M Paknejad, M J Rasaee, F Karami Tehrani, S Kashanian, M A Mohagheghi, K Omidfar, M Rajabi Bazl
{"title":"生产单克隆抗体PR81,识别MUC1粘蛋白串联重复区。","authors":"M Paknejad, M J Rasaee, F Karami Tehrani, S Kashanian, M A Mohagheghi, K Omidfar, M Rajabi Bazl","doi":"10.1089/153685903322286566","DOIUrl":null,"url":null,"abstract":"<p><p>A monoclonal antibody (MAb) was generated by immunizing BALB/c mice with homogenized breast cancerous tissues. This antibody (PR81) was found to be of IgG(1) class and subclass, containing kappa light chain. PR81 reacted with either the membrane extracts of several breast cancerous tissues or the cell surface of some MUC1 positive cell lines (MCF-7, BT-20 and T-47D) tested by enzyme immunoassay and for MCF-7 by immunofluorescence method. PR81 also reacted with two synthetic 27 and 16-amino acid peptides, TSA-P1-24 and A-P1-15, respectively, which included the core tandem repeat sequence of MUC1. However, this antibody did not react with a synthetic 14 amino acid peptide that has no similarity with tandem repeat found in MUC1. The generated antibody had good and similar affinities (2.19 x 10(8) M(-1)) toward TSA-P1-24 and A-P1-15, which are mainly shared in the hydrophilic sequence of PDTRPAP. Through Western blot analysis of homogenized breast tissues, PR81 recognized only a major band of 250 kDa. This band is stronger in malignant tissue than benign and normal tissues.</p>","PeriodicalId":83733,"journal":{"name":"Hybridoma and hybridomics","volume":"22 3","pages":"153-8"},"PeriodicalIF":0.0000,"publicationDate":"2003-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/153685903322286566","citationCount":"26","resultStr":"{\"title\":\"Production of monoclonal antibody, PR81, recognizing the tandem repeat region of MUC1 mucin.\",\"authors\":\"M Paknejad, M J Rasaee, F Karami Tehrani, S Kashanian, M A Mohagheghi, K Omidfar, M Rajabi Bazl\",\"doi\":\"10.1089/153685903322286566\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A monoclonal antibody (MAb) was generated by immunizing BALB/c mice with homogenized breast cancerous tissues. This antibody (PR81) was found to be of IgG(1) class and subclass, containing kappa light chain. PR81 reacted with either the membrane extracts of several breast cancerous tissues or the cell surface of some MUC1 positive cell lines (MCF-7, BT-20 and T-47D) tested by enzyme immunoassay and for MCF-7 by immunofluorescence method. PR81 also reacted with two synthetic 27 and 16-amino acid peptides, TSA-P1-24 and A-P1-15, respectively, which included the core tandem repeat sequence of MUC1. However, this antibody did not react with a synthetic 14 amino acid peptide that has no similarity with tandem repeat found in MUC1. The generated antibody had good and similar affinities (2.19 x 10(8) M(-1)) toward TSA-P1-24 and A-P1-15, which are mainly shared in the hydrophilic sequence of PDTRPAP. Through Western blot analysis of homogenized breast tissues, PR81 recognized only a major band of 250 kDa. This band is stronger in malignant tissue than benign and normal tissues.</p>\",\"PeriodicalId\":83733,\"journal\":{\"name\":\"Hybridoma and hybridomics\",\"volume\":\"22 3\",\"pages\":\"153-8\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2003-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1089/153685903322286566\",\"citationCount\":\"26\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Hybridoma and hybridomics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1089/153685903322286566\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hybridoma and hybridomics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1089/153685903322286566","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 26
摘要
用匀浆的乳腺癌组织免疫BALB/c小鼠,制备单克隆抗体(MAb)。该抗体(PR81)属IgG(1)类和亚类,含有kappa轻链。PR81与几种乳腺癌组织的膜提取物或一些MUC1阳性细胞系(MCF-7、BT-20和T-47D)的细胞表面反应,用酶免疫法检测,用免疫荧光法检测MCF-7。PR81还与合成的27和16个氨基酸的肽TSA-P1-24和A-P1-15反应,其中包括MUC1的核心串联重复序列。然而,该抗体不与合成的与MUC1中串联重复序列不相似的14个氨基酸肽反应。生成的抗体对TSA-P1-24和A-P1-15具有良好的相似亲和力(2.19 x 10(8) M(-1)),主要存在于PDTRPAP亲水性序列中。通过Western blot分析匀浆乳腺组织,PR81仅识别250 kDa的主要条带。这个波段在恶性组织中比良性和正常组织强。
Production of monoclonal antibody, PR81, recognizing the tandem repeat region of MUC1 mucin.
A monoclonal antibody (MAb) was generated by immunizing BALB/c mice with homogenized breast cancerous tissues. This antibody (PR81) was found to be of IgG(1) class and subclass, containing kappa light chain. PR81 reacted with either the membrane extracts of several breast cancerous tissues or the cell surface of some MUC1 positive cell lines (MCF-7, BT-20 and T-47D) tested by enzyme immunoassay and for MCF-7 by immunofluorescence method. PR81 also reacted with two synthetic 27 and 16-amino acid peptides, TSA-P1-24 and A-P1-15, respectively, which included the core tandem repeat sequence of MUC1. However, this antibody did not react with a synthetic 14 amino acid peptide that has no similarity with tandem repeat found in MUC1. The generated antibody had good and similar affinities (2.19 x 10(8) M(-1)) toward TSA-P1-24 and A-P1-15, which are mainly shared in the hydrophilic sequence of PDTRPAP. Through Western blot analysis of homogenized breast tissues, PR81 recognized only a major band of 250 kDa. This band is stronger in malignant tissue than benign and normal tissues.