Knecht D A, Dimond R L, Wheeler S, Loomis W F
J Biol Chem. 1984 Aug 25;259(16):10633-40.
Polyclonal antisera raised against a single lysosomal enzyme from Dictyostelium discoideum will cross-react with other lysosomal proteins due to the presence of common post-translational modification antigens. We have now isolated hybridoma cell lines secreting monoclonal antibodies that also recognize a shared lysosomal determinant. Although the same proteins are recognized by the monoclonal and polyclonal antibodies, the actual determinants differ. Also, the polyclonal serum contains antibodies which recognize at least one determinant not recognized by the monoclonal antibodies. All of the antigenic proteins are minor cell proteins but represent a majority of the proteins secreted from the cells during axenic growth. Anode-directed nonequilibrium two-dimensional gel electrophoresis of cellular and secreted protein indicates that the antigenic proteins have extremely acidic pI values; moreover, most are both sulfated and phosphorylated. Several sulfated polysaccharides, including dextran sulfate, chondroitin sulfate, and heparin inhibit binding of the monoclonal but not the polyclonal antibodies, indicating that the shared determinant recognized by the monoclonal antibodies may involve sulfated oligosaccharides. As a step in analyzing the function of the post-translational modification of lysosomal enzymes, we have screened a mutagenized population of amoeba for those lacking the antigenic determinant recognized by one of the monoclonal antibodies. Five cell lines have been isolated that completely lack the determinant. They appear to fall into at least three different classes based upon physical properties of the enzymes. One strain lacks any detectable sulfation of glycoproteins. Several of the strains are capable of forming fruiting bodies indicating that the antigenic determinant plays no crucial role in morphogenesis under laboratory conditions.
针对盘基网柄菌的一种溶酶体酶产生的多克隆抗血清,会由于存在共同的翻译后修饰抗原而与其他溶酶体蛋白发生交叉反应。我们现已分离出分泌单克隆抗体的杂交瘤细胞系,这些单克隆抗体也能识别一种共享的溶酶体决定簇。虽然单克隆抗体和多克隆抗体识别的是相同的蛋白质,但实际的决定簇有所不同。此外,多克隆血清中含有的抗体能识别至少一种单克隆抗体无法识别的决定簇。所有这些抗原性蛋白都是细胞中的次要蛋白,但在无菌培养条件下代表了细胞分泌蛋白的大部分。对细胞蛋白和分泌蛋白进行阳极导向的非平衡二维凝胶电泳表明,这些抗原性蛋白具有极低的酸性pI值;此外,大多数蛋白既被硫酸化又被磷酸化。几种硫酸化多糖,包括硫酸葡聚糖、硫酸软骨素和肝素,可抑制单克隆抗体的结合,但不抑制多克隆抗体的结合,这表明单克隆抗体识别的共享决定簇可能涉及硫酸化寡糖。作为分析溶酶体酶翻译后修饰功能的一个步骤,我们在诱变的变形虫群体中筛选了那些缺乏其中一种单克隆抗体所识别的抗原决定簇的个体。现已分离出五个完全缺乏该决定簇的细胞系。根据酶的物理性质,它们似乎至少分为三个不同的类别。一个菌株的糖蛋白没有任何可检测到的硫酸化。其中几个菌株能够形成子实体,这表明在实验室条件下,抗原决定簇在形态发生过程中不起关键作用。