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机构地区:[1]山东师范大学生命科学学院,山东济南250014
出 处:《泰山医学院学报》2007年第1期22-24,共3页Journal of Taishan Medical College
摘 要:目的为深入研究叶绿体sHSP的功能,构建有效的原核表达体系,制备高特异性的叶绿体sHSP的多克隆抗体。方法将PCR方法得到的番茄叶绿体小分子热激蛋白基因(cpshsp)全长cDNA基因片段,克隆入融合表达载体pGEX6p-1中,在强启动子作用下在大肠杆菌E.coli BL21(DE3)中诱导表达,并将sHSP纯化产物免疫新西兰大白兔,western blot检测sHSP多克隆抗体。结果表达菌株经0.2 mmol/L IPTG诱导4h后,GST-CPsHSP形成包涵体,sHSP纯化产物免疫新西兰大白兔后得到叶绿体sHSP多克隆抗体,western blot检测表明该抗体的特异性和效价较好。结论构建的原核表达载体pGEX6p-1/cpshsp,在一定的诱导条件下,在DE3中得到稳定高效的融合表达,为制备叶绿体sHSP抗体提供足够的抗原,为进一步研究叶绿体sHSP的功能奠定了基础。Objective:To further study the function of the chloroplast small heat shock protein(sHSP), we inserted the gene of cpshsp of tomato into prokaryotic expression vector pGEX6p - 1 to obtain the high - specific sHSP - antibody. Methods : Recombinant protein was expressed under the control of strong promoter in strain BL21 ( DE3 ) of E. coli. The purified protein was injected into a rabbit, the specificity and effect of polyclonal antibody against sHSP were analyzed by Western Blot. Results:The chloroplast sHSP mainly existed in the form of inclusion body when the strain was induced by 0. 2mmol/LIPTG for 4 hours. The anti - sHSP polyclonal antibody was raised in the rabbit and had higher specificity and effect. Conclusion:Given appropriated conditions, the recombinant prokaryotic expression vector pGEX6p - 1/ cpshsp can express the higher specific and effective polyclonal antibody, which layed a foundation to study the function of chloroplast sHSP.
关 键 词:叶绿体小分子热激蛋白 原核表达 包涵体 多克隆抗体
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