Protsenko V A, Veselov V F, Protsenko A V, Kiriukhin I F, Kosik O G
Ukr Biokhim Zh (1978). 1982 Jul-Aug;54(4):377-82.
Immunochemical analysis in combination with gel filtration and isoelectric focusing made it possible to state that in blood serum of healthy people 81.3 +/- 0.5% of administered trypsin is bound with alpha 1-antitrypsin and 18.7 +/- 0.6%--with alpha 2-macroglobulin. The latter is functionally heterogeneous, only 40% of it is bound with trypsin and in the formed complex the antigenic properties of trypsin and alpha 2-macroglobulin are lost. A great number of blood serum alpha 1-antitrypsin cannot fix trypsin. The content of such alpha 1-antitrypsin rises sharply with pathology available. In the immunochemical estimation of the organism inhibitory potential relative to proteolytic enzymes not only the amount of the inhibitor but also its functional activity should be taken into account. The data of immunochemical research of the blood serum isoelectrophoregrams show that the most considerable changes under conditions of pathology occur in alpha 2-macroglobulin.
免疫化学分析结合凝胶过滤和等电聚焦表明,在健康人的血清中,所注入的胰蛋白酶有81.3±0.5%与α1-抗胰蛋白酶结合,18.7±0.6%与α2-巨球蛋白结合。后者在功能上是异质的,只有40%与胰蛋白酶结合,并且在形成的复合物中胰蛋白酶和α2-巨球蛋白的抗原特性丧失。大量血清α1-抗胰蛋白酶不能固定胰蛋白酶。这种α1-抗胰蛋白酶的含量在有病理情况时会急剧上升。在对机体相对于蛋白水解酶的抑制潜力进行免疫化学评估时,不仅要考虑抑制剂的量,还要考虑其功能活性。血清等电电泳图的免疫化学研究数据表明,在病理条件下最显著的变化发生在α2-巨球蛋白中。