首页 | 本学科首页   官方微博 | 高级检索  
     


The effect of Ccnb1ip1 insulator on monoclonal antibody expression in Chinese hamster ovary cells
Authors:Rahimpour  Azam  Pourmaleki  Es’hagh  Shams   Forough  Payandeh   Zahra  Pourzardosht   Navid  Didehdar   Mojtaba  Gholami   Milad
Affiliation:1.Medical Nano-Technology & Tissue Engineering Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
;2.Department of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
;3.Department of Medical Biotechnology, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
;4.Immunology Research Center, Biomedicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran
;5.Biochemistry Department, Guilan University of Medical Sciences, Rasht, Iran
;6.Department of Medical Parasitology and Mycology, School of Medicine, Arak University of Medical Sciences, Arāk, Iran
;7.Department of Biochemistry and Genetics, School of Medicine, Arak University of Medical Sciences, Arāk, Iran
;
Abstract:Background

The increasing need for therapeutic monoclonal antibodies (mAbs) entails the development of innovative and improved expression strategies. Chromatin insulators have been utilized for the enhancement of the heterologous proteins in mammalian cells.

Methods and results

In the current study the Ccnb1ip1 gene insulator element was utilized to construct a novel vector system for the expression of an anti-CD52 mAb in Chinese hamster ovary (CHO) cells. The insulator containing (pIns-mAb) and control (pmAb) vectors were generated and stable cell pools were established using these constructs. The expression level in the cells created with pIns-mAb vector was calculated to be 233 ng/mL, and the expression rate in the control vector was 210 ng/mL, which indicated a 10.9% increase in mAb expression in pIns-mAb pool. In addition, analysis of mAb expression in clonal cells established from each pool showed a 10% increase in antibody productivity in the highest mAb producing clone derived from the pIns-mAb pool compared to the clone isolated from pmAb pool.

Conclusions

More studies are needed to fully elucidate the effects of Ccnb1ip1 gene insulator on recombinant therapeutic protein expression in mammalian cells. The combination of this element with other chromatin-modifying elements might improve its augmentation effect which could pave the way for efficient and cost-effective production of therapeutic drugs.

Keywords:
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号