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作 者:刘金明[1] 蔡学忠[1] 林矫矫[1] 杨冠珍[2] 沈小川[2] 傅志强[1] 施福恢[1] 沈纬[1] 李铭[1] 苑纯秀[1] 李浩[1] 蔡幼民 吴祥甫[2]
机构地区:[1]中国农业科学院上海家畜寄生虫病研究所,农业部动物寄生虫学重点开放试验室,上海2002322 [2]中国科学院上海生物化学研究所,上海200031
出 处:《中国寄生虫学与寄生虫病杂志》1999年第4期218-221,共4页Chinese Journal of Parasitology and Parasitic Diseases
基 金:国家科委863 高技术计划资助
摘 要:目的: 在家蚕细胞和幼虫中表达日本血吸虫脂肪酸结合蛋白( Sj14) 基因。方法: 将该基因克隆于昆虫病毒转移载体p Bac P A K His1 中, 再与修饰的家蚕核型多角体病毒( Bm N P V) 线性化 D N A 共转染家蚕细胞,经体内重组得重组病毒 Bm Sj14 , 再将 Bm Sj14 感染家蚕细胞和幼虫以表达 Sj14 , 用 Western blot 和间接 E L I S A测定表达产物的抗原性。结果: Bm Sj14 感染家蚕细胞和幼虫后 Sj14 获得较高表达; 表达产物r Sj14 ( His) 为18k Da 的融合蛋白, 在家蚕细胞中的产量约为100 μg/1 ×106 细胞, 在培养上清中产量为33 μg/ml; 在家蚕血淋巴中得量为4 mg/ml; 在家蚕幼虫组织的得量为46 mg/g 组织。 Western blot 和间接 E L I S A 显示r Sj14 ( His) 具有较高抗原性。结论: Sj14 在家蚕细胞和幼虫中获得高效表达且表达产物具有较高抗原性。AIM: To express the fatty acid binding protein ( Sj14FABP) gene of Schistosoma japonicun in the silkworm cells and larvae. METHODS: A 600 bp DNA fragment containing Sj14FABP gene was cloned into baculovirus transfer vector of pBacPAK His1 to construct recombinant transfer vector Sj14\|pBac PAK His1 . Coinfection was accomplished with this vector and Bombyx mori nuclear polyhedrosis virus (BmNPV) DNA in BmN cells. The recombinant virus of Bm\|Sj14 was screened using dot\|blotting. The BmN cells and silkworm larvae were infected with Bm\|Sj14 to express Sj14FABF gene. Western blotting and ELISA were used to identify the antigenicity of the recombinant protein. RESULTS: Sj14FABP gene was successfully expressed in the BmN cells and silkworm larvae infected with Bm\|Sj14. The product was a 18 kDa fusion protein. The yield in BmN cells was about 100 μg/1×10 6 cells and 33 μg/ml cell supernatant. In silkworm larvae, the product yield was 4 mg/ml haemolymph as well as 4\^6 mg/g silkworm tissue. The recombinant protein could be recognized by Western blotting and ELISA using the sera from mice immunized with SWAP. CONCLUSION: Sj14FABP gene has been successfully expressed in BmNPV system and the product has high antigenicity.
分 类 号:R383.24[医药卫生—医学寄生虫学]
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