Construction of a yeast ezpression vector of Hepatitis C Virus Non-structural 5B gene
To construct the yeast expressing HCV NS5B protein with C-terminal 21 amino acids truncated and to acquire the protein for screening the anti-HCV drugs targeting the NS5B. The coding region of HCV NS5B-C21 gene was amplified by PCR and was digested by Xho I and Not I , the gene fragment was cloned into plasmid pPICZα. The positive recombinant plasmid was obtained by identification of PCR amplification; it was named pPICZα-NS5B-C21. Emzymic hydrolysis verified that NS5B-C21 gene was correctly cloned to the vector. The successful constructing of yeast expression plasmid containing NS5B-C21 lay a better basis for carrying out further studies on establishing foundation for screening the anti-HCV drugs targeting the NS5B.
hepatitis C virus non-structural 5B gene pPICZα
Li Lin Wang Zheng-Mao Pan Ming-Jie Li Yue-Xi
Department of Epidemiology and Biostatistics, School of Public Health, Nanjing Medical University, Nanjing, 210029,China East-China Institute for Medical Biotechniques, Nanjing, 210002, China
国际会议
International Symposium on Medical and Pharmaceutical Biotechnology(医药生物技术国际研讨会)
南京
英文
58-60
2009-04-27(万方平台首次上网日期,不代表论文的发表时间)