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作 者:周洁 杨燕飞[1,2] 胡建华 陶凌云 高诚 ZHOU Jie YANG Yan-fei HU Jian-hua TAO Ling-yun GAO Cheng(Shanghai Research Center of Laboratory Animal, Shanghai 201203 Yangzhou University College of Veterinary, Yangzhou 225009)
机构地区:[1]上海实验动物研究中心,上海201203 [2]扬州大学兽医学院,扬州225009
出 处:《实验动物与比较医学》2016年第4期270-275,共6页Laboratory Animal and Comparative Medicine
基 金:上海市科委科技创新行动计划(13140900600),上海市科委研发平台专项(15DZ2292400)
摘 要:目的 克隆表达猴D型逆转录病毒(SRV) p27基因,评价其诊断价值.方法 PCR扩增p27基因片段,定向克隆至原核表达载体pET-28b(+),重组质粒转化大肠杆菌Rosetta (DE3)中诱导表达,利用SDS-PAGE和Western blot对表达产物进行鉴定,目的蛋白经镍柱亲和层析纯化后用ELISA方法评价其诊断价值.结果 重组质粒转化宿主菌后在37℃,异丙基-β-D-硫代半乳糖苷(IPTG)浓-度为0.5 mmol/L的条件下诱导4h,可溶性p27蛋白表达量最大,且具有免疫学活性.纯化后测定融合蛋白浓度为2.043 g/L,纯度93.3%,以融合蛋白为诊断抗原包被ELISA板检测3份标准阳性血清和22份阴性血清,检出率为100%.结论 p27基因成功表达并具有良好的反应原性,可作为猴D型逆转录病毒血清学检测的候选抗原.Objective To Clone and express p27 gene of simian type-D retrovirus and evaluate its diagnostic potential. Method Thep27 gene was amplified by RT-PCR and cloned into the prokaryotic expressive vector pET-28b(+) after sequencing. Recombinant plasmid was transformed into E.coli Rosetta DE3) and recombinant protein was analysed by SDS-PAGE and Western blot. The protein was purified affinity chromatography with Ni-NTA, and its diagnostic value was evaluated by ELISA. Results The highest soluble expression level of recombinant protein was obtained after being induced at 37 ℃ for 4 h, with the concentration of Isopropyl-β-D-thiogalactoside (IPTG) was 0.5 mmol/L, and the recombinant protein had immunological activity. After purified, the concentration of protein was 2.043 g/L, and the purity was 93.3%. The indirect ELISA was developed using the purified recombinant protein, detection of 3 standard positive sera and 22 negative sera showed the detection rate were 100%. Conclusion Recombinant p27 protein from prokaryotic expression system had perfect antigenicity, which would can be used as the candidate antigen of simian type-D retrovirus.
关 键 词:猴D型逆转录病毒 P27基因 原核表达 血清学检测
分 类 号:R373[医药卫生—病原生物学]
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