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首页> 外文期刊>Science in China, Series C. Life science >Construction of a novel fusion protein harboring mouse inter- feron gamma and epidermal growth factor receptor binding domain and enhancement of its antitumor activity
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Construction of a novel fusion protein harboring mouse inter- feron gamma and epidermal growth factor receptor binding domain and enhancement of its antitumor activity

机译:带有小鼠干扰素γ和表皮生长因子受体结合域的新型融合蛋白的构建及其抗肿瘤活性的增强

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摘要

A novel fusion protein harboring mouse interferon y and epidermal growth factor receptor binding domain was constructed with the method of genetic and protein engineering. The fusion protein kept complete antiviral activity with the liter of 10~8 IU per liter of culture. The EGF-RBD of the fusion protein exhibited competitive binding activity against ~(125)I-mEGF for mEGF receptors on A431 cells. The fusion protein was shown to be more potent in inhibiting the growth of cultured mouse breast carcinoma cells than interferon gamma. Experimental data on mouse B16 malignant melanoma model indicated that the tumor weight of fusion protein-treated group was statistically significantly smaller than that of interferon gamma-treated group. The work here provides a necessarily reliable clue for the upcoming clinical employment of a novel class of targeting inter ferons.
机译:利用遗传和蛋白质工程方法,构建了一种新型的融合蛋白,该蛋白具有小鼠干扰素和表皮生长因子受体结合域。融合蛋白保持完全的抗病毒活性,每升培养物升至10〜8 IU。融合蛋白的EGF-RBD对A431细胞上的mEGF受体表现出针对〜(125)I-mEGF的竞争性结合活性。与干扰素γ相比,该融合蛋白在抑制培养的小鼠乳腺癌细胞生长方面更有效。在小鼠B16恶性黑色素瘤模型上的实验数据表明,融合蛋白治疗组的肿瘤重量在统计学上显着小于干扰素γ治疗组的肿瘤重量。本文的工作为新型靶向干扰素的临床应用提供了必要的可靠线索。

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