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作 者:张新海[1] 杨琨[1] 贾卫[1] 欧阳为明[1] 刘莹[1] 许晓光[1] 李琦[1] 金伯泉[1]
机构地区:[1]第四军医大学基础医学部免疫学教研室,陕西西安710032
出 处:《细胞与分子免疫学杂志》2003年第3期288-290,共3页Chinese Journal of Cellular and Molecular Immunology
基 金:国家重点基础研究发展规划项目 (No.2 0 0 1CB51 0 0 0 4 );国家自然科学基金重点项目资助 (No.30 0 30 1 30 );国家自然科学基金资助项目 (No .39980 0 0 6)
摘 要:目的 :构建含 3C蛋白酶酶切位点的人CD2 2 6 (PTA1)分子胞膜外区Ig融合蛋白编码基因的真核表达载体 ,并进行表达和初步鉴定。方法 :将人CD2 2 6分子的胞膜外区基因 ,克隆入含 3C蛋白酶靶序列的Ig真核表达载体 p 3C Ig中。测序证实后 ,转染COS7细胞并进行瞬时表达。表达产物经亲和层析柱纯化 ,并通过免疫荧光染色及 3C蛋白酶酶切反应进行鉴定。结果 :经表达和纯化获得CD2 2 6胞膜外区的Ig融合蛋白。该融合蛋白可与表达于ECV30 4细胞表面的CD2 2 6配体有效结合。同时 ,融合蛋白的Fc段亦经 3C蛋白酶切除 ,从而获得CD2 2 6胞膜外区的真核表达分子。结论 :成功地获得了含有 3C蛋白酶酶切位点的人CD2 2 6分子胞膜外区Ig真核表达产物 ,为进一步对CD2 2 6分子进行结构和功能研究 。AIM: To construct, express and characterize the eukaryotic expression vector of encoding human CD226 (PTA1) extracellular region Ig fusion protein gene containing 3C protease restricted site. METHODS: The gene fragment encoding extracellular region of human CD226 was cloned into the eukaryotic expression vector p 3C Ig containing 3C protease restricted site and human Ig Fc fragment gene. After sequencing, the vector was transfected into COS7 cells, and the expressed molecule was purified by affinity chromatography. Finally, the product was characterized by immunofluorescent staining and 3C protease digestion. RESULTS: After expression and purification, the Ig fusion protein could bind effectively to the CD226 ligand expressed on ECV304 cells. The Fc fragment could also be cut off by 3C protease, so that the CD226 extracellular fragment was obtained. CONCLUSION: The extracellular region of human CD226 Ig fusion protein with 3C protease restricted site is expressed successfully in COS 7 cells, which lays the foundation for the structural and functional study of this molecule.
关 键 词:CD226(PTAI) 真核表达 融合蛋白 3C蛋白酶
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