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作 者:王珍祥[1] 袁顺宗[1] 陶熹[1] 李世荣[1] 吴军[1]
机构地区:[1]第三军医大学附属西南医院整形外科,重庆市400038
出 处:《组织工程与重建外科杂志》2009年第4期199-201,207,共4页Journal of Tissue Engineering and Reconstructive Surgery
基 金:国家重点基础研究发展规划项目(G1999054204)
摘 要:目的利用pull-down技术验证凋亡相关蛋白基因SFRP2(Secreted frizzled-related protein2)和骨母细胞特异性因子-2Periostin(Osteoblast-specific factor2)间的相互作用。方法构建能在哺乳动物细胞中表达带HA标签的Periostin融合蛋白(HA-Periostin)的重组载体pCMV-HA-Periostin,经酶切鉴定正确后,和表达带Myc标签的融合蛋白(Myc-SFRP2)的重组真核表达载体pCMV-HA-SFRP2,单独或共转染人293细胞,利用pull-down技术验证Periostin与SFRP2间的相互作用。结果成功构建重组载体pCMV-HA-Periostin,与抗Myc单克隆抗体沉淀Myc-SFRP2相互作用蛋白复合物后,可以检测到HA-Periostin的表达。通过体外蛋白质结合实验证实了Periostin与SFRP2间的相互作用。结论成功构建带HA标签的Periostin融合蛋白(HA-Periostin)的重组载体,利用pull-down技术证实了Periostin与SFRP2间的存在相互作用。Objective To investigate the interaction between Periostin (osteoblast-specifie factor 2) and SFRP 2 (Secreted frizzled-related protein 2) in the formation of keloid. Methods HA-tagged fusion protein (HA- Periostin) expression vector was constructed, identified and transfected into human embryo kidney 293 (HEK293) cells alone or with Myc-tagged fusion protein (Myc-SFRP 2) expression vector pMCV-Myc-SFRP 2. The interaction between SFRP 2 and Periostin was detected by pull-down technique. Results Double restriction enzyme digestion showed that pCMV-HA-Periostin was constructed successfully. When Myc-SFRP 2 was immunoprecipitanted, HA- Periostin was identified. And the interaction between SFRP 2 and Periostin was found by GST pull-down and His pull-down technique. Conclusion The recombinant vector pCMV-HA- Periostin was constructed successfully. The interaction between SFRP 2 and Periostin could be identified by GST pull-down and His pull-down.
关 键 词:凋亡相关蛋白基因 骨母细胞特异性因子-2 相互作用
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