Mercer E, Cawston T E, de Silva M, Hazleman B L
Biochem J. 1985 Nov 1;231(3):505-10. doi: 10.1042/bj2310505.
A metalloproteinase inhibitor present in human rheumatoid synovial fluid was purified by a combination of heparin-Sepharose chromatography, concanavalin A-Sepharose chromatography, ion-exchange chromatography and gel filtration. The Mr of the purified inhibitor was 28000 by SDS/polyacrylamide-gel electrophoresis and 30000 by gel filtration. The inhibitor blocked the activity of the metalloproteinases collagenase, gelatinase and proteoglycanase, but not thermolysin or bacterial collagenase. The serine proteinase trypsin was not inhibited. The inhibitory activity was lost after treatment with trypsin (0.5 micrograms/ml) at 37 degrees C for 30 min, 4-aminophenylmercuric acetate (1 mM) at 37 degrees C for 3 h, after incubation for 30 min at 90 degrees C and by reduction and alkylation. These properties suggest that the inhibitor closely resembles the tissue inhibitor of metalloproteinases ('TIMP') recently purified from connective-tissue culture medium.
采用肝素 - 琼脂糖凝胶层析、伴刀豆球蛋白A - 琼脂糖凝胶层析、离子交换层析及凝胶过滤相结合的方法,从人类风湿性滑液中纯化出一种金属蛋白酶抑制剂。经SDS / 聚丙烯酰胺凝胶电泳测定,纯化抑制剂的相对分子质量为28000,凝胶过滤法测得其相对分子质量为30000。该抑制剂可抑制金属蛋白酶胶原酶、明胶酶和蛋白聚糖酶的活性,但对嗜热菌蛋白酶或细菌胶原酶无抑制作用,对丝氨酸蛋白酶胰蛋白酶也无抑制作用。在37℃用胰蛋白酶(0.5微克/毫升)处理30分钟、37℃用对氨基苯基汞乙酸盐(1毫摩尔)处理3小时、90℃温育30分钟以及经还原和烷基化处理后,抑制活性丧失。这些特性表明,该抑制剂与最近从结缔组织培养基中纯化出的金属蛋白酶组织抑制剂(“TIMP”)极为相似。