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首页> 外文期刊>Molecular biology reports >Fusion expression and immunogenicity of Bordetella pertussis PTS1-FHA protein: implications for the vaccine development
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Fusion expression and immunogenicity of Bordetella pertussis PTS1-FHA protein: implications for the vaccine development

机译:百日咳博德特氏菌PTS1-FHA蛋白的融合表达和免疫原性:对疫苗开发的影响

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Mutants of pertussis toxin (PT) S1 subunit and filamentous hemagglutinin (FHA) type I immunodominant domain from Bordetella pertussis (B. pertussis) are considered to be effective candidate antigens for acellular pertussis vaccines; however, the substantial progress is hampered in part for the lack of a suitable in vitro expression system. In this paper, the gene sequences of a S1 mutant C180-R9K/E129G (mS1) and a truncated peptide named Fs from FHA type I immunodominant domain were linked together and constructed to pET22b expression vector as a fusion gene; after inducing with IPTG, it was highly expressed in E. coli BL21 (DE3) as inclusion body. The fusion protein FsmS1 was purified from cell lysates and refolded successfully. The result of Western blotting indicate that it was able to react with both anti-S1 and anti-FHA McAbs; antiserum produced from New Zealand white rabbits immunized with this protein was able to recognize both native PT and FHA antigens as determined by western blotting. These data have provided a novel feasible method to produce PT S1 subunit and FHA type I immunodominant domain in large scale in vitro, which is implicated for the development of multivalent subunit vaccines candidate against B. pertussis infection.
机译:百日咳博德特氏菌(百日咳博德特氏菌)的百日咳毒素(PT)S1亚基突变体和I型丝状血凝素(FHA)免疫优势域被认为是脱细胞百日咳疫苗的有效候选抗原。然而,由于缺乏合适的体外表达系统,部分进展受到了阻碍。本文将S1突变体C180-R9K / E129G(mS1)的基因序列与来自FHA I型免疫显性结构域的截短肽Fs连接在一起,并构建到pET22b表达载体上作为融合基因。经IPTG诱导后,它在大肠杆菌BL21(DE3)中作为包涵体高表达。从细胞裂解物中纯化出融合蛋白FsmS1,并成功重折叠。 Western blotting的结果表明它能够与抗S1和抗FHA单克隆抗体反应;用蛋白质免疫新西兰白兔产生的抗血清能够识别天然PT和FHA抗原,这是通过蛋白质印迹法确定的。这些数据为在体外大规模生产PT S1亚基和FHA I型免疫优势结构域提供了一种新颖可行的方法,与开发针对百日咳博德特氏菌感染的多价亚基疫苗有关。

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