tetano
Editor, Senior Moderator
Bing Du Xue Bao. 2015 Nov;31(6):629-33.
[h=1][Construction and Expression of RNase-Resisting His-Tagged Virus-Like Particles Containing FluA/B mRNA].[/h] [Article in Chinese]
Zhang J, Xue X, Xu H, Zhu K, Chen X, Zhang J, Zhang Q, Lin Y.
[h=3]Abstract[/h] To prepare virus-like particles containing FluA/B mRNA as RNA standard and control in Influenza RNA detection, the genes coding the coat protein and maturase of E. coli bacteriophage MS2 were amplified and cloned into D-pET32a vector. Then we inserted 6 histidines to MS2 coat protein by QuikChange Site-Directed Mutagenesis Kit to construct the universal expressing vector D-pET32a-CP-His. In addition, the partial gene fragments of FluA and FluB were cloned to the down-stream of expressing vector. The recombinant plasmid D-pET32a-CP-His-FluA/B was transformed to BL21 with induction by IPTG. The virus-like particles were purified by Ni+ chromatography. The virus-like particles can be detected by RT-PCR, but not PCR. They can be conserved stably for at least 3 months at both 4 degrees C and -20 degrees C. His-tagged virus-like particles are more stable and easier to purification. It can be used as RNA standard and control in Influenza virus RNA detection.
PMID: 26951007 [PubMed - in process]
[h=1][Construction and Expression of RNase-Resisting His-Tagged Virus-Like Particles Containing FluA/B mRNA].[/h] [Article in Chinese]
Zhang J, Xue X, Xu H, Zhu K, Chen X, Zhang J, Zhang Q, Lin Y.
[h=3]Abstract[/h] To prepare virus-like particles containing FluA/B mRNA as RNA standard and control in Influenza RNA detection, the genes coding the coat protein and maturase of E. coli bacteriophage MS2 were amplified and cloned into D-pET32a vector. Then we inserted 6 histidines to MS2 coat protein by QuikChange Site-Directed Mutagenesis Kit to construct the universal expressing vector D-pET32a-CP-His. In addition, the partial gene fragments of FluA and FluB were cloned to the down-stream of expressing vector. The recombinant plasmid D-pET32a-CP-His-FluA/B was transformed to BL21 with induction by IPTG. The virus-like particles were purified by Ni+ chromatography. The virus-like particles can be detected by RT-PCR, but not PCR. They can be conserved stably for at least 3 months at both 4 degrees C and -20 degrees C. His-tagged virus-like particles are more stable and easier to purification. It can be used as RNA standard and control in Influenza virus RNA detection.
PMID: 26951007 [PubMed - in process]