...
首页> 外文期刊>Protein Expression and Purification >Preparation and characterization of fusion protein truncated Pseudomonas Exotoxin A (PE38KDEL) in Escherichia coli
【24h】

Preparation and characterization of fusion protein truncated Pseudomonas Exotoxin A (PE38KDEL) in Escherichia coli

机译:大肠杆菌中截短的假单胞菌外毒素A(PE38KDEL)融合蛋白的制备和表征

获取原文
获取原文并翻译 | 示例
           

摘要

Pseudomonas Exotoxin A (PE) and truncated PE have been used to prepare immunotoxin with monoclonal antibodies. Truncated Pseudomonas Exotoxin A (PE38KDEL) was expressed with the pET-32a(+) vector in Escherichia coli under control of a T7 promoter. The recombinant protein was purified by His-Ni2+ metal affinity chromatography and gel filtration. The biological activity of PE38KDEL was evaluated by the inhibition assay of protein synthesis in rabbit reticulocyte lysate system, and the cytotoxicity was tested in Hut102 and hepatocellular cell lines by the NITS assay. PE38KDEL can significantly inhibit luciferase synthesis in cell-free protein synthesis assay and was slightly cytotoxic in the Hut102 and hepatocellular cell lines. The results suggest that PE38KDEL would be useful for the preparation of more potent immunotoxims. (c) 2005 Elsevier Inc. All rights reserved.
机译:假单胞菌外毒素A(PE)和截短的PE已用于制备单克隆抗体的免疫毒素。截短的假单胞菌外毒素A(PE38KDEL)用pET-32a(+)载体在T7启动子的控制下在大肠杆菌中表达。通过His-Ni2 +金属亲和层析和凝胶过滤纯化重组蛋白。 PE38KDEL的生物学活性通过兔网织红细胞裂解液系统中蛋白质合成的抑制测定来评估,并且通过NITS测定在Hut102和肝细胞系中测试细胞毒性。 PE38KDEL在无细胞蛋白质合成测定中可显着抑制萤光素酶合成,并且在Hut102和肝细胞系中具有轻微的细胞毒性。结果表明,PE38KDEL可用于制备更有效的免疫毒素。 (c)2005 Elsevier Inc.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号