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小鼠GM-CSF的基因克隆和锚定修饰
引用本文:于继云,陈兴,蔡欣,田蓉,程绍辉,许红莲,王嘉玺.小鼠GM-CSF的基因克隆和锚定修饰[J].生物技术通讯,2003,14(3):178-179.
作者姓名:于继云  陈兴  蔡欣  田蓉  程绍辉  许红莲  王嘉玺
作者单位:1. 军事医学科学院,基础医学研究所,北京,100850
2. 第四军医大学,西京医院皮肤科,西安,710032
基金项目:国家863项目(2001AA217131)
摘    要:将糖基化磷脂酰肌醇(GPI)锚定修饰的细胞因子直接转移到肿瘤细胞膜上,是研究治疗性肿瘤疫苗的一种有潜力的新策略。克隆了小鼠GM-CSF基因,井通过将从衰变加速因子(DAF)来源的GPI修饰性信号序列与mGM—CSF、嵌合,获得了GPI修饰的mGM-CSF分子,构建并鉴定了GPI锚定修饰的真核表达裁体pCI/GPI-mGM-CSF,为进一步研究表面工程治疗性肿瘤疫苗奠定了基础。

关 键 词:小鼠  GM-CSF基因  克隆  锚定修饰  肿瘤疫苗  糖基化磷脂酰肌醇  蛋白质修饰  细胞膜
文章编号:1009-0002(2003)03-0178-02
修稿时间:2003年1月10日

Cloning mouse GM-CSF and construction of GPI-anchored mGM-CSF
YU Ji-yun ,CHEN Xing ,CAI Xin ,TIAN Rong ,CHENG Shao-hui ,XU Hong-lian ,WANG Jia-xi.Cloning mouse GM-CSF and construction of GPI-anchored mGM-CSF[J].Letters in Biotechnology,2003,14(3):178-179.
Authors:YU Ji-yun  CHEN Xing  CAI Xin  TIAN Rong  CHENG Shao-hui  XU Hong-lian  WANG Jia-xi
Institution:YU Ji-yun 1,CHEN Xing 1,CAI Xin 1,TIAN Rong 2,CHENG Shao-hui 1,XU Hong-lian 1,WANG Jia-xi 1
Abstract:Direct modification of tumor cell membranes by transfer of a glycosyl-phosphatidylinositol(GPI)-anchored cytokine has been proposed as a novel potentially useful strategy to development of therapeutic tumor vaccines.In this study,mouse GM-CSF was amplified by RT-PCR using the total RNA extracted from BALB/c mouse spleen cells activated with IL-2and anti-CD3antibody in vitro.Glycosylphosphatidylinositol(GPI)-anchored variants of mGM-CSF were produced via chimerization with alternative GPI-modification signal sequences from decay-accelerat-ing factor(DAF).GPI-anchored mGM-CSF eukaryotic expression vector pCI /GPI-mGM-CSF was contracted and iso-latedand,it will may be used for research of new type therapeutic tumor vaccines.
Keywords:cancer vaccine  GM-CSF  glycosyl-phosphatidyl inositol-anchored protein  cell-surface engineering
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