Dale J B, Courtney H S, Kotb M, Schifferli D
Veterans Administration Medical Center, Memphis, Tennessee.
Infect Immun. 1990 Mar;58(3):774-8. doi: 10.1128/iai.58.3.774-778.1990.
Rabbit antisera evoked by type 5 streptococcal M protein (M5) were screened by enzyme-linked immunosorbent assay (ELISA) for immunological cross-reactivity with purified rabbit muscle phosphorylases a and b. Of 10 pep M5 antisera tested, 3 showed significant cross-reactivity with both forms of the enzyme. ELISA inhibition studies using one of the pep M5 antisera showed that all of the phosphorylase b antibodies were inhibited by pep M5, the immunogen, and phosphorylase b, the ELISA antigen. All of the antibodies were also inhibited by pep M6 and pep M19, but not by pep M24, indicating that the cross-reactive epitopes were shared by multiple serotypes of M protein. Western blot (immunoblot) analyses showed that pep M5 antisera reacted strongly with the subunit of phosphorylase b. In addition, purified phosphorylase partially inhibited the binding of pep M5 antibodies to a 95-kilodalton protein of human myocardium. One of the three cross-reactive pep M5 antisera inhibited the enzymatic activity of phosphorylase a in a dose-related fashion, reaching a maximum inhibition of 75%. The enzymatic activity in the presence of antibody was totally restored when the antiserum was first incubated with pep M5.
通过酶联免疫吸附测定(ELISA)筛选由5型链球菌M蛋白(M5)诱发的兔抗血清,以检测其与纯化的兔肌肉磷酸化酶a和b的免疫交叉反应性。在测试的10种M5抗血清中,有3种与两种形式的酶都表现出显著的交叉反应性。使用其中一种M5抗血清进行的ELISA抑制研究表明,所有磷酸化酶b抗体均被免疫原M5和ELISA抗原磷酸化酶b抑制。所有抗体也被M6和M19肽段抑制,但未被M24肽段抑制,这表明交叉反应表位为多种M蛋白血清型所共有。蛋白质印迹(免疫印迹)分析表明,M5抗血清与磷酸化酶b的亚基强烈反应。此外,纯化的磷酸化酶部分抑制了M5抗体与人心肌95千道尔顿蛋白的结合。三种具有交叉反应性的M5抗血清之一以剂量相关的方式抑制了磷酸化酶a的酶活性,最大抑制率达到75%。当抗血清首先与M5肽段孵育时,抗体存在下的酶活性完全恢复。