEEDI9-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, F342-F373 and F342-D441, 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 F342-E373 product and may represent the natural physiological product of aggrecan cleaved iin vivo/i at both the MMP site (... DIPEN341 decreases F342FGVG ...) and the aggrecanase site (... ITEGE373 decreases A374RGSVI ...)./p
机译:>我们开发了一种单克隆抗体AF-28,可特异性识别具有N端FFGVG ...序列的多肽上的新表位。该序列位于已用基质金属蛋白酶(MMP)消化的聚集蛋白聚糖片段的N端。通过免疫印迹,单克隆抗体AF-28特异性检测到了用溶血素,胶原酶,明胶酶和基质溶酶消化的聚集蛋白聚糖G1-G2底物衍生的G2片段,但未能检测到从弹性蛋白酶,胰蛋白酶或组织蛋白酶B消化物中获得的G2片段。未检测到未消化的G1-G2。此外,AF-28抗体可检测到源自整个聚集蛋白聚糖的片段,并且该检测无需事先用软骨素酶或角质酶进行处理。竞争实验证实,该抗体未检测到包含内部... FFGVG ...序列的肽,而天然MMP消化的聚集蛋白聚糖片段和具有FFGVG ... N-末端的32聚体合成肽在摩尔上具有同等竞争性基础。缺少N末端苯丙氨酸残基的FFGVG 5聚体和FGVGGEEDI9聚体的竞争性分别比FFGVG ... 32聚体低50倍和230倍。用AF-28可以检测到来自球状结构域的两个片段F342-F373和F342-D441,它们是嗜中性粒细胞胶原酶消化G1-G2的预测产物,但以前未检测到。还通过蛋白质印迹分析在人滑液中检测到AF-28识别的表位。在某些患者中检测到100-200 kDa的宽带,在两名患者中发现40-60 kDa的优势带。这个小片段的大小与猪F342-E373产物的大小相对应,可能代表在两个MMP位点体内体内切割的聚集蛋白聚糖的天然生理产物(... DIPEN341降低了F342FGVG .. )和软骨聚集蛋白聚糖酶位点(... ITEGE373降低了A374RGSVI ...)。

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