Johnson K J, Ward P A, Goralnick S, Osborn M J
Am J Pathol. 1977 Sep;88(3):559-74.
By a series of chromatographic procedures involving precipitation by salt, gel filtration, anionic exchange, and hydroxyapatite elution, a protein--termed the lipopolysaccharide inactivator (LPS-I)--has been isolated from normal human serum. As a result of treatment of bacterial lipopolysaccharide (LPS) by LPS-I, the treated LPS loses its toxicity for mice and reactivity in the Limulus assay and appears to be irreversibly disaggregated. The inactivation of the LPS by the purified LPS-I is temperature and time dependent and is not blocked by the addition of irreversible inhibitors of serine esterases. The LPS inactivator migrates as an alpha-globulin in whole serum and has a sedimentation velocity of approximately 4.5S. Characteristics of the inactivated LPS are briefly described using internally labeled LPS.
通过一系列包括盐沉淀、凝胶过滤、阴离子交换和羟基磷灰石洗脱的色谱程序,从正常人血清中分离出一种蛋白质——称为脂多糖灭活剂(LPS-I)。用LPS-I处理细菌脂多糖(LPS)后,处理后的LPS对小鼠失去毒性,在鲎试剂试验中失去反应性,并且似乎不可逆地解聚。纯化的LPS-I对LPS的灭活作用取决于温度和时间,并且不受丝氨酸酯酶不可逆抑制剂的添加所阻断。LPS灭活剂在全血清中作为α球蛋白迁移,沉降速度约为4.5S。使用内部标记的LPS简要描述了灭活LPS的特性。