期刊文献+

Expression of human interleukin-11 cDNA in E.coli

Expression of human interleukin-11 cDNA in E.coli
原文传递
导出
摘要 A 551-bp hIL-11 gene fragment that includes no nucleotide sequences encoding signalpolypeptide and the initial 8 amino acids of the mature protein was cloned into a high-level expression vectorpEx31B of E.coli.The authors identified the recombinant plasmid,designated pEx31-IL11,by restriction endonu-cleases digestion and DNA sequencing.The resulting recombinant plasmids were then used to transform E.colistrain HB101,and expression in the PL promoter system,which is temperature-regulated,was achieved.The ex-pressed fusion protein amounts to 50% of total bacterial proteins.The hIL-11 protein expressed in E.coliwas fused to the N-terminal 99 amino acids of the MS2 polymerase to form the inclusion body.Theserecombinant proteins can be purified to about 80% by extracting inclusion body with urea.OneIL-6-dependent cell line 7 TD1 was used for bioassay.The recombinant hIL-11 protein was preliminarily puri-fied and renatured to a specific activity of 10~5U/mg,even in the presence of an excess of a neutralizing an-ti-IL-6 antibody. A 551-bp hIL-11 gene fragment that includes no nucleotide sequences encoding signal polypeptide and the initial 8 amino acids of the mature protein was cloned into a high-level expression vector pEx31B of E.coli.The authors identified the recombinant plasmid,designated pEx31-IL11,by restriction endonu- cleases digestion and DNA sequencing.The resulting recombinant plasmids were then used to transform E.coli strain HB101,and expression in the PL promoter system,which is temperature-regulated,was achieved.The ex- pressed fusion protein amounts to 50% of total bacterial proteins.The hIL-11 protein expressed in E.coli was fused to the N-terminal 99 amino acids of the MS2 polymerase to form the inclusion body.These recombinant proteins can be purified to about 80% by extracting inclusion body with urea.One IL-6-dependent cell line 7 TD1 was used for bioassay.The recombinant hIL-11 protein was preliminarily puri- fied and renatured to a specific activity of 10~5U/mg,even in the presence of an excess of a neutralizing an- ti-IL-6 antibody.
出处 《Science China Chemistry》 SCIE EI CAS 1995年第10期1202-1209,共8页 中国科学(化学英文版)
关键词 HUMAN INTERLEUKIN-11 (hIL-11) E. COLI gene EXPRESSION fusion protein inclusion body human interleukin-11 (hIL-11) E. coli gene expression fusion protein inclusion body
  • 相关文献

参考文献12

  • 1Boquan,J.Practice of Basic Immunology. . 1991
  • 2Paul SR,Bennett F,Calvetti JA et al.Molecular cloning of a cDNA encoding interleukin 11, a stromal cell derived lymphopoietic and hematopoietic cytokine. Proceedings of the National Academy of Sciences of the United States of America . 1990
  • 3Teramura,M.,Kobayashi,S.,Hoshino,S.Interleukin-11 enhances human megakaryocytopoiesis in vitro. Blood . 1992
  • 4Schibler KR,Yang YC,Christensen RI)et al.Effect of interleukin-11 on cycling status and clonogenic maturation of fetal and adult hematopoietic progenitors. Blood . 1992
  • 5Quesniaux,V.,Clark,S. C.,Turner,K.Interleukin-II stimulates multiple phases of erythropoiesisin vitro. Blood . 1992
  • 6Baumann H,Schendel P.Interleukin-11 regulates the hepatic expression of the same plasma protein genesas interleukin-6. Journal of Biolchemistics . 1991
  • 7Kawashima,I,Ohsumi,J,Mita-Honjo,K,Shimoda-Takano,K,Ishikawa,H,Sakakibara,S,Miyadai,K,Takiguchi,Y.Molecular cloning of a cDNA encoding adipogenesis inhibitory factor and identity with interleukin-11. FEBS Letters . 1991
  • 8Cheever A W.Schistosoma haematobium: the pathology of experimental infection. Experimental Parasitology . 1985
  • 9Mosmann T.Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. Journal of Immunological Methods . 1983
  • 10Strebel K.Characterization of foot-and-mouth disease virus geneproducts with antisera against bacterially synthesized fusion proteins. Journal of Virology . 1986

共引文献9

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部