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机构地区:[1]第三军医大学西南医院整形科,重庆400038
出 处:《中华烧伤杂志》2009年第2期126-128,共3页Chinese Journal of Burns
摘 要:目的验证分泌性卷曲相关蛋白2(SFRP2)与骨母细胞特异性因子2(OSF-2)的相互作用。方法构建能在哺乳动物细胞中表达带人膜联蛋白(HA)标签的OSF-2融合蛋白重组载体pCMV—HA—OSF-2,经酶切鉴定确认后,与Myc—SFRP2重组真核表达载体pCMV-HA-SFRP2单独或共转染人HK293细胞,利用免疫共沉淀技术及蛋白质印迹法验证OSF-2与SFRP2的相互作用。结果重组载体经酶切电泳后,显示近800bp处的条带为酶切后的目的片段SFRP2编码基因,近2500bp处的条带为酶切后目的基因OSF-2。表明pCMV-Myc-SFRP2和pCMV-HA—OSF-2均构建成功。HK293细胞单独转染pCMV—Myc—SFRP2或pCMV-HA-OSF-2后,未检测到HA—OSF-2的表达;当pCMV—Myc—SFRP2和pCMV—HA,OSF-2共转染后,经Myc抗体进行免疫沉淀可见HA—OSF-2表达。结论HA—OSF-2的重组载体能在哺乳动物细胞中表达,HA—OSF-2与SFRP2间存在相互作用。Objective To verify the interaction between secreted frizzled-related protein 2 (SFRP2) and osteoblast-specific factor 2 (OSF-2). Methods HA-tagged OSF-2 fusion protein recombinant vector pCMV-HA-OSF-2, which could express in mammal ceils was constructed, then identified by enzyme-cutting and transfected into human kidney 293 (HK293) cells with or without Myc-SFRP2 recombinant eukaryotic expression vector pCMV-HA-SFRP2. The interaction between SFRP2 and OSF-2 was detected through coimmunoprecipitation and Western blotting. Results In electrophoresis bath, target fragment of SFRP2 coding gene with 800 bp and target gene OSF-2 with 2500 bp could be seen respectively after enzyme-cutting, which showed that pCMV-Myc-SFRP2 and pCMV-HA-OSF-2 were constructed successfully. No HA-OSF-2 expression was detected after pCMV-Myc-SFRP2 or pCMV-HA-OSF-2 transfection. Whereas, HA-OSF-2 expressed by Myc antibody immunoprecipitation after pCMV-Myc-SFRP2 and pCMV-HA-OSF-2 co- transfection. Conclusions HA-OSF-2 recombinant vector can express in mammal cells. Interaction exists between HA-OSF-2 and SFRP2.
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