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蓝氏贾第鞭毛虫滋养体中α18-和α12-贾第虫肌动蛋白的免疫定位

Immunolocalization of α18- and α12-giardin in Giardia lamblia trophozoites.

作者信息

Wu Sheng, Pan Weida, Shi Xianli, Abdullahi Auwalu Yusuf, Wang Zhen, Yu Xingang, Jiang Biao, Li Kangxin, Xu Chang, Li Guoqing

机构信息

Guangdong Provincial Zoonosis Prevention and Control Key Laboratory, College of Veterinary Medicine, South China Agricultural University, Guangzhou, Guangdong Province, 510642, People's Republic of China.

出版信息

Parasitol Res. 2016 Nov;115(11):4183-4187. doi: 10.1007/s00436-016-5194-z. Epub 2016 Jul 28.

Abstract

To study subcellular localization of α18- and α12-giardin in Giardia lamblia trophozoites, the α18- and α12-giardin genes were amplified from G. lamblia assemblage A, respectively. The PCR products were cloned into the prokaryotic expression vector pET-28a(+), and the positive recombinant plasmids were transformed into E. coli Rosetta (DE3) strain for the expression, and expressed α18- and α12-giardin fusion protein were purified by Ni-Agarose resin, respectively. Mice were immunized with purified fusion proteins for preparation of polyclonal antibody, and then the subcellular localization of α18- and α12-giardin was determined by fluorescence immunoassay. Results showed that the concentrations of purified α18- and α12-giardin fusion proteins were 1.20 and 0.86 mg/ml, respectively. The titers of anti-α18- and anti-α12-giardin polyclonal antibody were both as high as 1:25600 dilutions. Immunofluorescent analysis showed that α18- and α12-giardin proteins were mainly localized at four pairs of flagella and the cytoplasm of G. lamblia trophozoites, suggesting that α18- and α12-giardin are the flagella and cytoplasm-associated proteins, respectively. The above information would lay the foundation for research about the crystal structure and biological function of α18- and α12-giardin.

摘要

为研究贾第虫滋养体中α18-贾第蛋白和α12-贾第蛋白的亚细胞定位,分别从贾第虫A群中扩增α18-贾第蛋白和α12-贾第蛋白基因。将PCR产物克隆到原核表达载体pET-28a(+)中,将阳性重组质粒转化到大肠杆菌Rosetta (DE3)菌株中进行表达,并用Ni-琼脂糖树脂分别纯化表达的α18-贾第蛋白和α12-贾第蛋白融合蛋白。用纯化的融合蛋白免疫小鼠制备多克隆抗体,然后通过荧光免疫测定法确定α18-贾第蛋白和α12-贾第蛋白的亚细胞定位。结果显示,纯化的α18-贾第蛋白和α12-贾第蛋白融合蛋白浓度分别为1.20和0.86mg/ml。抗α18-贾第蛋白和抗α12-贾第蛋白多克隆抗体的效价均高达1:25600稀释度。免疫荧光分析表明,α18-贾第蛋白和α12-贾第蛋白主要定位于贾第虫滋养体的四对鞭毛和细胞质中,表明α18-贾第蛋白和α12-贾第蛋白分别是与鞭毛和细胞质相关的蛋白。上述信息将为α18-贾第蛋白和α12-贾第蛋白的晶体结构和生物学功能研究奠定基础。

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