杜敏,池骋,张涛,黄兰英,杨慧,国果,吴建伟,尚小丽,2021,家蝇丝氨酸蛋白酶抑制剂Serpin15的克隆表达及重组蛋白的体外活性分析[J].环境昆虫学报,(3):699-709
家蝇丝氨酸蛋白酶抑制剂Serpin15的克隆表达及重组蛋白的体外活性分析
Cloning and expression of Serpin15, a serine protease inhibitor of Musca domestica, and analysis its recombinant protein activity in vitro
  
DOI:
中文关键词:  家蝇  Serpin15基因  原核表达  抑制活性  酶稳定性
英文关键词:Musca domestica  Serpin15 gene  prokaryotic expression  in vitro activity  enzyme stability
基金项目:国家自然科学基金(A2013-14);贵州省科技合作计划(黔科合LH字[2015]7328);贵州医科大学学术新苗培养及创新探索专项(19NSP062);国家自然科学基金(81760647)
作者单位
杜敏,池骋,张涛,黄兰英,杨慧,国果,吴建伟,尚小丽 1. 贵州医科大学基础医学院现代病原生物学特色重点实验室贵阳 550025 2. 贵州医科大学生物与工程学院贵州省免疫细胞与抗体工程研究中心贵阳 550025 
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中文摘要:
      为探明家蝇重组Serpin15蛋白的体外活性和酶稳定性,本文对家蝇 Serpin15 基因进行了生物信息学分析和克隆表达,并对纯化后的家蝇重组Serpin15蛋白进行了酶特性的研究。结果显示:家蝇 Serpin15 基因ORF框全长为1 353 bp,编码450个氨基酸,理论分子量为51 076.63 Da,有信号肽和一个标志抑制活性的功能结构域RCL反应环;成功构建原核表达载体pET-28a(+)-Serpin15,经诱导表达和纯化获得家蝇重组Serpin15蛋白;重组蛋白酶特性研究发现,家蝇重组Serpin15蛋白对胰蛋白酶有极显著的抑制作用,此外,将重组Serpin15蛋白经20~60℃热处理15 min,或经pH 6~10过夜处理,或经50℃和pH 8处理后室温存放15~90 min,重组蛋白的胰蛋白酶抑制活性均仍大于70%。研究结果为家蝇Serpin15蛋白的免疫功能研究奠定了重要实验基础,也为有害昆虫杀虫剂的研发提供思路。
英文摘要:
      In order to explore the in vitro activity and enzyme stability of recombinant Serpin15 protein in Musca domestica, bioinformatics analysis, cloning and expression of Serpin15 gene of M. domestica, as well as the enzyme characteristics of recombinant Serpin15 protein were carried out. The results showed that the total length of Open Reading Frame (ORF)was 1 353 bp, encoding 450 amino acids with the theoretical molecular weight of 51 076.63 Da, a signal peptide and a reactive center loop (Serpin functional domain). The recombinant expression plasmids pET-28a(+)-Serpin15 was constructed successfully, and the recombinant Serpin15 protein was obtained by inducing expression and purification. The study of recombinant protease properties found that the recombinant Serpin15 protein had a significant inhibitory effect on trypsin. In addition, after heat-treated at 20~60℃ for 15 minutes, or overnight treatment at pH 6~10, or storage at room temperature for 15~90 min after treatment at 50℃ and pH8, the trypsin inhibitory activity of recombinant Serpin15 protein remained greater than 70%. Overall, these results laid an important foundation for future in-depth analysis the immune system of M. domestica, and also provided ideas for the development of harmful insect pesticides.
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