Milhiet P E, Corbeil D, Simon V, Kenny A J, Crine P, Boileau G
Département de biochimie, Faculté de Médecine, Université de Montréal, Canada.
Biochem J. 1994 May 15;300 ( Pt 1)(Pt 1):37-43. doi: 10.1042/bj3000037.
Endopeptidase-24.18 (E-24.18; EC 3.4.24.18) is a metallopeptidase of the astacin family and is highly expressed in kidney brush-border membranes of rodents. Rat E-24.18 consists of two disulphide-linked alpha/beta dimers [(alpha/beta)2]. In order to investigate the mechanisms of assembly and the importance of each subunit in the enzymic process, the cloned cDNAs for the rat alpha and beta subunits were transiently expressed either alone or together in COS-1 cells. Immunoblotting of cell extracts and spent culture media showed that, when expressed alone, the alpha subunit is secreted, whereas the beta subunit is membrane-bound. In alpha/beta-transfected cells, the alpha subunit remained membrane-bound, but could be released from the cell surface after papain treatment or after incubation with 10 mM dithiothreitol. Furthermore, mutants of the alpha subunit in which the putative C-terminal anchor domain was deleted could still form cell-associated alpha/beta dimers. These results are consistent with a topological model of E-24.18 in which the beta subunit is anchored in the plasma membrane and the alpha subunit is retained at the cell surface through disulphide bridge(s) with the beta subunit. Both the alpha and beta recombinant subunits expressed in COS-1 cells showed little azocasein-degrading activity. However, activity of either individual subunits of alpha/beta dimers was increased after mild trypsin digestion, suggesting that in COS-1 cells the enzymes are synthesized as zymogens. Finally, inactivation of the alpha subunit by site-directed mutagenesis of Glu-157, which is believed to play a role in catalysis, showed that both subunits participate in the enzymic activity of the heterodimer.
内肽酶-24.18(E-24.18;EC 3.4.24.18)是一种天冬氨酸蛋白酶家族的金属肽酶,在啮齿动物的肾刷状缘膜中高度表达。大鼠E-24.18由两个通过二硫键连接的α/β二聚体[(α/β)2]组成。为了研究组装机制以及每个亚基在酶促过程中的重要性,将大鼠α和β亚基的克隆cDNA单独或一起在COS-1细胞中瞬时表达。对细胞提取物和用过的培养基进行免疫印迹分析表明,单独表达时,α亚基被分泌,而β亚基与膜结合。在α/β转染的细胞中,α亚基仍与膜结合,但在木瓜蛋白酶处理后或与10 mM二硫苏糖醇孵育后可从细胞表面释放。此外,缺失推定的C末端锚定结构域的α亚基突变体仍可形成细胞相关的α/β二聚体。这些结果与E-24.18的拓扑模型一致,即β亚基锚定在质膜中,α亚基通过与β亚基的二硫键保留在细胞表面。在COS-1细胞中表达的α和β重组亚基均显示出很少的偶氮酪蛋白降解活性。然而,α/β二聚体的任何一个亚基在轻度胰蛋白酶消化后活性都会增加,这表明在COS-1细胞中酶是以酶原形式合成的。最后,通过对被认为在催化中起作用的Glu-157进行定点诱变使α亚基失活,结果表明两个亚基都参与了异二聚体酶的活性。