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作者:

Xie, Q. (Xie, Q..) | Zhou, Z.-X. (Zhou, Z.-X..) (学者:周志祥) | Li, Z.-L. (Li, Z.-L..) | Zeng, Y. (Zeng, Y..)

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摘要:

An optimized recombinant HPV16 E6E7 fusion gene (HPV16 ofE6E7) was constructed according to codon usage for mammalian cell expression, and a mutant of HPV16 ofE6E7 fusion gene (HPV16 omfE6E7) was generated by site-directed mutagenesis at L57G, C113R for the E6 protein and C24G, E26G for the E7 protein for HPV16 ofE6E7 [patent pending (CN 101100672)]. The HPV16 omfE6E7 gene constructed in this work not only lost the transformation capability to NIH 3T3 cells and tumorigenicity in SCID mice, but also maintained very good stability and antigenicity. These results suggests that the HPV16 omfE6E7 gene should undergo further study for application as a safe antigen-specific therapeutic vaccine for HPV16-associated tumors. © 2011 Wuhan Institute of Virology, CAS and Springer-Verlag Berlin Heidelberg.

关键词:

E6; E7; Gene mutation; Gene optimization; Human papillomavirus (HPV); Transformation

作者机构:

  • [ 1 ] [Xie, Q.]College of Life Science and Bioengineering, Beijing University of Technology, Beijing 100124, China
  • [ 2 ] [Zhou, Z.-X.]College of Life Science and Bioengineering, Beijing University of Technology, Beijing 100124, China
  • [ 3 ] [Li, Z.-L.]College of Life Science and Bioengineering, Beijing University of Technology, Beijing 100124, China
  • [ 4 ] [Zeng, Y.]College of Life Science and Bioengineering, Beijing University of Technology, Beijing 100124, China

通讯作者信息:

  • 周志祥

    [Zhou, Z.-X.]College of Life Science and Bioengineering, Beijing University of Technology, Beijing 100124, China

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来源 :

Virologica Sinica

ISSN: 1674-0769

年份: 2011

期: 3

卷: 26

页码: 206-213

ESI学科: MICROBIOLOGY;

ESI高被引阀值:234

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WoS核心集被引频次: 0

SCOPUS被引频次: 3

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