Dai Wuxing, Liang Liang, Gao Hong, Huang Hailang, Chen Zhihao, Cheng Jizhong, Huangfu Yongmu
Department of Biochemistry and Molecular Biology, the School of Basic Medical Science, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
J Huazhong Univ Sci Technolog Med Sci. 2004;24(2):107-11, 123. doi: 10.1007/BF02885404.
Heat shock protein 65 (HSP65) is one of the most important protective immunogens against the tuberculosis infection. The signal sequence of antigen 85B and the whole HSP65 DNA sequence of human Mycobacterium tuberculosis (M. tuberculosis) were amplified from BCG genome and plasmid pCMV-MTHSP65 respectively by polymerase chain reactions (PCR). These two sequences were cloned into the plasmid pBCG-2100 under the control of the promoter of heat shock protein 70 (HSP70) from human M. tuberculosis, yielding the prokaryotic shuttle expression plasmid pBCG-SP-HSP65. Results of restriction endonuclease analysis, PCR detection and DNA sequencing analysis showed that the two cloned DNA sequences were consistent with those previously reported, and the direction of their inserting into the recombinant was correct and the reading frame had been maintained. The recombinants were electroporated into BCG to construct the recombinant BCG vaccine and induced by heating. The induced expression detected by SDS-PAGE showed that the content of 65 kD protein expressed in recombinant BCG was 35.69% in total bacterial protein and 74.09% in the cell lysate supernatants, suggesting that the recombinant HSP65 gene could express in BCG with high efficiency and the expressed proteins were mainly soluble. Western-blot showed that the secretive recombinant proteins could specifically combine with antibody against M. tuberculosis HSP65, indicating that the recombinant proteins possess the biological activity of HSP65.
热休克蛋白65(HSP65)是抵抗结核感染的最重要的保护性免疫原之一。分别通过聚合酶链反应(PCR)从卡介苗基因组和质粒pCMV - MTHSP65中扩增出抗原85B的信号序列和人结核分枝杆菌(结核杆菌)的全长HSP65 DNA序列。将这两个序列克隆到来自人结核杆菌的热休克蛋白70(HSP70)启动子控制下的质粒pBCG - 2100中,得到原核穿梭表达质粒pBCG - SP - HSP65。限制性内切酶分析、PCR检测和DNA测序分析结果表明,克隆的两个DNA序列与先前报道的一致,它们插入重组体的方向正确且阅读框得以保留。将重组体电穿孔导入卡介苗以构建重组卡介苗疫苗并进行加热诱导。SDS - PAGE检测诱导表达结果显示,重组卡介苗中表达的65 kD蛋白含量在总细菌蛋白中为35.69%,在细胞裂解物上清液中为74.09%,表明重组HSP65基因能在卡介苗中高效表达且表达的蛋白主要为可溶性。Western - blot显示分泌型重组蛋白能与抗结核杆菌HSP65抗体特异性结合,表明重组蛋白具有HSP65的生物学活性。