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| 牛朊蛋白和酵母朊毒体结构域融合蛋白的原核表达及其单克隆抗体的制备 | |
| 引用本文： | 李炎鑫,马贵平,杨汉春,刘全国,史喜菊,李冰玲.牛朊蛋白和酵母朊毒体结构域融合蛋白的原核表达及其单克隆抗体的制备[J].畜牧兽医学报,2012,43(1):105-111. |
| 作者姓名： | 李炎鑫 马贵平 杨汉春 刘全国 史喜菊 李冰玲 |
| 作者单位： | 1. 中国农业大学动物医学院,北京100193;北京出入境检验检疫局,北京100026 2. 北京出入境检验检疫局,北京,100026 3. 中国农业大学动物医学院,北京,100193 |
| 基金项目： | 国家"十一五"科技支撑计划 |
| 摘 要： | 利用DNA重组技术将酵母Ure2p朊蛋白结构域(UPD)基因插入牛朊蛋白(BPrP)表达质粒pET-PrP中,构建原核表达载体pET-PrP-UPD.阳性质粒转化宿主菌BL21 (DE3),在IPTG诱导下获得高效表达.Westernblot检测表明表达的重组蛋白与单克隆抗体6H4呈现特异性反应,且纯化的PrP-UPD融合蛋白在体外具有聚集成淀粉样纤维、抵抗蛋白酶K消化等朊毒体的结构特点.利用纯化的PrP-UPD免疫BALB/c小鼠,取其脾细胞与SP2/0细胞融合,经克隆和筛选,获得3株稳定分泌抗重组PrP单抗的杂交瘤细胞,分别命名为1G3、3A4、4D1,其中1G3分泌的单抗能识别细胞型牛朊蛋白,其Ig亚类为IgG2b,腹水ELISA效价为1×105,Western blot表明该单抗具有较强的特异性. |
| 关 键 词： | 牛朊蛋白 酵母Ure2p朊毒体结构域 构象转变 单克隆抗体 |
Expression of a Chimera of Bovine Prion Protein and Yeast Ure2p Prion Domain in Escherichia coli and Preparation of Monoclonal Antibodies Against Prion Protein |
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| LI Yan-xin , MA Gui-ping , YANG Han-chun , LIU Quan-guo , SHI Xi-ju , LI Bing-ling.Expression of a Chimera of Bovine Prion Protein and Yeast Ure2p Prion Domain in Escherichia coli and Preparation of Monoclonal Antibodies Against Prion Protein[J].Acta Veterinaria et Zootechnica Sinica,2012,43(1):105-111. | |
| Authors: | LI Yan-xin MA Gui-ping YANG Han-chun LIU Quan-guo SHI Xi-ju LI Bing-ling |
| Institution: | 1.College of Veterinary Medicine,China Agricultural University,Beijing 100193,China; 2.Beijing Entry-exit Inspection and Quarantine Bureau,Beijing 100026,China) |
| Abstract: | The recombinant expression plasmids pET-PrP-UPD was constructed by inserting Ure2p prion domain(UPD) gene into the recombinant vector pET-PrP,The target gene was successfully expressed in the host cell BL21(DE3) when induced with IPTG.Specific reaction was found between expressed protein and monoclonal antibody 6H4 by Western blot assay.The purified PrP-UPD fusion protein was polymerized into amyloid fibrils,and exhibited partial resistance to proteinase K,Which similar to the structural characteristics of prion.The BALB/c mice were immunized with purified recombinant PrP-UPD fusion protein.Immunized splenocytes were collected and fused with SP2/0 myeloma cell line.Hybridoma culture supernatant was screened by ELISA.Three hybridoma cell lines designated 1G3,3A4 and 4D1,secreting monoclonal antibodies(mAbs) against recombinant bovine prion protein,were obtained.1G3 could secret mAbs against bovine cellar prion protein and its immunoglobulin subclasses were IgG2a.The ELISA titers of the ascites fluid were 1:10 000.The specificity of the mAb 1G3 was confirmed with Western blot. |
| Keywords: | bovine prion protein yeast Ure2p prion domin conformational conversion monoclonal antibodies |
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