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作 者:谌海兰[1] 陈曦[1] 徐绣宇[1] 谢佳瑛[1] 刘宇思[1] 赵家宁[1] 曾令斌[1] 陈特[2] 张雪梅[1] 尹一兵[1] 胥文春[1]
机构地区:[1]重庆医科大学临床检验诊断学教育部重点实验室,重庆400016 [2]重庆医科大学附属第一医院检验科,重庆400016
出 处:《临床检验杂志》2012年第11期902-905,共4页Chinese Journal of Clinical Laboratory Science
基 金:重庆市教委课题(KJ120318)
摘 要:目的通过原核表达,获得不带标签的NT-proBNP重组蛋白,并用其免疫新西兰大白兔,制备兔抗NT-proBNP抗体。方法从重组菌pET-32a(+)-NT-proBNP提取重组质粒,通过PCR扩增出目的 DNA片段,插入pCold TF载体,转化入大肠埃希菌BL21(DE3),经IPTG诱导表达融合蛋白。经镍柱亲和纯化、HRV 3C蛋白酶酶切、镍柱亲和纯化,制备不带标签的纯蛋白质,并用临床商品化试剂盒验证其抗原性。用该蛋白质免疫新西兰大白兔制备抗体,western blot鉴定其特异性。结果成功获得高纯度的不带标签的NT-proBNP蛋白,该蛋白质能被商品化的试剂盒识别。用该蛋白质免疫新西兰大白兔成功制备出高效价高特异的抗体。结论成功制备高纯度的无标签NT-proBNP蛋白及其多克隆抗体,为NT-proBNP在临床上的广泛应用奠定了基础。Objective To express tag-free N-terminal pro-B-type natriuretic peptide (NT-proBNP) by prokaryotic expression system and prepare polycolonal antibodies against the recombinant NT-proBNP. Methods NT-proBNP gene sequence was obtained from pET- 32a ( + )-NT-proBNP and inserted into pCold TF vector. The recombinant pCold TF-NT-proBNP was transferred into E. coli BI21 (DE3) and the recombinant NT-proBNP was expressed by IPTG induction. Subsequently, the recombinant NT-proBNP was purified by Nickel affinity column, and further digested with HRV 3C protease. After purification with Nickel affinity column again, tag-free recombinant NT-proBNP was obtained and its antigenicity was analyzed with the commercial kit employed in clinical test. Polyclonal antibodies against the recombinant tag-freeNT-proBNP were prepared by immunizing rabbits and the specificity of antibodies was tested by Western blot. Results Highly purified tag-free NT-proBNP protein was prepared and could be detectable by Roche NT-proBNP test kit. The polyclonal antibodies against recombinant tag-free NT-proBNP with high titer and specificity were also prepared. Conclusion Highly purified tag-free recombinant NT-proBNP protein and its specific polyclonal antibodies were successfully prepared for clinical research of NT-proBNP and widespread application in diagnosis.
关 键 词:N末端B型钠尿肽原 原核表达 蛋白质纯化 多克隆抗体
分 类 号:R541.6[医药卫生—心血管疾病]
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