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人肿瘤相关半乳糖基转移酶同工酶II的特性鉴定与免疫分析

Characterization and immunoassay of human tumor-associated galactosyltransferase isoenzyme II.

作者信息

Uemura M, Winant R C, Sikic B I, Brandt A E

机构信息

New Material R/D Laboratory, Konishiroku Photo Industries Co., Ltd., Tokyo, Japan.

出版信息

Cancer Res. 1988 Sep 15;48(18):5325-34.

PMID:3136919
Abstract

Galactosyltransferase (GT) (EC 2.4.1.38) was purified to homogeneity from human ovarian tumor effusion fluid and normal human serum by chromatography on alpha-lactalbumin and anti-human immunoglobulin affinity (to selectively absorb contaminating IgG) columns. Both preparations showed a single, broad band on sodium dodecyl sulfate-polyacrylamide gel electrophoresis centered at a molecular weight of 48,000, but nondenaturing polyacrylamide gel electrophoresis of GT isolated from tumor effusion fluid revealed the presence of a series of oligomeric proteins possessing GT activity, which were barely detectable in normal human serum. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of N-glycanase- and O-glycanase-treated GT revealed that each endoglycanase removed carbohydrate with an approximate molecular weight of 3,000, revealing the presence of both N-linked and O-linked oligosaccharide substitutions on GT. Purified GT (containing a mixture of GT isoenzymes) was used to immunize BALB/c mice for monoclonal antibody (MAb) preparation. Four of the MAb isolated reacted with GT. MAb 3872 (patent pending; an IgG1) was determined to be specific for a cancer-associated GT isoenzyme (GT-II) by immunostaining of Western blots and nondenaturing polyacrylamide gel electrophoresis of GT specifically eluted from a MAb 3872 affinity column. Two 125I-labeled cyanogen bromide peptides (Mr 8,400 and 7,400) prepared from 125I-GT were specifically bound and eluted from a MAb 3872 affinity column, demonstrating that the MAb 3872 GT-II-specific antigenic epitope resides on these peptides. MAb 3872 was immobilized on 1,1'-carbonyldiimidazole-activated trisacryl GF-2000 and used to specifically assay serum GT-II levels in 29 individual normal human serum samples and 77 serum samples from 38 patients with advanced ovarian tumors. The normal serum GT-II level was found to be 85.3 +/- 30.9 milliunits/ml, with a range of 17 to 160 milliunits/ml. Of the 38 tumor patients, 33 showed GT-II values in excess of 200 milliunits/ml, with a range of 216 to 8,469 milliunits/ml. Serial samples obtained from the ovarian tumor patients suggested that the serum GT-II level reflected the tumor burden of the patient.

摘要

通过在α-乳白蛋白和抗人免疫球蛋白亲和(以选择性吸收污染的IgG)柱上进行色谱分离,从人卵巢肿瘤积液和正常人血清中纯化得到了均一的半乳糖基转移酶(GT)(EC 2.4.1.38)。两种制剂在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳上均显示出一条单一的宽带,其中心分子量为48,000,但从肿瘤积液中分离的GT的非变性聚丙烯酰胺凝胶电泳显示存在一系列具有GT活性的寡聚蛋白,这些蛋白在正常人血清中几乎检测不到。用N-糖苷酶和O-糖苷酶处理的GT的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳显示,每种内切糖苷酶都去除了分子量约为3,000的碳水化合物,表明GT上存在N-连接和O-连接的寡糖取代。纯化的GT(包含GT同工酶混合物)用于免疫BALB/c小鼠以制备单克隆抗体(MAb)。分离出的4种MAb与GT反应。通过对从MAb 3872亲和柱特异性洗脱的GT进行蛋白质印迹免疫染色和非变性聚丙烯酰胺凝胶电泳,确定MAb 387(专利申请中;一种IgG1)对癌症相关的GT同工酶(GT-II)具有特异性。由125I-GT制备的两种125I标记的溴化氰肽(分子量分别为8,400和7,400)被MAb 3872亲和柱特异性结合并洗脱,表明MAb 3872的GT-II特异性抗原表位位于这些肽上。将MAb 3872固定在1,1'-羰基二咪唑活化的三丙烯酸GF-2000上,用于特异性检测29份正常人血清样本和38例晚期卵巢肿瘤患者的77份血清样本中的血清GT-II水平。发现正常血清GT-II水平为85.3±30.9毫单位/毫升,范围为17至160毫单位/毫升。在38例肿瘤患者中,33例的GT-II值超过200毫单位/毫升,范围为216至8,469毫单位/毫升。从卵巢肿瘤患者获得的数据表明血清GT-II水平反映了患者的肿瘤负荷。

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