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作 者:何汉江[1] 汪文玉[2] 李丽华[1] 谭立志[2] 刘传爱[2] 占利生[2]
机构地区:[1]湘南学院医学部,湖南郴州423000 [2]南华大学病原生物学研究所,湖南衡阳421001
出 处:《中国热带医学》2006年第6期941-943,共3页China Tropical Medicine
基 金:湖南省卫生厅科研基金(B2004-165);湖南省郴州市科技局资助项目(04CK38)
摘 要:目的构建钩端螺旋体外膜脂蛋白Lipl21基因片段的真核表达重组质粒,利用脂质体体外转染HeLa细胞,探讨其在体外真核细胞中的表达情况,为寻找新的预防钩端螺旋体病的候选疫苗分子提供实验依据。方法应用PCR技术从钩端螺旋体黄疸出血群赖型56601株基因组模板中扩增Lipl21基因,纯化回收后克隆入pUCM-T载体,再亚克隆入真核表达载体pcDNA3·1(+),运用脂质体2000将重组体pcDNA3·1(+)/LipL21转染入HeLa细胞,免疫组化法观察目的基因的表达。结果双酶切及测序鉴定证明成功构建LipL21真核表达重组体pcDNA3·1(+)/LipL21,DNA测序显示重组质粒含有561bp的目的基因片段,读码框架正确,无碱基错配及移码突变。重组质粒pcDNA3·1(+)/LipL21在体外HeLa细胞中能有效表达目的蛋白LipL21。结论成功构建了钩端螺旋体Lipl21基因真核表达质粒pcDNA3·1(+)/Lipl21,且能够在体外真核细胞中表达,为进一步筛选新的预防钩端螺旋体病的候选疫苗分子奠定了一定的实验基础。Objective To construct the eukaryoctic expression recombinant plasmid containing the outer membrane Lipoprotein Lipl21 of the Leptospira interrogans serovar Lai, and transfect it into HeLa cells to express target protein Lipl21, to provide a new candidate antigen for preventing leptospiresis. Methods Lipl21 Gene was amplified from the genomic DNA of Leptospira interrogans serevar Lai , strain Lai 56601 by polymerase chain reaction (PCR), and the gene was inserted into cloning vector pUCm- T. The inserted IApl21 gene was subcloned into appropriate site of pcDNA3.1 ( + ) vector. The positive clones were acquired after being idenfilid with restrictive enzymes and sequence analysis. After being sequenced with DNA auto- sequence analysis instrument, The amplified DNA sequence of Lipl21 was searched for alignment with NCBI Blast program, and the recombinant plasmid was transfected into HeLa cells using Liposome. Results The target gene Lipl21 segment about 561bp was obtained successfully, cells Immunocytochemistry analysis showed that the recombinant plasmid can be expressed in HeLa cells. Conclusion The recombinant plasmid of PeDNA3.1 ( + )/Lipl21 was constructed successfully, and can be expressed in HeLa ceils, which provided the experimental basis for developing novel nucleic acid vaccine preventing leptospirosis.
分 类 号:R377.1[医药卫生—病原生物学]
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