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结核分枝杆菌潜伏感染相关蛋白ICL的表达及鉴定 被引量:5

Expression and identification of Mycobacterium tuberculosis latent infection implicated protein ICL
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摘要 目的 表达结核分枝杆菌潜伏感染相关蛋白ICL ,鉴定其生物学活性并制备其多克隆抗体。方法 采用PCR法从结核分枝杆菌H37Rv基因组DNA中扩增出icl基因片段 ,将其插入原核表达质粒pQE30 ,构建重组质粒 pQE30 icl。将pQE30 icl转化大肠杆菌 ,用IPTG诱导目的基因表达。Western blot免疫印迹法鉴定后纯化该表达产物 ,测定其酶活性并用此纯化蛋白免疫新西兰兔制备多克隆抗体。结果 序列分析发现PCR扩得的icl有两个核苷酸突变 ,但均为无义突变。在大肠杆菌中表达的目的产物经SDS PAGE分析约为 4 7kDa。免疫印迹分析证实目的蛋白与阳性结核病患者抗血清产生特异性反应。纯化的目的蛋白异柠檬酸裂解酶的酶活性为 16 .7u/mg。双向免疫扩散法测定目的蛋白免疫兔血清的抗体效价为 1 32。结论 研制出的结核分枝杆菌重组ICL具有异柠檬酸裂解酶活性和抗原性 ,重组ICL和抗ICL免疫血清的制备为抗结核分枝杆菌潜伏感染的研究奠定了必要的物质基础。 To express and purify the Mycobacterium tuberculosis latent infection implicated protein (ICL),determine the bidogical activity and prepare the polyclonal antibody against ICL,the gene encoding ICL was amplified by PCR from genome of Mycobacterium tuberculosis H37Rv strain and inserted into prokaryotic expression vector pQE30 to obtain recombinant plasmid pQE30 icl. The recombinant vector pQE30 icl was transformed into E.coli after digestion by restriction endonuclease and sequence analysis, induced with IPTG. The product was analyzed by SDS PAGE and Western blotting. Then the expressed protein was purified by Ni NTA purification system. The enzyme activity of the purified protein was determined. The polyclonal antibody was prepared by immunization with the purified protein in New Zealand rabbits, and the specific antibody titer was determinded by double immunodiffusion.It was found that the sequence of icl obtained by PCR amplification had two nucleotides mutations,both were nonsense mutations.The expressed protein induced by IPTG in E.coli had relative molecular mass of 47 kDa. The Western blotting analysis showed the expressed protein could react with the serum from tuberculosis patients speicfically. The enzyme activity of the purified protein was 16.7u/mg. The specific antibody titer in the serum of rabbits immunized with the purified protein was 1∶32.Mycobacterium tuberculosis latent infection implicated protein ICL with enzyme activity was expressed successfully in E.coli. The polyclonal antibody of ICL was produced successfully in rabbit. Our study established some material foundations for researches against latent infection of Mycobacterium tuberculosis.
出处 《中国人兽共患病杂志》 CSCD 北大核心 2005年第1期37-40,共4页 Chinese Journal of Zoonoses
基金 国家自然科学基金资助项目 (No .3 0 2 70 5 84)
关键词 结核分枝杆菌 潜伏感染 异柠檬酸裂合酶(ICL) Mycobacterium tuberculosis latent infection isocitrate lyase
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  • 1陈全,骆旭东,蒋英,江山,朱道银.结核分枝杆菌lhp基因原核表达载体的构建和表达[J].细胞与分子免疫学杂志,2003,19(4):332-334. 被引量:4
  • 2Mitchison DA. Treatment of tuberculosis[J]. The mitchell lecture1979.J.R.Coll Physicians lond, 1980,14: 91-99. 被引量:1
  • 3Stargil-Koszycki S, Haddix PL, Russell DG. The interaction between Mycobacterium and the macrophage analyzed by two-dimensional polyacrylamide gel electrophoresis[J]. Electrophoresis, 1997,18:2558-2565. 被引量:1
  • 4Granam JE, Clark-Curtiss JE. Indentification of Mycobacterium tuberculosis RNAs synthesized in response to phagocytosis by human macrophages by selective capture of transcribed sequence(SCOTS)[J]. Proc Natl Acad Sci USA, 1999,96: 11554-11559. 被引量:1
  • 5Joseph Sambrook, David WR. In: Molecular cloning[M]. 3rd ed. Cold Spring Harbor Laboratory Press. 2001:1723-1726. 被引量:1
  • 6Floyd K, Blanc L, Ravigione M, et al. Resources required for global tuberculosis control[J]. Science, 2002, 295: 2040-2041. 被引量:1
  • 7Mckinney JD, Zu Bentrup KH, Munoz-Elias EJ, et al. Persistence of Mycobacterium tuberculosis in macrophages and mice requires the glyoxylate shunt enzyme isocitrate lyase[J]. Nature,2000,406:735-738. 被引量:1
  • 8Helmuth L. A weak link in TB bacterium is found[J]. Science,2000,289: 1123-1124. 被引量:1
  • 9Parrish NM, Dick JD, Bishai WR. Mechanisms of latency in Mycobacterium tuberculosis[J]. Trends Microbiol, 1998, 6:107-112. 被引量:1

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  • 1李俊明,朱道银,伊正君,江山,骆旭东.分枝杆菌融合表达ICL-GFP穿梭质粒的构建及鉴定[J].第四军医大学学报,2005,26(1):9-13. 被引量:2
  • 2朱中元,王海波,谢勇,陈英兰,郑冰冰,张春发,张颖.表达结核分枝杆菌融合蛋白的DNA疫苗构建及免疫保护[J].免疫学杂志,2006,22(1):47-50. 被引量:5
  • 3Floyd K, Blanc L, Ravigione M, et al. Resources required for global tuberculosis control. Science,2002,295:2040 -2041. 被引量:1
  • 4Parrish NM, Dick JD, Bishai WR. Mechanisms of latency in Mycobacterium tuberculosis. Trends Microbiol, 1998, 6 : 107-112. 被引量:1
  • 5McKinney JD, Honer zu Bentrup K, Munoz-Elias EJ, et al. Persistence of Mycobacterium tuberculosis in macrophages and mice requires the glyoxylate shunt enzyme isocitrate lyase. Nature, 2000, 406: 735-738. 被引量:1
  • 6Kaps I, Ehrt S, Seeber S, et al. Energy transfer between fluorescent proteins using a co-expression system in Mycobacterium tuberculosis. Gene,2001,278 : 115-124. 被引量:1
  • 7Li J,Zhu D,Yi Z, et al. DNAzymes targeting the icl gene inhibit ICL expression and decrease Mycobacterium tuberculosis survival in macrophage. Oligonucleotides, 2005, 15 : 215-222. 被引量:1
  • 8Chomczynski P, Sacchi N. Single step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem,1987, 162: 156-159. 被引量:1
  • 9Serrano JA, Bonete MJ. Sequencing, phylogenetic and transcriptional analysis of the glyoxylate bypass operon (ace) in the halophilic archaeon Haloferax volcanii. Biochimica Biophysica Acta, 2001, 1520: 154-162. 被引量:1
  • 10Wei J, Dalai JL, Moulder JW, et al. Identification of a Mycobacterium tuberculosis gene that enhance mycobacterial survival in macrophage. J Bacterial, 2000, 182 : 377-384. 被引量:1

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