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人类Munc18-1重组质粒的构建及蛋白表达和定位

Construction of hMunc18-1 recombinant plasmid and the expression and localization of its recombinant protein
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摘要 目的构建人类Munc18-1(hMunc18-1)真核表达质粒pEGFP-hMunc18-1并检测其融合蛋白GFPhMunc18-1在细胞内表达及定位。方法以人胎脑cDNA文库中的cDNA为模板,聚合酶链反应PCR扩增hMunc18-1全长编码基因,亚克隆至绿色荧光蛋白真核表达载体pEGFP-C1中。将构建的重组质粒pEGFPhMunc18-1送到Invitrogen公司进行基因测序,根据NCBI数据库中的hMunc18-1基因序列判断所得重组质粒的基因序列是否正确。将测序正确的质粒pEGFP-hMunc18-1转染到非洲绿猴肾细胞COS-7细胞中,提取细胞蛋白以Western blot法检测融合蛋白GFP-hMunc18-1表达,利用共聚焦激光扫描显微镜观察其在非洲绿猴肾细胞COS-7内的定位。结果 hMunc18-1全长基因序列被成功克隆到绿色荧光蛋白真核表达载体pEGFP-C1中,经酶切后鉴定其片段大小为1785bp。Western blot检测到融合蛋白GFP-hMunc18-1相对分子质量约为94 000,主要分布在细胞质,尤其是细胞膜附近。结论成功构建了hMunc18-1全长基因真核表达质粒pEGFPhMunc18-1,其融合蛋白GFP-hMunc18-1主要定位于COS-7细胞质内,尤其是细胞膜附近。 Objective To construct the recombinant plasmid pEGFP-hMunc18-1of hMunc18-1gene and identify the expression and localization of its fusion protein GFP-hMunc18-1in the cell.Methods The full-length hMunc18-1coding sequence was amplified by polymerase chain reaction(PCR)from cDNA of the human fetal brain cDNA library and was subcloned into the pEGFP-C1 vector.Then the recombinant plasmid was sequenced by the Invitrogen company,the sequencing result was determined according to hMunc18-1gene sequence in NCBI.The plasmid pEGFP-hMunc18-1with correct sequence was transfected into COS-7(African green monkey kidney)cell lines.The expression of the recombinant plasmid GFP-hMunc18-1in cells was proved by western blot method.The localization of fusion protein GFP-hMunc18-1in COS-7was observed by using laser scanning confocal microscopy.Results The full-length hMunc18-1coding sequence was successfully constructed into the expressing vector pEGFP-C1.The length of the fragment was 1785 bp which was identified by restriction enzymes digestion.The expression of GFP-hMunc18-1fusion protein was detected by western blot method,with a molecular weight of 94 000.The GFP-hMunc18-1protein was mainly localized in the cytoplasm,especially,adjacent to cell membrane.Conclusions The recombinant plasmid pEGFP-hMunc18-1 was successfully cloned into the eukaryotic expressing vector.The GFP-hMunc18-1fusion protein localized mainly in the cytoplasm of COS-7cell,especially,adjacent to cell membrane.
出处 《中国神经免疫学和神经病学杂志》 CAS 2015年第6期430-433,共4页 Chinese Journal of Neuroimmunology and Neurology
基金 辽宁省教育厅科学技术研究项目(L2013403) 沈阳医学院青年基金项目(20132028)
关键词 Munc18-1 WESTERN BLOT 绿色荧光蛋白 质粒构建 Munc18-1 Western blot GFP plasmid construction
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  • 1江基尧,张浚,李维平,徐蔚,许文辉,方乃成,罗其中,朱诚.抗癫痫药预防外伤性癫痫的多中心临床研究[J].中华神经外科疾病研究杂志,2004,3(4):301-303. 被引量:19
  • 2陈功,江澄川,程介士,杨茹.神经突触前膜胞内蛋白抗体致大鼠癫癎的机制[J].中华神经科杂志,2005,38(6):373-376. 被引量:3
  • 3Okamoto M, Sudhof TC. Munc-18-interacting proteins in synaptic vesicle exocytosis [J]. Biol Chem, 1997, 272(50) : 31459 -31464. 被引量:1
  • 4Rowe J, Calegari F, Taverna E, et al. Syntaxin 1A is delivered to the apical and basolateral domains of epithelial cells: the role of munc-18 proteins [J]. J Cell Sci, 2001, 114 (18) : 3323 -3332. 被引量:1
  • 5Yang R, Puranam RS, Butler LS, et al. Autoimmunity to mune-18 in Rasmussen's encephalitis [J]. Neuron, 2000, 28(2) : 375 -383. 被引量:1
  • 6Aarli JA. Epilepsy and the immune system [ J]. Arch Neurol, 2000, 57(12) : 1689 - 1692. 被引量:1
  • 7Palace J, Lang B. Epilepsy: an autoimmune disease? [J]. J Neurol Neurosurg Psychiatry, 2000, 69 (6) : 711 - 714. 被引量:1
  • 8Lee MC, Rho JL, Kim MK, et al. c-JUN expression and apoptotic cell death in kainate-induced temporal lobe epilepsy [ J ]. Korean Med Sci, 2001, 16(5) : 649 - 656. 被引量:1
  • 9Verhage M, Maia AS, Plomp J J, et al. Synaptic assembly of the brain in the absence of neurotransmitter secretion [ J ]. Science, 2000, 287 (5454) : 864 -869. 被引量:1
  • 10Honarpour N, Tabuchi K, Stark JM, et al. Embryonic neuronal death due to neurotrophin and neurotransmitter deprivation occurs independent of Apaf-1 [ J ]. Neuroscience, 2001, 106 (2) : 263 - 274. 被引量:1

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